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The pelvic girdle consists of the paired hip bones (each composed of the ilium, ischium and pubis) and the sacrum. The two pubic bones articulate anteriorly at the pubic symphysis and the sacrum articulates posteriorly with the two iliac bones at the sacroiliac joint; the bones are virtually incapable of independent movement, except in the female during parturition or because of pathological change. The pelvic girdle serves as a weight-bearing and protective structure, as an attachment for trunk and lower limb muscles, and as the skeletal framework of a birth canal capable of accommodating the passage of a fetus.
The hip joint is a large synovial ball-and-socket type articulation between the head of the femur and the cup-shaped acetabulum. It permits extensive movements between the thigh and the pelvis, and between the trunk-and-pelvis (as a functional unit) and the thigh. The pivotal location of the hips serves as an essential mechanical link for many movements and postures of the body, including upright standing, locomotion, and bending toward and away from the ground.
The gluteal region or buttock is an area demarcated by the gluteal fold inferiorly, a line joining the greater trochanter and the anterior superior iliac spine laterally, the iliac crest superiorly and the midline medially. It contains a large bulk of skeletal muscle that covers several vulnerable neurovascular structures, and incorporates junctional zones between the lower limb, pelvis and perineum at the sciatic foramina. Direct and indirect musculoskeletal injuries in this region may damage the sciatic nerve and gluteal vessels.
The thigh consists of a cylinder of compact bone, the femoral shaft, surrounded by muscle groups traversed by important neurovascular structures. The muscles are grouped according to function and lie within three osteofascial compartments (anterior, posterior and medial) that are defined by fascial septa running between the femur and an enveloping tube of thick fascia, the fascia lata. The femoral artery gives off its major branch, the profunda femoris artery (deep artery of the thigh), in the anterior compartment. The sciatic nerve usually divides into its main branches, the tibial and common fibular nerves, as it passes through the posterior compartment of the thigh. The femoral nerve divides soon after entering the anterior compartment of the thigh beneath the inguinal ligament; the obturator nerve enters the medial thigh proximally and medially from the pelvis and divides into its main branches, which run anterior and posterior to adductor brevis.
See also Chapter 78 .
Most of the skin of the buttock is supplied by musculocutaneous perforating vessels from the superior and inferior gluteal arteries. There are also small peripheral contributions from similar branches of the internal pudendal, iliolumbar and lateral sacral arteries.
Cutaneous veins are tributaries of vessels that correspond to the named arteries. Cutaneous lymphatic drainage is to the superficial inguinal nodes.
The skin of the thigh distal to the inguinal ligament and gluteal fold is supplied mainly by branches of the femoral and profunda femoris arteries. There is some contribution from the obturator, inferior gluteal and popliteal arteries, and from direct cutaneous, musculocutaneous and fasciocutaneous vessels. For further details, consult .
Cutaneous veins are tributaries of vessels that correspond to the named arteries. Cutaneous lymphatic drainage is to the superficial inguinal nodes, mainly via collecting trunks accompanying the long saphenous vein.
For the dermatomes and cutaneous nerves, see Figs 76.12B , 76.13 – 76.14 .
The superficial fascia (subcutaneous tissue; tela subcutanea) of the thigh and buttock consists, as elsewhere in the limbs, of loose areolar tissue containing a variable quantity of fat. In some regions, particularly near the inguinal ligament, it splits into recognizable layers, between which may be found the branches of superficial vessels and nerves. It is thick in the inguinal region, where its two layers enclose the superficial inguinal lymph nodes, long saphenous vein and other smaller vessels. Here, the superficial layer is continuous with that of the abdominal fascia. The deep layer, a thin fibroelastic stratum, is most marked medial to the long saphenous vein and inferior to the inguinal ligament, and is interposed between the subcutaneous vessels and nerves and the deep fascia, fusing with the latter a little below the ligament. This membranous layer of subcutaneous tissue overlies the saphenous opening, blending with its circumference and with the femoral sheath. Over the opening, it is perforated by the long saphenous vein, by the superficial branches of the femoral artery other than the superficial circumflex iliac branch (which perforates the fascia lata separately), and lymphatic vessels; hence the term cribriform fascia. The subcutaneous tissue of the buttock is continuous superiorly with that over the low back and contains a variable quantity of fat.
The deep fascia (fascia musculorum) covering the gluteal muscles varies in thickness. Over gluteus maximus it is thin, but over the anterior two-thirds of gluteus medius it forms the thick, strong gluteal aponeurosis. This is attached to the lateral border of the iliac crest superiorly, and splits anteriorly to enclose tensor fasciae latae and posteriorly to enclose gluteus maximus.
The fascia lata, the expansive deep fascia that surrounds the thigh, is thicker in the proximal and lateral parts of the thigh where tensor fasciae latae and an expansion from gluteus maximus are attached to it. It is thin posteriorly and over the adductor muscles, but thicker around the knee, where it is strengthened by expansions from the tendon of biceps femoris laterally, sartorius medially and quadriceps femoris anteriorly. The fascia lata is attached superiorly and posteriorly to the back of the sacrum and coccyx, laterally to the outer margin of the iliac crest, anteriorly to the inguinal ligament, the iliac fascia and superior ramus of the pubis, and medially to the inferior ramus of the pubis, the ramus and tuberosity of the ischium, and the lower border of the sacrotuberous ligament. From the iliac crest, it descends as a dense layer over gluteus medius to the upper border of gluteus maximus, where it splits into two layers, one passing superficial and the other deep to the muscle, the layers reuniting at the lower border of the muscle.
Over the flattened lateral surface of the thigh the fascia lata thickens to form a strong band, the iliotibial tract. The upper end of the tract splits into two layers, where it encloses and anchors tensor fasciae latae and receives, posteriorly, most of the tendon of gluteus maximus. The superficial layer ascends lateral to tensor fasciae latae to the iliac crest; the deeper layer passes up and medially, deep to the muscle, and blends with the lateral part of the capsule of the hip joint. Distally the iliotibial tract is attached to a smooth, triangular facet (Gerdy’s tubercle) on the anterolateral aspect of the lateral condyle of the tibia, where it is superficial to, and blends with, an aponeurotic expansion from vastus lateralis. When the knee is extended against resistance, it stands out as a strong, visible ridge on the anterolateral aspect of the thigh and knee.
Distally the fascia lata is attached to all exposed bony points around the knee joint, such as the condyles of the femur and tibia, and the head of the fibula. On each side of the patella the deep fascia is reinforced by transverse fibres, which receive contributions from the lateral and medial vasti. The stronger lateral fibres are continuous with the iliotibial tract.
The deep surface of the fascia lata yields two intermuscular septa, which are attached to the whole of the linea aspera of the posterior femur and to its proximal and distal prolongations. The lateral septum, thicker and stronger than the medial one, extends from the attachment of gluteus maximus to the lateral femoral condyle; it lies between vastus lateralis in front and the short head of biceps femoris behind, and provides partial attachment for them. The medial, thinner and weaker septum lies between vastus medialis and the adductors and pectineus. Numerous smaller septa, such as that separating the thigh adductors and flexors, pass between the individual muscles, ensheathing them and sometimes providing partial attachment for their fibres.
The saphenous opening is an aperture in the deep fascia, inferolateral to the medial end of the inguinal ligament, which allows passage for the long saphenous vein and other smaller vessels ( Fig. 77.1 ). The cribriform fascia, which is pierced by these structures, fills in the aperture and must be removed to reveal it. Adjacent subsidiary openings may exist to transmit venous tributaries. In the adult, the approximate centre of the saphenous opening is 3 cm lateral to a point just distal to the pubic tubercle. The length and width of the opening vary considerably. The fascia lata in this part of the thigh displays superficial and deep strata (not to be confused with the superficial and deep layers of the subcutaneous tissue described above). They lie, respectively, anterior and posterior to the femoral sheath, with the saphenous opening situated where the two layers are in continuity. This serves to explain the somewhat oblique and spiral configuration of the saphenous opening.
The superficial layer, lateral and superior to the saphenous opening, is attached, in continuity, to the crest and anterior superior spine of the ilium, to the whole length of the inguinal ligament, and to the pecten pubis and lacunar ligament. It is reflected inferolaterally from the pubic tubercle as the arched falciform margin, which forms the superior, lateral and inferior boundaries of the saphenous opening; this margin adheres to the anterior layer of the femoral sheath, and the cribriform fascia is attached to it. The falciform margin is considered to have superior and inferior horns. The inferior horn is well defined, and is continuous behind the long saphenous vein with the deep stratum of the fascia lata.
The deep layer is medial to the saphenous opening and is continuous with the superficial stratum at its lower margin. Traced upwards, it covers pectineus, adductor longus and gracilis, passes behind the femoral sheath, with which it blends, and continues to the pecten pubis.
The femoral sheath is a funnel-shaped distal prolongation of extraperitoneal fascia, formed of transversalis fascia anterior to the femoral vessels, and of the iliac fascia posteriorly. It is wider proximally and its tapered distal end fuses with the vascular adventitia 3 or 4 cm distal to the inguinal ligament. At birth the sheath is shorter; it elongates when extension at the hips becomes habitual. The femoral branch of the genitofemoral nerve perforates its lateral wall. The medial wall slopes laterally and is pierced by the long saphenous vein and lymphatic vessels. Like the carotid sheath, the femoral sheath encloses a mass of connective tissue in which the vessels are embedded. Three compartments are described: a lateral compartment containing the femoral artery; an intermediate one for the femoral vein; and a medial compartment, the femoral canal, which contains lymph vessels and an occasional lymph node embedded in areolar tissue. The presence of this canal allows the femoral vein to distend. The canal is conical and approximately 1.25 cm in length. Its proximal (wider) end, termed the femoral ring, is bounded in front by the inguinal ligament, behind by pectineus and its fascia and the pectineal ligament, medially by the crescentic, lateral edge of the lacunar ligament and laterally by the femoral vein. The spermatic cord, or the round ligament of the uterus, is just above its anterior margin, while the inferior epigastric vessels are near its anterolateral rim. It is larger in women than in men: this is due partly to the relatively greater width of the female pelvis and partly to the smaller size of the femoral vessels in women. The ring is filled by condensed extraperitoneal tissue, the femoral septum, which is covered on its proximal aspect by the parietal peritoneum. Numerous lymph vessels that connect the deep inguinal to the external iliac lymph nodes traverse the femoral septum ( Fig. 77.2 ).
Femoral hernia is described with other groin hernias in Chapter 60 .
The iliac fascia covers psoas and iliacus. It is thin above but thickens progressively towards the inguinal ligament. The part covering psoas is thickened above as the medial arcuate ligament. Medially the fascia over psoas is attached by a series of fibrous arches to the intervertebral discs, the margins of vertebral bodies and the upper part of the sacrum. Laterally, it blends with the fascia anterior to quadratus lumborum above the iliac crest, and with the fascia covering iliacus below the crest. The iliac part is connected laterally to the whole of the inner lip of the iliac crest and medially to the pelvic brim, where it blends with the periosteum. At approximately the height of the anterior superior iliac spine, the iliac fascia forms an open, curved superior edge, known as the iliopectineal arch (see Fig. 77.1 ). This arch passes directly over the femoral nerve, and iliacus and psoas major. The medial extent of the arch is attached to the iliopubic ramus, where it receives a slip from the tendon of psoas minor, when this muscle is present ( ). The external iliac vessels are anterior to the fascia but the branches of the lumbar plexus are posterior to it. The fascia is separated from the peritoneum by loose extraperitoneal tissue. Lateral to the femoral vessels the iliac fascia is continuous with the posterior margin of the inguinal ligament and the transversalis fascia. Medially, it passes behind the femoral vessels to become the pectineal ligament, attached to the pecten pubis. At the junction of its lateral and medial parts, it is attached to the iliopubic ramus and the capsule of the hip joint. It thus forms a septum between the inguinal ligament and the hip bone, dividing the space here into a lateral part, the muscular space, containing psoas major, iliacus and the femoral nerve, and a medial part, the vascular space, transmitting the femoral vessels (see Fig. 77.2 ). The iliac fascia continues downwards to form the posterior wall of the femoral sheath.
The obturator membrane ( Fig. 77.3 ; see Fig. 77.2A ) is a thin aponeurosis that closes (obturates) most of the obturator foramen, leaving a superolateral aperture, the obturator canal, through which the obturator vessels and nerve leave the pelvis and enter the thigh. The membrane is attached to the sharp margin of the obturator foramen except at its inferolateral angle, where it is fixed to the pelvic surface of the ischial ramus, i.e. internal to the foramen. Its fibres are arranged mainly transversely in interlacing bundles; the uppermost bundle, which is attached to the obturator tubercles, completes the obturator canal. The outer and inner surfaces of the obturator membrane provide attachment for the obturator externus and internus, respectively. Some fibres of the pubofemoral ligament of the hip joint are attached to the outer surface.
The relevant bones in this region include the pelvic girdle (which consists of two hip bones, sacrum and coccyx) and the two femurs.
The hip bone is large, irregular, constricted centrally and expanded above and below ( Figs 77.4 – 77.5 ). Its lateral surface has a deep, cup-shaped acetabulum, articulating with the femoral head, anteroinferior to which is the large, oval or triangular obturator foramen. Above the acetabulum, the bone widens into an undulant plate surmounted by a sinuously curved iliac crest. The bone articulates in front with its fellow and posteriorly with the sacrum to form the pelvic girdle. Each hip bone has three parts, ilium, ischium and pubis, connected to each other by cartilage in youth but united as one bone in adults. The principal union is in the acetabulum. The ilium includes the upper acetabulum and expanded area above it; the ischium includes the posteroinferior acetabulum and bone posteroinferior to it; the pubis forms the anteroinferior acetabulum.
The acetabulum (see Fig. 77.4A ) is an approximately hemispherical cavity situated about the centre of the lateral aspect of the hip bone. It faces anteroinferiorly and is circumscribed by an irregular margin deficient inferiorly at the acetabular notch. The acetabular fossa forms the central floor and is rough and non-articular. The articular lunate surface is widest above (the ‘dome’), where weight is transmitted to the femur. Consequently, fractures through this region tend to be associated with unsatisfactory outcomes. All three components of the hip bone contribute to the acetabulum, although unequally. The pubis forms the anterosuperior fifth of the articular surface, the ischium forms the floor of the fossa and rather more than the posteroinferior two-fifths of the articular surface, and the ilium forms the remainder.
The obturator foramen lies below and slightly anterior to the acetabulum, between the pubis and ischium. It is bordered above by the grooved obturator surface of the superior pubic ramus, medially by the pubic body and its inferior ramus, below by the ischial ramus, and laterally by the anterior border of the ischial body, including the margin of the acetabulum. It is almost closed by the obturator membrane, which is attached to its margins, except superolaterally, where a communication remains between the pelvis and thigh. This free edge of the membrane is attached to an anterior obturator tubercle at the anterior end of the inferior border of the superior pubic ramus, and a posterior obturator tubercle on the anterior border of the acetabular notch; these tubercles are sometimes indistinct. The foramen is large and oval in males, but smaller and nearly triangular in females.
The thicker parts of the hip bone are trabecular, encased by two layers of compact bone, while the thinner parts, as in the acetabulum and central iliac fossa, are often translucent and consist of a single lamina of compact bone. In the upper acetabulum and along the arcuate line, i.e. the route of weight transmission from the sacrum to the femur, the amount of compact bone is increased and the subjacent trabecular bone displays two sets of pressure lamellae. These start together near the upper auricular surface and diverge to meet two strong buttresses of compact bone, from which two similar sets of lamellar arches start and converge on the acetabulum. The anterior part of the iliac crest has been much studied with regard to distribution of cortical and trabecular bone. described the cortical bone as very porous, being only 75% bone, decreasing to 35% near the anterior superior iliac spine.
Studies of the internal stresses within the hip bone have revealed a pattern of trabeculae that corresponds well with the theoretically expected patterns of stress trajectories ( ). These patterns are considerably more complex than in any other major bone. Stresses are higher in the acetabular than in the iliac region. In the ilium, the pelvic surface is subjected to considerably less stress than is the gluteal surface.
See individual bones.
In the infant, nutrient arteries are clearly demonstrable for each component of the hip bone. Each nutrient artery branches in a fan-like fashion within its bone of supply ( ). Later, a periosteal arterial network develops, with contributions from numerous local arteries (see under individual bones).
Periosteal innervation is by a network of nerves derived from branches of local nerves. These nerves also supply muscles attaching to the periosteum and the joints involving the hip bone. Autonomic nerves accompany nutrient arteries and branch within the bone.
Ossification ( Figs 77.6 – 77.7 ) is by three primary centres: one each for the ilium, ischium and pubis. The iliac centre appears above the greater sciatic notch prenatally at about postmenstrual weeks 9–10; the ischial centre in its body during postmenstrual weeks 13–16; and the pubic centre in its superior ramus during postmenstrual weeks 13–20. The pubis is often not recovered from prenatal remains due to its size and fragility and because it is the last of the hip bones to begin ossification ( ). At birth the whole iliac crest, the acetabular floor and the inferior margin are cartilaginous. Gradual ossification of the three components of the acetabulum results in a triradiate cartilaginous stem extending medially to the pelvic surface as a Y-shaped epiphysial plate between the ilium, ischium and pubis, and including the anterior inferior iliac spine. Cartilage along the inferior margin also covers the ischial tuberosity, forms conjoined ischial and pubic rami, and continues to the pubic symphysial surface and along the pubic crest to the pubic tubercle.
FLOAT NOT FOUND
The ossifying ischium and pubis fuse to form a continuous ischiopubic ramus at the seventh or eighth year. Secondary centres, other than for the acetabulum, appear at about puberty and fuse between the fifteenth and twenty-fifth years. There are usually two for the iliac crest (which fuse early), and single centres for the ischial tuberosity (in cartilage close to the inferior acetabular margin and spreading forwards), anterior inferior iliac spine (although it may ossify from the triradiate cartilage) and symphysial surface of the pubis (the pubic tubercle and crest may have separate centres). Progression of ossification of the iliac crest in girls is an index of skeletal maturity and is useful in determining the optimal timing of surgery for spinal deformity.
Between the ages of 8 and 9 years, three major centres of secondary ossification appear in the acetabular cartilage. The largest appears in the anterior wall of the acetabulum and fuses with the pubis, the second in the iliac acetabular cartilage superiorly, fusing with the ilium, and the third in the ischial acetabular cartilage posteriorly, fusing with the ischium. At puberty, these epiphyses expand towards the periphery of the acetabulum and contribute to its depth ( ). Fusion between the three bones within the acetabulum occurs between the sixteenth and eighteenth years. have suggested that ossification of the ilium is similar to that of a long bone, possessing three cartilaginous epiphyses and one cartilaginous process, although it tends to undergo osteoclastic resorption comparable with that of cranial bones. During development the acetabulum increases in breadth at a faster rate than it does in depth.
Avulsion fractures of pelvic apophyses may occur from excessive pull on tendons, usually in athletic adolescents. The most frequent examples of such injuries are those to the ischial tuberosity (hamstrings) and anterior inferior iliac spine (rectus femoris).
The pubis (see Figs 77.4 – 77.5 ) is the ventral part of the hip bone and forms a median cartilaginous pubic symphysis with its fellow. The body of the pubis occupies the anteromedial part of the bone, and from the body a superior ramus passes up and back to the acetabulum and an inferior ramus passes back, down and laterally to join the ischial ramus inferomedial to the obturator foramen.
The body, anteroposteriorly compressed, has anterior, posterior and symphysial (medial) surfaces and an upper border, the pubic crest. The anterior surface also faces inferolaterally; it is rough superomedially and smooth elsewhere, giving attachment to medial thigh muscles. The smooth posterior surface faces upwards and backwards as the oblique anterior wall of the lesser pelvis and is related to the urinary bladder. The symphysial surface is elongated and oval, united by cartilage to its fellow at the pubic symphysis. Denuded of cartilage, it has an irregular surface of small ridges and furrows or nodular elevations, varying considerably with age, features that are of forensic interest. The pubic crest is the rounded upper border of the body and overhangs the anterior surface; the pubic tubercle is a small rounded eminence on its lateral end. Both crest and tubercle are palpable; the latter partly is obscured in males by the spermatic cord that crosses above it from the scrotum to the anterior abdominal wall. The pubic rami diverge posterolaterally from the superolateral corners of the body.
The anterior surface of the pubic body faces the adductor region. The anterior pubic ligament attaches to its medial part along a rough strip, which is wider in females. The posterior surface is separated from the urinary bladder by retropubic fat. The puboprostatic ligaments are attached to this surface medial to levator ani.
The superior pubic ramus passes upwards, backwards and laterally from the body, superolateral to the obturator foramen, to reach the acetabulum. It is triangular in section and has three surfaces and borders. Its anterior, pectineal surface, tilted slightly up, is triangular in outline and extends from the pubic tubercle to the iliopubic ramus. It is bounded in front by the rounded obturator crest and behind by the sharp pecten pubis (pectineal line), which, with the crest, is the pubic part of the linea terminalis (i.e. anterior part of the pelvic brim). The posterosuperior, pelvic surface, medially inclined, is smooth and narrows into the posterior surface of the body, which is bounded above by the pecten pubis and below by a sharp inferior border. The obturator surface, directed down and back, is crossed by the obturator groove sloping down and forwards. Its anterior limit is the obturator crest and its posterior limit is the inferior border.
The inferior pubic ramus, an inferolateral process of the body, descends inferolaterally to join the ischial ramus medial to, and below, the obturator foramen. The union may be locally thickened, but not obviously so in adults. The ramus has two surfaces and borders. The anterolateral surface, continuous above with that of the pubic body, faces the thigh and is marked by muscles. It is limited laterally by the margin of the obturator foramen, and medially by the rough anterior border. The posteromedial surface is continuous above with that of the body and is transversely convex; its medial part is often everted in males and gives attachment to the crus of the penis. This surface faces the perineum medially, its smooth lateral part tilted up towards the pelvic cavity.
The internal surface is indistinctly divided into medial, intermediate and lateral areas. The medial area faces inferomedially in direct contact with the crus of the penis or clitoris and is limited above and behind by an indistinct ridge for attachment of the fascia overlying the superficial perineal muscles. The medial margin of the ramus, strongly everted in males, provides attachment for the fascia lata and the stratum membranosum perinei.
The pubic tubercle provides attachment to the medial end of the inguinal ligament. It forms part of the floor of the superficial inguinal ring and is crossed by the spermatic cord.
The pecten pubis is the sharp, superior edge of the pectineal surface. The conjoint tendon (inguinal falx) and lacunar ligament are attached at its medial end and a strong, fibrous pectineal ligament is attached along the rest of its surface. The smooth pelvic surface is separated from parietal peritoneum only by areolar tissue, in which the lateral umbilical ligament descends forwards across the ramus and, laterally, the vas ductus deferens (vas deferens) passes backwards. The obturator groove, which is converted to a canal by the upper borders of the obturator membrane and obturator muscles, transmits the obturator vessels and nerve from the pelvis to the thigh. Some fibres of the pubofemoral ligament are attached to the lateral end of the obturator crest.
The tendon of adductor longus is attached on the anterior (external) surface of the body, below the pubic crest. Below adductor longus, gracilis is attached to a line near the lower margin extending down on to the inferior ramus. Above gracilis, adductor brevis is attached to the body and inferior ramus. Above again, obturator externus is attached to the anterior surface, spreading on to the inferior pubic and ischial rami. Adductor magnus usually extends from the ischial ramus on to the lower part of the inferior pubic ramus between adductor brevis and obturator externus. Pectineus is attached to the pectineal surface of the superior ramus along its upper part. Ascending loops of cremaster are attached to the pubic tubercle. The lateral part of rectus abdominis and, inferiorly, pyramidalis, are attached lateral to the tubercle, on the pubic crest. Medially, the crest is crossed by the medial part of rectus abdominis, ascending from ligamentous fibres that interlace in front of the pubic symphysis. Anterior fibres of levator ani are attached on the posterior (internal) surface of the body near its centre. More laterally, obturator internus is attached on this surface, extending on to both rami. Psoas minor, when present, is attached near the centre of the pecten pubis ( ).
The pubis is supplied by a periosteal anastomosis of branches from the obturator, inferior epigastric and medial circumflex femoral arteries. The superficial and deep external pudendal arteries may also contribute. Multiple vascular foramina are present, mainly at the lateral (acetabular) end of the bone, but there is no consistently placed nutrient foramen.
The pubic periosteum is innervated by branches of the nerves that supply muscles attached to the bone, the hip joint and the symphysis pubis.
Ossification of the pubis is described on page 1355 .
The ilium has upper and lower parts and three surfaces (see Figs 77.4 – 77.5 ). The smaller, lower part forms a little less than the upper two-fifths of the acetabulum. The upper part is much expanded, and has gluteal, sacropelvic and iliac (internal) surfaces. The posterolateral gluteal surface is an extensive rough area; the anteromedial iliac fossa is smooth and concave; and the sacropelvic surface is medial and posteroinferior to the fossa, from which it is separated by the medial border.
The iliac crest is the superior border of the ilium. It is convex upwards but sinuous from side to side, being internally concave in front and convex behind. Its ends project as anterior and posterior superior iliac spines. The anterior superior iliac spine is palpable at the lateral end of the inguinal fold; the lateral end of the inguinal ligament is attached to the anterior superior iliac spine. The posterior superior iliac spine is not easily palpable but is often indicated by a dimple, approximately 4 cm lateral to the second sacral spinous process, above the medial gluteal region.
The iliac crest has ventral and dorsal segments. The ventral segment occupies slightly more than the anterior two-thirds of the iliac crest and its prominence is associated with changes in iliac form as a result of the emergence of the upright posture. It has internal and external lips and a rough intermediate zone that is narrowest centrally. The dorsal segment, which occupies approximately the posterior one-third in humans, is a feature of all land vertebrates. It has two sloping surfaces separated by a longitudinal ridge ending at the posterior superior spine. The interosseous and posterior sacroiliac ligaments arise from the medial margin of the dorsal segment. The tubercle of the iliac crest projects outwards from the outer lip approximately 5 cm posterosuperior to the anterior superior spine. The summit of the iliac crest, a little behind its midpoint, is level with the fourth lumbar vertebral body in adults and with the fifth lumbar vertebral body in children aged 10 years or less ( ).
The anterior border descends to the acetabulum from the anterior superior spine. Superiorly, it is concave forwards. Inferiorly, immediately above the acetabulum, is a rough anterior inferior iliac spine, which is divided indistinctly into an upper area for the straight head of rectus femoris and a lower area extending laterally along the upper acetabular margin to form a triangular impression for the proximal end of the iliofemoral ligament.
The posterior border is irregularly curved and descends from the posterior superior spine, at first forwards, with a posterior concavity forming a small notch. At the lower end of the notch is a wide, low projection: the posterior inferior iliac spine. Here the border turns almost horizontally forwards for approximately 3 cm, then down and back to join the posterior ischial border. Together these borders form a deep notch, the greater sciatic notch, which is bounded above by the ilium and below by the ilium and ischium. The upper fibres of the sacrotuberous ligament are attached to the upper part of the posterior border. The superior rim of the notch is related to the superior gluteal vessels and nerve. The lower margin of the greater sciatic notch is covered by piriformis and is related to the exiting sciatic nerve.
The medial border separates the iliac fossa and the sacropelvic surface. It is indistinct near the crest, rough in its upper part, then sharp where it bounds an articular surface for the sacrum, and finally rounded. The latter part is the arcuate line, which inferiorly reaches the posterior part of the iliopubic ramus, marking the union of the ilium and pubis.
The gluteal surface, facing inferiorly in its posterior part and laterally and slightly downwards in front, is bounded above by the iliac crest, and below by the upper acetabular border and by the anterior and posterior borders. It is rough and curved, convex in front, concave behind and marked by three gluteal lines. The posterior gluteal line is shortest, descending from the external lip of the crest approximately 5 cm in front of its posterior limit and ending in front of the posterior inferior iliac spine. Above, it is usually distinct, but inferiorly it is poorly defined and frequently absent. The anterior gluteal line, the longest, begins near the midpoint of the superior margin of the greater sciatic notch and ascends forwards into the outer lip of the crest, a little anterior to its tubercle. The inferior gluteal line, seldom well marked, begins posterosuperior to the anterior inferior iliac spine, curving posteroinferiorly to end near the apex of the greater sciatic notch. Between the inferior gluteal line and the acetabular margin is a rough, shallow groove. Behind the acetabulum, the lower gluteal surface is continuous with the posterior ischial surface, the conjunction marked by a low elevation.
The articular capsule is attached to an area adjoining the acetabular margin, most of which is covered by gluteus minimus. Posteroinferiorly, near the union of the ilium and ischium, the bone is related to piriformis.
The iliac fossa, the internal concavity of the ilium, faces anterosuperiorly. It is limited above by the iliac crest, in front by the anterior border and behind by the medial border, separating it from the sacropelvic surface. It forms the smooth and gently concave posterolateral wall of the greater pelvis. Below it is continuous with a wide shallow groove, bounded laterally by the anterior inferior iliac spine and medially by the iliopubic ramus.
The converging fibres of iliacus occupy the wide groove between the anterior inferior iliac spine and the iliopubic ramus laterally and the tendon of psoas major medially; the tendon is separated from the underlying bone by a bursa. The right iliac fossa contains the caecum, and often the vermiform appendix and terminal ileum. The left iliac fossa houses the terminal part of the descending colon and the proximal sigmoid colon.
The sacropelvic surface, the posteroinferior part of the medial iliac surface, is bounded posteroinferiorly by the posterior border, anterosuperiorly by the medial border, posterosuperiorly by the iliac crest and anteroinferiorly by the line of fusion of the ilium and ischium. It is divided into iliac tuberosity and auricular and pelvic surfaces. The iliac tuberosity, a large, rough area below the dorsal segment of the iliac crest, shows cranial and caudal areas separated by an oblique ridge and connected to the sacrum by the interosseous sacroiliac ligament. The sacropelvic surface gives attachment to the posterior sacroiliac ligaments and, behind the auricular surface, to the interosseous sacroiliac ligament. The iliolumbar ligament is attached to its anterior part. The auricular surface, immediately anteroinferior to the tuberosity, articulates with the lateral sacral mass. Shaped like an ear, its widest part is anterosuperior, and its ‘lobule’ posteroinferior and on the medial aspect of the posterior inferior spine. Its edges are well defined but the surface, though articular, is rough and irregular. It articulates with the sacrum and is reciprocally shaped. The anterior sacroiliac ligament is attached to its sharp anterior and inferior borders. The narrow part of the pelvic surface, between the auricular surface and the upper rim of the greater sciatic notch, often shows a rough pre-auricular sulcus (that is usually better defined in females) for the lower fibres of the anterior sacroiliac ligament. For the reliability of this feature as a sex discriminant, refer to and . The pelvic surface is anteroinferior to the acutely curved part of the auricular surface, and contributes to the lateral wall of the lesser pelvis. Its upper part, facing down, is between the auricular surface and the upper limb of the greater sciatic notch; the lower part faces medially and is separated from the iliac fossa by the arcuate line. Anteroinferiorly, the pelvic surface extends to the line of union between the ilium and ischium.
The attachment of sartorius extends down the anterior border below the anterior superior iliac spine. The iliac crest gives attachment to the anterolateral and dorsal abdominal muscles, and to the fasciae and muscles of the lower limb. The fascia lata and iliotibial tract are attached to the outer lip and tubercle of its ventral segment. Tensor fasciae latae is attached anterior to the tubercle. The lower fibres of external oblique and, just behind the summit of the crest, the lowest fibres of latissimus dorsi are attached to its anterior two-thirds. A variable interval exists between the most posterior attachment of external oblique and the most anterior attachment of latissimus dorsi, and here the crest forms the base of the lumbar triangle through which herniation of abdominal contents may rarely occur. Internal oblique is attached to the intermediate area of the crest. Transversus abdominis is attached to the anterior two-thirds of the inner lip of the crest, and behind this to the thoracolumbar fascia and quadratus lumborum. The most superior fibres of gluteus maximus are attached to the dorsal segment of the crest on its lateral slope. Erector spinae arises from the medial slope of the dorsal segment. The straight head of rectus femoris is attached to the upper area of the anterior inferior spine. Some fibres of piriformis are attached in front of the posterior inferior spine on the upper border of the greater sciatic foramen.
The gluteal surface is divided by three gluteal lines into four areas. Behind the posterior line, the upper rough part gives attachment to the upper fibres of gluteus maximus and the lower, smooth region to part of the sacrotuberous ligament and iliac head of piriformis. Gluteus medius is attached between the posterior and anterior lines, below the iliac crest, and gluteus minimus is attached between the anterior and inferior lines. The fourth area, below the inferior line, contains vascular foramina.
The reflected head of rectus femoris attaches to a curved groove above the acetabulum. Iliacus is attached to the upper two-thirds of the iliac fossa and is related to its lower one-third. The medial part of quadratus lumborum is attached to the anterior part of the sacropelvic surface, above the iliolumbar ligament. Piriformis is sometimes partly attached lateral to the pre-auricular sulcus, and part of obturator internus is attached to the more extensive remainder of the pelvic surface.
Branches of the iliolumbar artery run between iliacus and the ilium; one or more enter large nutrient foramina lying posteroinferiorly in the iliac fossa. The superior gluteal, obturator and superficial circumflex iliac arteries contribute to the periosteal supply. The obturator artery may supply a nutrient branch. Vascular foramina on the ilium underlying the gluteal muscles may lead into large vascular canals in the bone.
The periosteum is innervated by branches of nerves that supply muscles attached to the bone, the hip joint and the sacroiliac joint.
Ossification of the ilium is described on page 1355 .
The ischium, the inferoposterior part of the hip bone, has a body and ramus. The body has upper and lower ends and femoral, posterior and pelvic surfaces (see Figs 77.4 – 77.5 ). Above, it forms the posteroinferior part of the acetabulum; below, its ramus ascends anteromedially at an acute angle to meet the inferior pubic ramus, thereby completing the boundary of the obturator foramen. The ischiofemoral ligament is attached to the lateral border below the acetabulum ( ).
The femoral surface faces downwards, forwards and laterally towards the thigh. It is bounded in front by the margin of the obturator foramen. The lateral border, indistinct above but well defined below, forms the lateral limit of the ischial tuberosity. At a higher level the femoral surface is covered by piriformis, from which it is partially separated by the sciatic nerve and the nerve to quadratus femoris. The posterior surface, facing superolaterally, is continuous above with the iliac gluteal surface, and here a low convexity follows the acetabular curvature. Inferiorly, this surface forms the upper part of the ischial tuberosity, above which is a wide, shallow groove on its lateral and medial aspects. Above the ischial tuberosity the posterior surface is crossed by the tendon of obturator internus and the gemelli. The nerve to quadratus femoris lies between these structures and the ischium. The ischial tuberosity is a large, rough area on the lower posterior surface and inferior extremity of the ischium. Though obscured by gluteus maximus in hip extension, it is more readily palpable in hip flexion. It is 5 cm from the midline and about the same distance above the gluteal fold. It is elongated and widest above, and tapers inferiorly. The posterior aspect of the ischium lies between its lateral and posterior borders. The posterior border blends above with that of the ilium, helping to complete the inferior rim of the greater sciatic foramen, the posterior end of which has a conspicuous ischial spine. Below this the rounded border forms the floor of the lesser sciatic foramen, between the ischial spine and tuberosity. The pelvic surface is smooth and faces the pelvic cavity; inferiorly, it forms part of the lateral wall of the ischio-anal fossa.
The ischial ramus has anteroinferior and posterior surfaces continuous with the corresponding surfaces of the inferior pubic ramus. The anteroinferior surface is roughened by the attachment of the medial thigh muscles. The smooth posterior surface is partly divided into perineal and pelvic areas, like the inferior pubic ramus. The upper border completes the obturator foramen; the rough lower border, together with the medial border of the inferior pubic ramus, contributes to the pubic arch. The fascia overlying the superficial muscles of the perineum is attached below the ridge between the perineal and pelvic areas of the posterior surface of the ischial ramus. Above the ridge, areas give attachment to the crus of the penis or clitoris and the external urethral sphincter. The lower border of the ramus provides an attachment for the fascia lata and the stratum membranosum perinei.
The ischial tuberosity is divided nearly transversely into upper and lower areas. The upper area is subdivided by an oblique line into superolateral and inferomedial parts. The lower area, narrowing as it curves on to the inferior ischial aspect, is subdivided by an irregular vertical ridge into lateral and medial areas. The medial area is covered by fibroadipose tissue that usually contains the sciatic bursa of gluteus maximus, which supports the body in sitting. Medially the tuberosity is limited by a curved ridge that passes on to the ramus and which gives attachment to the sacrotuberous ligament and its falciform process.
The ischial spine projects downwards and a little medially (see Fig. 77.4B ). The sacrospinous ligament is attached to its margins, separating the greater from the lesser sciatic foramen. The ligament is crossed posteriorly by the internal pudendal vessels, pudendal nerve and the nerve to obturator internus.
Part of obturator externus is attached to the lower femoral surface of the ischial body. Part of obturator externus, the anterior fibres of adductor magnus and, near the lower border, gracilis are all attached to the anterior surface of the ischial ramus. Between adductor magnus and gracilis, the attachment of adductor brevis may descend from the inferior pubic ramus. The posterior surface is divided into pelvic and perineal areas. The pelvic area, facing back, has part of obturator internus attached to it. The perineal area faces medially; its upper part is related to the crus of the penis or clitoris, and its lower part gives attachment to sphincter urethrae, ischiocavernosus and the superficial transverse perineal muscle.
The ischial tuberosity gives attachment to the posterior thigh muscles. Quadratus femoris is attached along the upper part of its lateral border. The upper area of the tuberosity is subdivided by an oblique line into a superolateral part for semimembranosus and an inferomedial part for the long head of biceps femoris and semitendinosus. The lower area is subdivided by an irregular vertical ridge into lateral and medial areas. The larger lateral area is for part of adductor magnus. Superomedial to the tuberosity, the posterior surface has a wide, shallow groove, usually covered by hyaline cartilage, with a bursa between it and the tendon of obturator internus. Gemellus inferior is attached to the lower margin of the groove, near the tuberosity. Gemellus superior is attached to the upper margin, near the ischial spine. Forceful activation and/or severe stretch of the hamstrings can result in an avulsion fracture of the ischial tuberosity.
The pelvic surface of the ischial spine gives attachment to coccygeus and to the most posterior fibres of levator ani. Obturator internus is attached to the upper part of the smooth pelvic ischial surface and converges on the bony part of the lesser sciatic foramen, covering the rest of this surface other than the pelvic aspect of the ischial spine; the muscle and its fascia separate the bone from the ischio-anal fossa.
There are multiple vascular foramina at the acetabular margins and a few are usually present on the pelvic surface. Branches of the obturator, medial circumflex femoral and inferior gluteal arteries supply the ischium.
The periosteum is innervated by branches of nerves that supply the hip joint and muscles attached to the bone.
Ossification of the ischium is described on page 1355 .
See Chapter 46 .
See Chapter 46 .
The term pelvis (‘basin’) is applied variously to the skeletal ring formed by the hip bones and the sacrum, the cavity therein and even the entire region where the trunk and lower limbs meet ( Fig. 77.8 ). It is used here in the skeletal sense, to describe the irregular osseous girdle between the femoral heads and fifth lumbar vertebra. It is large because its primary function is to withstand the forces of body weight and musculature. In this section, its obstetric, forensic and anthropological significance will be considered.
The pelvis can be regarded as having greater and lesser segments, the false and true pelves, respectively. The segments are arbitrarily divided by an oblique plane passing through the sacral promontory posteriorly and the lineae terminales elsewhere. Each linea terminalis includes the iliac arcuate line, pectineal line (pecten pubis) and pubic crest.
The greater pelvis consists of the ilium and pubis above the lineae terminales and the base of the sacrum. This junctional zone is structurally massive and forms powerful arches from the acetabular fossae to the vertebral column around the visceral cavity, which is part of the abdomen. It has little anterior wall because of the pelvic inclination.
The pelvic inlet or brim may be round or oval in shape, and is indented posteriorly by the sacral promontory. The pelvic brim is obstetrically important and has also long been measured for anthropological reasons, as has the pelvic cavity.
By convention, the pelvic inlet is described in three dimensions. The anteroposterior diameter (true conjugate) is measured between the midpoints of the sacral promontory and upper border of the pubic symphysis, and on average is 10 cm in the adult male and 11.2 cm in the adult female. The transverse diameter is the maximum distance between similar points (assessed by eye) on opposite sides of the pelvic brim, and is on average 12.5 cm in the adult male and 13.1 cm in the adult female. The oblique diameter is measured from the iliopubic ramus to the opposite sacroiliac joint, and is on average 12 cm in the adult male and 12.5 cm in the adult female. These measurements vary with the individual and with racial group. In children, dimensions of the thorax and spine are significantly correlated with the width of the pelvic inlet, which are age-independent predictors of paediatric chest width and may be useful in assessing growth of the thorax and spine in children with early-onset spinal deformity ( ).
The lesser pelvis encloses a true basin when soft tissues of the pelvic floor are in place. Skeletally, it is a narrower continuation of the greater pelvis, with irregular but more complete walls around its cavity. Of obstetric importance, it has a curved median axis, and superior and inferior openings. The superior opening is occupied by viscera. The pelvic floor, viscera and subjacent perineal sphincters close the inferior opening.
The cavity of the lesser pelvis is short, curved and markedly longer in its posterior wall. Anteroinferiorly, it is bounded by pubic bones, their rami and symphysis. Posteriorly, it is bounded by the concave anterior sacral surface and coccyx. Laterally, on each side its margins are the smooth quadrangular pelvic aspect of the fused ilium and ischium. The region so enclosed is the pelvic cavity proper, through which pass the rectum, urinary bladder and parts of the reproductive organs. The cavity in females must also permit passage of the fetus.
The pelvic cavity diameters are measured at approximately the mid-level. The anteroposterior diameter is measured between the midpoints of the third sacral segment and posterior surface of the pubic symphysis, and is about 10.5 cm in the adult male and 13 cm in the adult female. The transverse diameter is the widest transverse distance between the side walls of the cavity, and often the greatest transverse dimension in the whole cavity. It measures about 12 cm in the adult male and 12.5 cm in the adult female. The oblique diameter is the distance from the lowest point of one sacroiliac joint to the midpoint of the contralateral obturator membrane, and measures about 11 cm in the adult male and 13.1 cm in the adult female. All measurements vary with the individual and with racial group.
Less regular in outline than the pelvic inlet, the pelvic outlet is indented behind by the coccyx and sacrum, and bilaterally by the ischial tuberosities. Its perimeter thus consists of three wide arcs. Anteriorly is the pubic arch, between the converging ischiopubic rami. Posteriorly and laterally on both sides are the sciatic notches between the sacrum and ischial tuberosities. The sciatic notches are divided by the sacrotuberous and sacrospinous ligaments into greater and lesser sciatic foramina ( Fig. 77.9 ). FLOAT NOT FOUND
With ligaments included, the pelvic outlet is rhomboidal. Its anterior limbs are the ischiopubic rami (joined by the inferior pubic (arcuate) ligament) and its posterior margins are the sacrotuberous ligaments, with the coccyx in the midline. The outlet is thus not rigid in its posterior half, being limited by ligaments and the coccyx, all slightly yielding. Even with the sacrum taken as the posterior midline limit (more reliable for measurement), there is typically slight mobility at the sacroiliac joints. Note also that a plane of the pelvic outlet is merely conceptual. The anterior, ischiopubic part has a plane that is inclined down and back to a transverse line between the lower limits of the ischial tuberosities, and the posterior half has a plane approximating to the sacrotuberous ligaments, sloping down and forwards to the same line.
Three measurements are made for the pelvic outlet. The anteroposterior diameter is usually measured from the apex of the coccyx to the midpoint of the lower rim of the pubic symphysis. The lowest sacral point may also be used (on average: male 8 cm, female 12.5 cm). The transverse (bituberous) diameter is measured between the ischial tuberosities at the lower borders of their medial surfaces (on average: male 8.5 cm, female 11.8 cm). The oblique diameter extends from the midpoint of the sacrotuberous ligament on one side to the contralateral ischiopubic junction (on average: male 10 cm, female 11.8 cm). All measurements vary among individuals and racial groups.
Apart from these main measurements, by consensus the basis of pelvic osteometry, other planes and measurements are used in obstetric practice. The plane of greatest pelvic dimensions is an obstetric concept. It represents the most capacious pelvic level, between the pelvic brim and midlevel plane, and corresponds with the latter anteriorly at the middle part of the pubic symphysis and posteriorly at the level of the second and third sacral segments.
The plane of least dimensions is said to be at about mid-pelvic level. Its transverse diameter is between the apices of the ischial spines. This measurement is about 9.5 cm in an adult female and is just wide enough to allow passage of the biparietal diameter of a fetal head (about 9 cm). Not surprisingly, most difficult parturition occurs here.
The above measurements are sometimes made in clinical practice using radiographs or magnetic resonance imaging (MRI) pelvimetry. Precise measurement is not possible without radiological techniques, and even these do not consider the adjacent soft tissues.
The axis of the superior pelvic aperture traverses its centre at right-angles to its plane, directed down and backwards ( Fig. 77.10 ). When prolonged (projected), it passes through the umbilicus and mid-coccyx. An axis is similarly established for the inferior aperture: projected upwards, it impinges on the sacral promontory. Axes can likewise be constructed for any plane, and one for the whole cavity is a concatenation of an infinite series of such lines (see Fig. 77.10 ).
The fetal head, however, descends in the axis of the inlet as far as the level of the ischial spines; it is then directed forwards into the axis of the vagina at right-angles to that axis. The form of this pelvic axis and the disparity in depth between the anterior and posterior contours of the cavity are prime factors in the mechanism of fetal transit in the pelvic canal.
In the standing position, the pelvic canal curves obliquely backwards relative to the trunk and abdominal cavity. The whole pelvis is tilted forwards, the plane of the pelvic brim making an angle of 50–60° with the horizontal. The plane of the pelvic outlet is tilted to about 15°. Strictly, the pelvic outlet has two planes: an anterior passing backwards from the pubic symphysis and a posterior passing forwards from the coccyx, both descending to meet at the intertuberous line. In standing, the pelvic aspect of the pubic symphysis faces nearly as much upwards as backwards and the sacral concavity is directed anteroinferiorly. The front of the pubic symphysis and anterior superior iliac spines are in the same vertical plane. While sitting, body weight is transmitted through the inferomedial parts of the ischial tuberosities, with variable soft tissues intervening. The anterior superior iliac spines are in a vertical plane through the acetabular centres, and the whole pelvis is tilted back with the lumbosacral angle somewhat diminished at the sacral promontory.
The skeletal pelvis supports and protects the contained viscera but is primarily part of the lower limbs, affording wide attachment for muscles of the thigh, leg and trunk. It constitutes the major mechanism for transmitting the weight of the head, trunk and upper limbs to the lower limbs. It may be considered as two arches divided by a coronal transacetabular plane. The posterior arch, chiefly concerned in transmitting weight, consists of the upper three sacral vertebrae and strong pillars of bone from the sacroiliac joints to the acetabular fossae. The anterior arch, formed by the pubic bones and their superior rami, connects these lateral pillars as a tie beam to prevent separation; it also acts as a compression strut against medial femoral thrust. The sacrum, as the summit of the posterior arch, is loaded at the lumbosacral joint. Theoretically, this force has two components: one thrusting the sacrum downwards and backwards between the iliac bones, the other thrusting its upper end downwards and forwards. Sacroiliac joint movements are regulated by osseous shape and massive ligaments. The first component therefore acts against the wedge, its tendency to separate iliac bones resisted by the sacroiliac and iliolumbar ligaments and pubic symphysis.
Vertical coronal sections through the sacroiliac joints suggest division of the (synovial) articular region of the sacrum into three segments. In the anterosuperior segment, involving the first sacral vertebra, the articular surfaces are slightly sinuous and almost parallel. In the middle segment, the posterior width between the articular markings is greater than the anterior, and centrally a sacral concavity fits a corresponding iliac convexity, an interlocking mechanism relieving the strain on the ligaments produced by body weight. In the posteroinferior segment, the anterior sacral width is greater than the posterior and here its sacral surfaces are slightly concave. Anteroinferior sacral dislocation by the second component (of force) is prevented, therefore, mainly by the middle segment, owing to its cuneiform shape and interlocking mechanism. However, some rotation occurs, in which the anterosuperior segment tilts down and the posteroinferior segment up. ‘Superior’ segmental movement is limited to a small degree by wedging but primarily by tension in the sacrotuberous and sacrospinous ligaments. In all movements, the sacroiliac and iliolumbar ligaments and pubic symphysis resist separation of the iliac bones.
The pelvis provides the most marked skeletal differences between male and female. Although there is some skeletal sexual dimorphism in infancy and childhood, most researchers agree that this is minimal. There are methods that focus on the shape of the greater sciatic notch, but they are quite unreliable. Sexual differences in adults are divisible into metrical and non-metrical features; the range of most features overlaps between the sexes.
Differences are inevitably linked to function. Although the primary pelvic function in both sexes is locomotor, the pelvis, particularly the lesser pelvis, is adapted to parturition in females, and these changes variably affect the proportions and dimensions of the greater pelvis ( ). Since males are stereotypically more muscular and therefore more heavily built, overall pelvic dimensions, such as the intercristal distance (distance between the iliac crests), are greater, markings for muscles and ligaments more pronounced, and general architecture more robust. The male iliac crest is more rugged and more medially inclined at its anterior end; in females the iliac crests are less curved in all parts. The iliac alae are more vertical in females but do not ascend so far; the iliac fossae are therefore shallower. These iliac peculiarities probably account for the greater prominence of female hips.
The male is more robust above the pelvis, with consequent differences at the lumbosacral and hip joints. The sacral basal articular facet for the fifth lumbar vertebra and intervening intervertebral disc is more than one-third of the total sacral basal width in males but less than one-third in females, in whom the sacrum is also relatively broader, accentuating this difference. The female has relatively broader sacral alae. The male acetabulum is larger, and its diameter is approximately equal to the distance between its anterior rim and pubic symphysis. In females, acetabular diameter is usually less than this distance, not only because it is smaller but also because the anterolateral wall of the cavity is comparatively and often absolutely wider. The height of the female pubic symphysis and adjoining parts of the pubis and ischium, which form the anterior pelvic wall, are also less, producing a somewhat triangular obturator foramen, which is more ovoid in males. Differing pubic growth is also expressed in the pubic arch below the pubic symphysis and between the inferior pubic rami. It is more angular in males, being 50–60°; in females it is rounded, less easy to measure and usually 80–85°. A greater separation of the pubic tubercles in females contributes to the pubic width. The ischiopubic rami are also much more lightly built and narrowed near the symphysis; in males they bear a distinctly rough, everted area for attachment of the penile crura and in females the corresponding attachment for the clitoris is the ventral arc. The ischial spines are closer in males and are more inturned. The greater sciatic notch is usually wider in females: mean values for males and females are 50.4° and 74.4°, respectively. The greater female values for angle and width are associated with increased backward sacral tilt and greater anteroposterior pelvic diameter, especially at lower levels.
The sacrum also displays metrical sexual differences. Female sacra are less curved, the curvature being most marked between the first and second segments and the third and fifth, with an intervening flatter region. Male sacra are more evenly curved, and relatively long and narrow, and more often exceed five segments (by addition of a lumbar or coccygeal vertebra). The sacral index compares sacral breadth (between the most anterior points on the auricular surfaces) with length (between midpoints on the anterior margins of the promontory and apex): average values for males and females are 105% and 115%, respectively. Auricular surfaces are relatively smaller and more oblique in females, but extend on to the upper three sacral vertebrae in both sexes. The dorsal auricular border is more concave in females. Many differences may be summarized in the generalization that the pelvic cavity is longer and more conical in males, and shorter and more cylindrical in females; the axis is curved in both. Differences are greater at the inferior aperture than at the brim, where in absolute measurements males are not as different from females as sometimes stated.
In forensic practice, identification of human skeletal remains (which are sometimes fragmentary) usually involves estimation of sex, and this is most reliably established from an examination of the pelvis. Even fragments of the pelvis can be useful in this respect, and may be considered alongside skull robusticity or gracility and long bone metrics. Pelvic features taken into account include the subpubic angle, pubic width, sacral curvature, width of the greater sciatic notch, and the proportion of the body of the first sacral vertebra compared to the alae. It is important to consider all data available for measuring skeletal sexual dimorphism of the pelvis and skull, as assessment of sex from isolated and often incomplete human remains is less reliable. For further details, consult .
The femur is the longest and strongest bone in the human body ( Figs 77.11 – 77.12 ). Its length is associated with a striding gait, and its strength with the weight and muscular forces it is required to withstand. Its shaft, almost cylindrical along most of its length, is bowed forwards. It has a proximal rounded, articular head projecting medially from its short neck, which, in turn, is a medial extension of the proximal shaft. The distal extremity is wider and more substantial, and presents two condyles that articulate with the tibia. In standing, the femoral shafts show an inclination upwards and outwards from their tibial articulations, with the femoral heads being separated by the pelvic width. Since the tibia and fibula descend vertically from the knees, the ankles are also in the line of body weight in standing or walking. The degree of femoral obliquity varies between individuals but is generally greater in women, reflecting the relatively greater pelvic breadth and shorter femora. Proximally, the femur consists of a head, neck and greater and lesser trochanters.
The femoral head faces anterosuperomedially to articulate with the acetabulum ( Fig. 77.13 ). The head, often described as rather more than half a ‘sphere’, is not part of a true sphere but is spheroidal. Its smoothness is interrupted posteroinferior to its centre by a small, rough fovea, to which the ligament of the head of the femur (ligamentum teres) is attached. The head is intracapsular and is encircled, distal to its equator, by the acetabular labrum. Its articular margin is distinct, except anteriorly, where the articular surface extends on to the neck. The anterior surface of the head is separated inferomedially from the femoral artery by the tendon of psoas major, the iliopectineal bursa and the articular capsule.
The femoral neck (see Fig. 77.13 ) is approximately 5 cm long, narrowest in its mid part and widest laterally, and connects the head to the shaft at an average angle of approximately 127° ( ) (angle of inclination; neck–shaft angle). The neck is also anteriorly rotated with respect to the shaft (angle of anteversion) some 10–15°, although values of this angle vary between individuals and between populations ( ). The contours of the neck are rounded; the upper surface is almost horizontal and slightly concave, while the lower is straighter but oblique, directed inferolaterally and backwards to the shaft near the lesser trochanter. On all aspects the neck expands as it approaches the articular surface of the head. Morphological variation of this bony expansion may cause painful impingement between the femoral neck and acetabular labrum at the extremes of flexion and medial (internal) rotation positions. The anterior surface of the neck is flat and marked at the junction with the shaft by a rough intertrochanteric line. The posterior surface, facing posteriorly and superiorly, is transversely convex, and concave in its long axis; its junction with the shaft is marked by a rounded intertrochanteric crest. There are numerous vascular foramina, especially anteriorly and posterosuperiorly.
The anterior surface is intracapsular, the capsule attaching laterally to the intertrochanteric line. Facets, often covered by extensions of articular cartilage, and various imprints frequently occur here. On the posterior surface the capsule does not reach the intertrochanteric crest; little more than the medial half of the neck is intracapsular. The anterior surface adjoining the head and covered by cartilage is related to the iliofemoral ligament. A groove, produced by the tendon of obturator externus as it approaches the trochanteric fossa, spirals across the posterior surface of the neck of the femur in a proximolateral direction.
The greater trochanter is large and quadrangular, projecting up from the junction of the neck and shaft (see Fig. 77.13 ). The leverage of many hip muscles is enhanced by their attachment to this prominent bony feature. Its posterosuperior region projects superomedially to overhang the adjacent posterior surface of the neck and here its medial surface presents the rough trochanteric fossa. The proximal border of the trochanter lies approximately a hand’s breadth below the iliac tuberculum, level with the centre of the femoral head. It has an anterior rough impression. Its lateral surface, continuous distally with the lateral surface of the femoral shaft, is crossed anteroinferiorly by an oblique, flat strip, which is wider above. This surface is readily palpable, especially when the muscles are relaxed.
The lesser trochanter is a conical posteromedial projection of the shaft at the posteroinferior aspect of its junction with the neck. Its summit and anterior surface are rough, but its posterior surface, at the distal end of the intertrochanteric crest, is smooth. It is not palpable. The lesser trochanter serves as the primary attachment for the large iliopsoas muscle.
The intertrochanteric line, a prominent ridge at the junction of the anterior surfaces of the neck and shaft, descends medially from a tubercle on the upper part of the anterior aspect of the greater trochanter to a point on the lower border of the neck, anterior to the lesser trochanter, where there may also be a tubercle. This line is the lateral limit of the hip joint capsule anteriorly. The upper and lower bands of the iliofemoral ligament are attached to its proximal and distal ends and the associated tubercles. Distally, it is continuous with the spiral (pectineal) line.
The intertrochanteric crest, a smooth and prominent ridge at the junction of the posterior surface of the neck with the shaft, descends medially from the posterosuperior angle of the greater trochanter to the lesser trochanter. A little above its centre is the low, rounded quadrate tubercle. It is covered by gluteus maximus, from which it is separated, medial to the tubercle, by quadratus femoris and the upper border of adductor magnus.
The gluteal tuberosity, accepting the tendon of the gluteus maximus, may be an elongated depression or a ridge. It may at times be prominent enough to merit the title of a third trochanter.
The shaft is surrounded by muscles and is impalpable (see Figs 77.11B , 77.12B ). The distal anterior surface, for 5–6 cm above the patellar articular surface, is covered by a suprapatellar bursa, between bone and muscle. The proximal two-thirds of the anterior and lateral surfaces are covered by vastus intermedius. The medial surface, devoid of attachments, is covered by vastus medialis.
The shaft is narrowest centrally, expanding a little at its proximal end, and substantially more at its distal end. Its long axis makes an angle of approximately 10° with the vertical, and diverges 5–7° from the long axis of the tibia. Its middle one-third has three surfaces and borders. The extensive anterior surface, smooth and gently convex, is between the lateral and medial borders, which are both round and indistinct. The posterolateral surface is bounded posteriorly by the broad, rough and often raised, linea aspera, usually a crest with lateral and medial edges. Its subjacent compact bone is augmented to withstand compressive forces, which are concentrated here by the anterior curvature of the shaft. The linea aspera gives at least partial attachment to adductors longus and brevis, adductor magnus, vastus medialis and lateralis, intermuscular septa (partially continuous with the fascia lata of the thigh), and the short head of biceps femoris, all inseparably blended at their attachments. Perforating arteries cross the linea aspera laterally under tendinous arches in adductor magnus and biceps femoris. Nutrient foramina, directed proximally, appear in the linea aspera, varying in number and site, one usually near its proximal end, a second usually near its distal end. The posteromedial surface, smooth like the others, is bounded in front by the indistinct medial border and behind by the linea aspera. In its proximal third the shaft has a fourth, posterior surface, bounded medially by the narrow, rough spiral line. Laterally, this surface is limited by the broad, rough gluteal tuberosity, ascending a little laterally to the greater trochanter and descending to the lateral edge of the linea aspera. In its distal one-third, the posterior surface of the shaft presents a further surface, the popliteal surface (see below) between the medial and lateral supracondylar lines. These lines are continuous above with the corresponding edges of the linea aspera. The lateral line is most distinct in its proximal two-thirds, where the short head of biceps femoris and lateral intermuscular septum are attached. Its distal third has a small, rough area for the attachment of plantaris, often encroaching on the popliteal surface. The medial line is indistinct in its proximal two-thirds, where vastus medialis is attached. Distally, the femoral vessels entering the popliteal fossa from the adductor canal cross the medial line obliquely. Further distally, the line is often sharp for 3 or 4 cm proximal to the adductor tubercle.
The popliteal surface, triangular in outline, lies between the medial and lateral supracondylar lines. In its distal medial part, it is rough and slightly elevated. Forming the proximal part of the floor of the popliteal fossa, the popliteal surface is covered by a variable amount of fat that separates the popliteal artery from bone. The superior medial genicular artery, a branch of the popliteal artery, arches medially above the medial condyle. It is separated from bone by the medial head of gastrocnemius. The latter is attached a little above the condyle; further distally, there may be a smooth facet underlying a bursa for the medial head of gastrocnemius. More medially, there is often an imprint proximal to the articular surface; in deep flexion, this is close to a rough tubercle on the medial tibial condyle for the attachment of semimembranosus. The superior lateral genicular artery arches up laterally proximal to the lateral condyle but is separated from bone by the attachment of plantaris to the distal part of the lateral supracondylar line.
The distal end of the femur is widely expanded as a bearing surface for transmission of weight to the tibia ( Fig. 77.14 ). It bears two massive condyles, which are partly articular. Anteriorly, the condyles are confluent and continue into the shaft; posteriorly, they are separated by a deep intercondylar fossa and project beyond the plane of the popliteal surface. The articular surface is a broad area, like an inverted U, for the patella and the tibia. The patellar surface extends anteriorly on both condyles, especially the lateral. It is transversely concave, vertically convex and grooved for the posterior patellar surface. The tibial surface is divided by the intercondylar fossa but is anteriorly continuous with the patellar surface. Its medial part is a broad strip on the convex inferoposterior surface of the medial condyle, and is gently curved with a medial convexity. Its lateral part covers similar aspects of the lateral condyle but is broader and passes straight back. The tibial surfaces are convex in all directions. The medial and lateral tibial surfaces have dissimilar anteroposterior curvatures; as evident in Fig. 77.14 , the medial condyle curves more obliquely than the lateral. As described in Chapter 78 on the knee, these differences are believed to be important determinants in the mechanics of locking the knee in full extension.
The patellar surface extends more proximally on the lateral side. Its proximal border is therefore oblique and runs distally and medially, separated from the tibial surfaces by two faint grooves that cross the condyles obliquely. The lateral groove is the more distinct. It runs laterally and slightly forwards from the front of the intercondylar fossa and expands to form a faint triangular depression, resting on the anterior edge of the lateral meniscus when the knee is fully extended. The medial groove is restricted to the medial part of the medial condyle and rests on the anterior edge of the medial meniscus in full extension. Where it ceases, the patellar surface continues back to the lateral part of the medial condyle as a semilunar area adjoining the anterior region of the intercondylar fossa. This area articulates with the medial vertical facet of the patella in full flexion; its outline is indistinct in most femora.
The intercondylar fossa separates the two condyles distally and behind. In front, the distal border of the patellar surface limits it, and behind an intercondylar line limits it, separating it from the popliteal surface. It is intracapsular but largely extrasynovial. Its lateral wall, the medial surface of the lateral condyle, bears a flat posterosuperior impression that spreads to the floor of the fossa near the intercondylar line for the proximal attachment of the anterior cruciate ligament. The medial wall of the fossa, i.e. the lateral surface of the medial condyle, bears a similar larger area, but far more anteriorly, for the proximal attachment of the posterior cruciate ligament. Both impressions are smooth and largely devoid of vascular foramina, whereas the rest of the fossa is rough and pitted by vascular foramina. A bursal recess between the ligaments may ascend to the fossa. The capsular ligament and, laterally, the oblique popliteal ligament are attached to the intercondylar line. The infrapatellar synovial fold is attached to the anterior border of the fossa.
The lateral condyle (see Fig. 77.14 ) is larger anteroposteriorly than the medial condyle. Its most prominent point is the lateral epicondyle to which the fibular collateral ligament is attached ( Fig. 77.15 ). A short groove, deeper in front, separates the lateral epicondyle inferiorly from the articular margin. This groove allows the tendon of popliteus to run deep to the fibular collateral ligament and insert inferior and anterior to the ligament insertion. Adjoining the joint margin is a strip of condyle, 1 cm broad. It is intracapsular and covered by synovial membrane except for the attachment of popliteus.
The medial surface is the lateral wall of the intercondylar fossa. Its lateral surface projects beyond the shaft. Part of the lateral head of gastrocnemius is attached to an impression posterosuperior to the lateral epicondyle.
The medial condyle has a bulging, convex medial aspect, which is easily palpable. Proximally, its adductor tubercle, which may only be a facet rather than a projection, receives the tendon of adductor magnus. The medial prominence of the condyle, the medial epicondyle, is anteroinferior to the tubercle. The lateral surface of the condyle is the medial wall of the intercondylar fossa. The condyle projects distally so that, despite the obliquity of the shaft, the profile of the distal end is almost horizontal. A curved strip, 1 cm wide and adjoining the medial articular margin, is covered by synovial membrane and is inside the joint capsule. Proximal to this, the medial epicondyle receives the tibial collateral ligament.
The femoral shaft is a cylinder of compact bone with a large medullary cavity. The wall is thick in its middle third, where the femur is narrowest and the medullary cavity most capacious. Proximally and distally the compact wall becomes progressively thinner, and the cavity gradually fills with trabecular bone. The extremities, especially the articular areas, consist of trabecular bone within a thin shell of compact bone, their trabeculae being disposed along lines of greatest stress. At the proximal end the main trabeculae form a series of plates orthogonal to the articular surface, converging to a central dense wedge, which is supported by strong trabeculae passing to the sides of the neck, especially along its upper and lower profiles ( Fig. 77.16 ). Force applied to the femoral head is therefore transmitted to the wedge and from there to the junction of the neck and shaft. This junction is strengthened by dense trabeculae extending laterally from the lesser trochanter to the end of the superior aspect of the neck, thus resisting tensile or shearing forces applied to the neck through the head ( Fig. 77.17 ). Tensile and compressive tests indicate that axial trabeculae of the femoral head withstand much greater stresses than peripheral trabeculae. A smaller bar across the junction of the greater trochanter with the neck and shaft resists shearing caused by forces produced by local muscles such as the gluteus medius. A thin vertical plate, the so-called calcar femorale, ascends from the compact wall near the linea aspera into the trabeculae of the neck (see Fig. 77.17 ). Medially, it joins the posterior wall of the neck; laterally, it continues into the greater trochanter, where it disperses into general trabecular bone. It is thus in a plane anterior to the trochanteric crest and base of the lesser trochanter. demonstrated that the trabecular framework of the proximal femur was spiral, and that the ‘arches’ were simplified sectional profiles of this spiral. At the distal end of the femur, trabeculae spring from the entire internal surface of compact bone, descending perpendicular to the articular surface. Proximal to the condyles these are strongest and most accurately perpendicular. Horizontal planes of trabecular bone, arranged like crossed girders, form a series of cubical compartments.
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The greater trochanter provides attachment for glutei medius and minimus. Gluteus minimus is attached to its rough anterior impression and gluteus medius to its posterosuperior aspect and an oblique line on its lateral surface. The bone is separated from the tendons of gluteus minimus and medius by several bursae ( ). The area behind it is covered by deep fibres of gluteus maximus, with part of its trochanteric bursa interposed. The tendon of piriformis is attached to the upper border of the trochanter and the common (tricipital) tendon of obturator internus and the gemelli is attached to its medial surface. The trochanteric fossa receives the tendon of obturator externus. Psoas major is attached to the summit and anteromedial surface of the lesser trochanter, and iliacus to the medial or anterior surface of its base, descending a little behind the spiral line as its tendon fuses with that of psoas major. Adductor magnus (upper part) passes over the posterior surface of the lesser trochanter, sometimes separated by an interposed bursa.
The most proximal fibres of vastus lateralis are attached to the proximal end of the intertrochanteric line, and those of vastus medialis to the distal end. Quadratus femoris is attached to the quadrate tubercle and the immediately distal bone. Vastus intermedius is attached to the anterior and lateral surfaces of the proximal three-quarters of the femoral shaft. Slips of articularis genus are attached distal to this.
The gluteal tuberosity receives the deeper fibres of the distal half of gluteus maximus and, at its medial edge, the uppermost fibres of adductor magnus. Distal to this, adductor magnus is attached to the linea aspera and, by an aponeurosis, to the proximal part of the medial supracondylar ridge. Its remaining fibres form a large tendon attached to the adductor tubercle, with an aponeurotic expansion to the distal part of the medial supracondylar ridge.
Pectineus and adductor brevis are attached to the posterior femoral surface between the gluteal tuberosity and spiral line. The pectineal attachment is a line, sometimes slightly rough, from the base of the lesser trochanter to the linea aspera. Adductor brevis is attached lateral to pectineus and beyond this to the proximal part of the linea aspera, medial to adductor magnus. Adductor longus, intermuscular septa and the short head of biceps femoris are also attached to the linea aspera. Vastus lateralis has a linear attachment from the anterior surface of the base of the greater trochanter to the proximal end of the gluteal tuberosity, and along the lateral margin of the latter to the proximal half of the lateral edge of the linea aspera. Vastus medialis is attached from the distal end of the intertrochanteric line along the spiral line to the medial edge of the linea aspera and thence to the medial supracondylar line, which also receives many fibres from the aponeurotic attachments of adductor magnus.
The medial head of gastrocnemius is attached to the posterior surface a little above the medial condyle. The short head of biceps femoris is attached to the proximal two-thirds of the lateral supracondylar line. Plantaris attaches to the line distally. Vastus medialis is attached to the proximal two-thirds of the medial supracondylar line.
Part of the lateral head of gastrocnemius is attached posterosuperiorly to the lateral epicondyle. Popliteus is attached anteriorly in the groove on the outer aspect of the lateral epicondyle. Its tendon passes deep to the fibular collateral ligament (see Fig. 77.15 ). The tendon lies in the groove in full knee flexion; in extension it crosses the articular margin and may form an impression on it.
The blood supply of the femoral head is derived from an arterial ring around the neck, just outside the attachment of the fibrous capsule, constituted by the medial and lateral circumflex femoral arteries with minor contributions from the superior and inferior gluteal vessels. Branches from the arterial ring pierce the capsule (under its zona orbicularis) to ascend the neck beneath the reflected synovial membrane. These vessels become the retinacular arteries and form a subsynovial intracapsular anastomosis. Here the vessels are at risk with a displaced fracture of the femoral neck. Interruption of blood supply in this way can lead to avascular necrosis of the femoral head. If the fracture is intracapsular, not only is the intraosseous blood supply damaged but the retinacular vessels are also vulnerable. If the fracture is extracapsular, the retinacular vessels will remain intact and avascular necrosis of the femoral head is much less likely. The ascending cervical vessels give off metaphysial branches that enter the neck, while the intracapsular ring gives off lateral and inferior epiphysial branches. A small medial epiphysial supply reaches the head along the ligament of the head of femur by the acetabular branches of the obturator and medial circumflex femoral arteries, which anastomose with the other epiphysial vessels ( ). During growth, the epiphysial plate separates the territories of the metaphysial and epiphysial vessels; these vessels anastomose freely after osseous union of the head and neck. Observations of developmental patterns of this supply in late fetal and early postnatal periods have revealed that although the medial and lateral circumflex femoral arteries at first contribute equally, two major branches of the medial provide the final supply, both posterior to the neck. The supply from the lateral circumflex femoral artery diminishes and the arterial ring is interrupted. As the femoral neck elongates, the extracapsular circle becomes more distant from the epiphysial part of the head.
The trochanteric regions and subtrochanteric shaft are supplied by the trochanteric and cruciate arterial anastomoses. More distally in the shaft, nutrient foramina, directed proximally, are found in the linea aspera, varying in number and site: one is usually near its proximal end and a second usually near its distal end. The main nutrient artery is usually derived from the second perforating artery (see p. 1389 ). If two nutrient arteries occur, they may branch from the first and third perforators. Periosteal vessels arise from the perforators and from the profunda femoris artery, and run circumferentially rather than longitudinally. The distal metaphysis has many vascular foramina. Arterial supply here is from the genicular anastomosis. For further details, consult , .
In general, the pattern of venous drainage of the head and neck corresponds to that of the arteries, though there may be a single large cervical vein posteroinferiorly.
The periosteal innervation is derived proximally from nerves that supply the hip joint, distally from those supplying the knee, and in all areas from nerves that innervate muscles attached to the bone.
The femur ossifies from five centres: in the shaft, head, greater and lesser trochanters and the distal end ( Figs 77.18 – 77.19 ). Other than the clavicle, it is the first long bone to ossify.The process starts in the mid-shaft during embryonic stages 22 and 23 (postfertilization days 52–58) and extends to produce a miniature shaft that is largely ossified at birth. Secondary centres appear in the distal end (from which the condyles and epicondyles are formed) during postmenstrual weeks 33–36; in the greater trochanter during the fourth year; and in the lesser trochanter between the twelfth and fourteenth years. In the infant, the femoral head is entirely cartilaginous: it cannot be seen on plain radiographs and is best visualized using ultrasound ( Fig. 77.20 ). The centre in the cartilaginous head is restricted to it until the tenth year, so that the epiphysial line (see Fig. 77.7 ) is horizontal and the inferomedial part of the articular surface is on the neck. The medial epiphysial margin later grows over this part of the articular surface. Thus, the mature epiphysis is a hollow cup on the summit of the neck. The epiphysial line follows the articular margin except where it is separated superiorly from the articular surface by a non-articular area where blood vessels enter the head ( ). The epiphyses fuse independently: the lesser trochanter soon after puberty, followed by the greater trochanter. The capital epiphysis fuses in the fourteenth year in females and seventeenth year in males. The epiphysis at the distal end fuses in the sixteenth year in females, and eighteenth year in males. The distal epiphysial plate traverses the adductor tubercle.
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Trauma to any epiphysial plate can lead to bony union between epiphysis and metaphysis, and so cause premature cessation of growth. Any surgery in the hip region in children can injure the growth plate, resulting in abnormal proximal femoral development. In the case of fractures involving the epiphysis, expeditious restoration of normal bony alignment is essential in order to minimize the risk of subsequent abnormal growth.
The growth plate represents a line of weakness and predisposes to fracture from injury. Such acute injuries affecting the capital epiphysis are uncommon. However, a more chronic fracture through the capital epiphysis occurs in slipped capital femoral epiphysis (see Fig. 77.29 ). The condition affects pubescent adolescents, especially males. The femoral head epiphysis displaces posteriorly off the femoral neck. If it heals in this position, lower limb deformity and restricted hip movement occur. A classic hallmark is obligatory lateral (external) rotation of the femur as the hip is flexed. Treatment varies according to the time taken for the ‘slip’ to occur. Normal anatomical restoration is not attempted because of an increased incidence of avascular necrosis. The position of the femoral head may be accepted as it is and fixed with screws in this position to stop further displacement. This treatment will deliberately cause premature growth plate fusion and so prevent future ‘slippage’. Since the distal femoral growth plate accounts for most of the normal increase in longitudinal growth of the femoral shaft, an acceptable limb length difference usually results.
Infection of bone in neonates and young children tends to arise via bacteria in the blood stream that usually ‘seed’ in the metaphysial region, probably as a consequence of the vascular ‘arcade’ arrangement of arteries in this part of the bone. The proximal femoral growth plate is intra-articular. As a result, infection in the proximal femoral metaphysis can spread into the joint and result in a septic arthritis that can destroy the hip joint permanently.
The distal end of the femur is the only epiphysis in which ossification consistently starts just before birth; the phenomenon therefore serves as a reliable indicator of the gestational maturity of a stillborn baby. Since the epiphysial plate is level with the adductor tubercle, the epiphysis is partly extra-articular. Operations here may damage the distal epiphysial cartilage in children and result in subsequent shortening of the leg.
The pubic bones meet in the midline at the pubic symphysis, a secondary cartilaginous joint (see Figs 77.2 – 77.3 ).
The articulating surfaces are the medial (symphysial) surfaces of the pubic bones, each covered by a thin layer of tightly adherent hyaline cartilage (surface growth cartilage in the young). The junction is not flat but is marked by reciprocal crests and papillae. Theoretically, this would resist shearing. The surfaces of hyaline cartilage are connected by fibrocartilage, varying in thickness and constituting the interpubic disc. The interpubic disc often contains a cleft, which rarely appears before the tenth year and may have a synovial lining ( ). The cleft, which is larger and more prevalent in females, is usually posterosuperior but may extend the length and/or depth of the disc.
The interpubic disc is strengthened anteriorly by several interlacing collagenous fibrous layers, passing obliquely from bone to bone, decussating with fibres of the external oblique aponeuroses and the medial tendons of the recti abdominis. These layers constitute the anterior pubic ligament. There are less well developed posterior fibres, sometimes named the posterior pubic ligament. The main ligaments of the joint are the superior and inferior pubic ligaments. The superior pubic ligament connects the bones above, extending to the pubic tubercles. The inferior pubic ligament, a thick arch of fibres, connects the lower borders of the symphysial pubic surfaces bounding the pubic arch. It blends superiorly with the interpubic disc and extends laterally to the inferior pubic rami. Its inferior edge is separated from the anterior border of the perineal membrane by an opening, which is traversed by the deep dorsal vein of the penis or clitoris.
The pubic symphysis is supplied by pubic branches of the obturator, superficial external pudendal and inferior epigastric arteries.
The pubic symphysis is innervated by branches from the iliohypogastric, ilioinguinal and pudendal nerves.
The interpubic disc and the superior and inferior ligaments are the main stabilizing factors of the pubic symphysis.
Angulation, rotation and displacement are possible but slight, and are likely during movement at the sacroiliac and hip joints. The movements at the pubic symphysis range between 0.1 and 2 mm and are greater in the vertical axis than along the sagittal and transverse axes ( ). Excessive movement may occur following an injury. Some separation occurs late in gestation and during childbirth; on occasion, this is considerable.
Anteriorly the pubic symphysis is related to subcutaneous tissue and skin. Because of the obliquity of the joint, the proximal ends of the penile or clitoral shafts lie anterior to the lower half of the joint. Inferiorly the urethra lies about 2.5 cm away in the male, and somewhat closer in the female, as it passes through the perineal membrane. Closer to the joint, the deep dorsal vein of the penis or clitoris passes between the inferior pubic ligament and the anterior border of the perineal membrane. Posteriorly the upper part of the joint is separated from the inferolateral surfaces of the urinary bladder by the retropubic fat pad. Inferiorly in the male the prostatic venous plexus separates the prostate from the lower part of the joint. The region is sometimes termed the retropubic space (of Retzius). These relationships explain why traumatic disruption of the anterior bony pelvis may be associated with serious urogenital injury.
The sacroiliac joint occurs between the sacral and iliac auricular surfaces and, in essence, is a stress-relieving joint ( , ) (see Fig. 77.8A ). The joint consists of syndesmotic and synovial parts. Fibrous adhesions and gradual obliteration occur in both sexes, earlier in males and after menopause in females. Radiological evidence of obliteration in normal subjects is occasionally seen before 50 years but is not uncommon thereafter; in old age, the joint may be completely fibrosed and occasionally even ossified.
The surfaces are nearly flat in infants, whereas in adults they are irregular, often markedly so, and sometimes undulant. The curvatures and irregularities, greater in males, are reciprocal; they restrict movements and contribute to the considerable strength of the joint in transmitting weight from the vertebral column to the lower limbs. The sacral surface is covered by hyaline cartilage, which is thicker anteriorly than posteriorly in adults. The thinner cartilage on the iliac surface is also hyaline in type, as confirmed by the presence of type II collagen.
The capsule is attached close to both articular margins.
The ligaments of the sacroiliac joint are the anterior, interosseous and posterior sacroiliac, iliolumbar, sacrotuberous and sacrospinous ligaments.
The anterior sacroiliac ligament (see Fig. 77.9A ), an anteroinferior capsular thickening, is particularly well developed near the arcuate line and the posterior inferior iliac spine, where it connects the third sacral segment to the lateral side of the pre-auricular sulcus. It is thin elsewhere.
The interosseous sacroiliac ligament is the major bond between the bones, filling the irregular space posterosuperior to the joint. The posterior sacroiliac ligament covers it superficially. Its deeper part has superior and inferior bands passing from depressions posterior to the sacral auricular surface to those on the iliac tuberosity. These bands are covered by, and blend with, a more superficial fibrous sheet connecting the posterosuperior margin of a rough area posterior to the sacral auricular surface to the corresponding margins of the iliac tuberosity. This sheet is often partially divided into superior and inferior parts, the former uniting the superior articular process and lateral crest on the first two sacral segments to the neighbouring ilium as a short posterior iliac ligament (see Fig. 46.70 ).
The posterior sacroiliac ligament (see Fig. 77.9B ) overlies the interosseous ligament: the dorsal rami of the sacral spinal nerves and vessels intervene. It consists of several weak fasciculi connecting the intermediate and lateral sacral crests to the posterior superior iliac spine and posterior end of the internal lip of the iliac crest. Inferior fibres, from the third and fourth sacral segments, ascend to the posterior superior iliac spine and posterior end of the internal lip of the iliac crest; they may form a separate long posterior sacroiliac ligament. This ligament is continuous laterally with part of the sacrotuberous ligament and medially with the posterior lamina of the thoracolumbar fascia.
See Chapter 46 .
The sacrotuberous ligament (see Figs. 77.9 , 46.70 ) is attached by its broad base to the posterior superior iliac spine, the posterior sacroiliac ligaments (with which it is partly blended), lateral sacral crest and the lateral margins of the lower sacrum and upper coccyx. Its oblique fibres descend laterally, converging to form a thick, narrow band that widens again below and is attached to the medial margin of the ischial tuberosity. It then spreads along the ischial ramus as the falciform process, whose concave edge blends with the fascial sheath of the internal pudendal vessels and pudendal nerve. The lowest fibres of gluteus maximus are attached to the posterior surface of the ligament; superficial fibres of the lower part of the ligament continue into the superficial fibres of the tendon of the long head of biceps femoris. The coccygeal branches of the inferior gluteal artery, the perforating cutaneous nerve and filaments of the coccygeal plexus pierce the ligament.
The thin, triangular sacrospinous ligament (see Fig. 77.9 ) extends from the ischial spine to the lateral margins of the sacrum and coccyx anterior to the sacrotuberous ligament, with which it blends in part. Its anterior surface is the coccygeus muscle, i.e. muscle and ligament are coextensive. The sacrospinous ligament is often regarded as a degenerate part of coccygeus.
The sacrotuberous and sacrospinous ligaments convert the sciatic notches into foramina (see Fig. 77.9 ).
The greater sciatic foramen is bounded anterosuperiorly by the greater sciatic notch, posteriorly by the sacrotuberous ligament and inferiorly by the sacrospinous ligament and ischial spine (see Fig. 77.9 ). It is partly filled by the emerging piriformis, above which the superior gluteal vessels and nerve leave the pelvis. Below it, the inferior gluteal vessels and nerve, internal pudendal vessels and pudendal nerve, sciatic and posterior femoral cutaneous nerves and the nerves to obturator internus and quadratus femoris all leave the pelvis.
The lesser sciatic foramen is bounded anteriorly by the ischial body, superiorly by its spine and sacrospinous ligament, and posteriorly by the sacrotuberous ligament (see Fig. 77.9A ). It transmits the tendon of obturator internus, the nerve to obturator internus, and the internal pudendal vessels and pudendal nerve.
The arterial supply of the sacroiliac joint is derived from the iliolumbar, superior gluteal and superior lateral sacral arteries, with corresponding venous drainage. Lymphatic drainage follows the arteries, reaching the iliac and lumbar nodes.
Nerve fibres ramify within the joint capsule and adjoining ligaments, but their source is uncertain. It is thought that the joint probably receives branches from the anterior and posterior rami of the first two sacral spinal nerves, and from the superior gluteal nerve, and that there may also be contributions from the obturator nerve and the lumbosacral trunk.
The sacroiliac joint has sometimes been implicated as the source of pain in the lower back and buttocks. Diagnosing sacroiliac joint-mediated pain is difficult because the presenting complaints are similar to those seen with other causes of back pain. Patients with sacroiliac joint-mediated pain rarely report pain above the level of L5; most localize their pain to the area around the posterior superior iliac spine.
The sacroiliac joint is one of the most stable joints in the body and supports the weight of the trunk. The reciprocal irregularity of the joint surfaces allows very little movement. The tendency of the sacrum to be forced downwards by the trunk is resisted by the extremely strong posterior ligaments, while the iliolumbar ligaments help to resist displacement of the fifth lumbar vertebra over the sacrum. The sacrotuberous and sacrospinous ligaments oppose upward tilting of the lower part of the sacrum when downward thrust is applied at its upper end.
Primary movement of the sacroiliac joint is minimal ( ). All muscles that cross the joint act on the lumbar spine or on the hip. Such movements as do occur are secondarily imposed on the joint as the pelvis moves. Data from living subjects are technically difficult to obtain, and those based on plain radiographs are unreliable. Studies using implanted tantalum spheres and biplanar radiography have shown mean rotational ranges of less than 2°. Even when there is recordable movement, the direction of movement is irregular. Biplanar radiography has also shown that the axes of movement of the sacroiliac joint during hip movement are oblique, and that the axes differ in flexion and extension.
During pregnancy, the pelvic joints and ligaments loosen under the influence of the hormone relaxin. Movements in the joints increase. Relaxation renders the sacroiliac locking mechanism less effective, permitting greater rotation and perhaps allowing alterations in pelvic diameters at childbirth, although the effect is probably small. The impaired locking mechanism diverts the strain of weight-bearing to the ligaments, with frequent sacroiliac strain after pregnancy.
The sacroiliac joints have many important anterior relations. The internal and external iliac veins join to form the common iliac veins immediately anteriorly, separating the joints from the bifurcations of the common iliac arteries and, more anteriorly, the ureters. The lumbosacral trunk and the obturator nerve cross the anterior aspect of the joint behind the vessels. Piriformis partly attaches to the anterior capsule, separating the joint from the upper part of the sacral plexus.
Accessory sacroiliac articulations are not uncommon. They develop behind the articular surface between the lateral sacral crest and posterior superior iliac spine and iliac tuberosity, and are acquired fibrocartilaginous joints resulting from the stresses of weight-bearing. They have a joint capsule, are saddle-shaped, and may be single, double, unilateral or bilateral ( ).
The hip joint is a synovial joint of ball-and-socket (multiaxial spheroidal) type between the head of the femur and the cup-shaped (cotyloid) acetabulum; its centre lies a little inferior to the middle one-third of the inguinal ligament ( Fig. 77.21 ). FLOAT NOT FOUND
The femoral head can be landmarked from the surface roughly 2–4 cm superior to an approximate midpoint of a line joining the superior margin of the greater trochanter to the pubic tubercle. The articular surfaces of the femoral head and the acetabulum are reciprocally curved but neither coextensive nor completely congruent (see Fig. 77.21 ; see Fig. 77.16 ). The close-packed position of the hip joint is one of full extension, with slight abduction and medial rotation (see also Table 5.4 ). This position winds up most of the joint’s capsular ligaments, which can provide an important element of articular stability. The femoral head is covered by articular cartilage, except over the fovea where the ligament of the head of the femur (ligamentum teres) is attached. Anteriorly, the cartilage extends laterally over a small area on the adjoining neck. Articular cartilage is, generally, thicker centrally than peripherally. Cartilage thickness is maximal anterosuperiorly in the acetabulum and anterolaterally on the femoral head, the two areas that correspond to the principal load-bearing areas within the joint. The acetabular articular surface, the lunate surface, is an incomplete ring, broadest anterosuperiorly where the pressure of body weight falls in the erect posture, and narrowest in its pubic region. It is deficient inferiorly opposite the acetabular notch. The lunate surface is covered by articular cartilage, which is thickest where the surface is broadest. The acetabular fossa, the central non-articular area in the floor of the acetabulum, is devoid of cartilage but contains fibroelastic fat largely covered by synovial membrane. The acetabular labrum, a fibrocartilaginous rim attached to the acetabular margin, serves to deepen the acetabulum and bridges the acetabular notch by attaching to the peripheral edge of the transverse acetabular ligament. The acetabular labrum is triangular in section, attached by its base to the acetabular margin and blending with adjacent articular cartilage; its acute free edge projects beyond the acetabular margin. The diameter of the acetabular cavity is constricted by the labral rim, which embraces the femoral head, thereby contributing to the stability of the articulation. The acetabular labrum increases the surface area for joint contact as well as sealing the joint, allowing optimal intra-articular distribution of synovial fluid ( , ). It thus facilitates nutrition of the articular cartilage and helps to reduce intra-articular friction ( , ). Nerve endings found within the labrum suggest this structure may be a source of proprioception or, when injured, of pain ( , ). A torn acetabular labrum can be detected using MRI, to identify the site and severity of the lesion ( Fig. 77.22 ).
Ventral divisions | Dorsal divisions | |
---|---|---|
Nerve to quadratus femoris and gemellus inferior | L4–S1 | |
Nerve to obturator internus and gemellus superior | L5–S2 | |
Nerve to piriformis | L4–S2 | |
Superior gluteal | L4–S1 | |
Inferior gluteal | L5–S2 | |
Posterior femoral cutaneous | S2, S3 | S1, S2 |
Tibial (sciatic) | L4–S3 | |
Common fibular (sciatic) | L4–S2 | |
Perforating cutaneous | S2, S3 | |
Pudendal | S2–S4 | |
Branches to levator ani, coccygeus and external anal sphincter | S4 |
FLOAT NOT FOUND
The shape of the bones of the hip normally limits large and potentially damaging contact stress on adjacent connective tissues, especially during the extremes of movement. Consider, for example, the normal shape of the femoral head and neck region. Similar to the shape of a light bulb, the spherical femoral head narrows gradually at its junction with the neck of the femur. This tapering limits large contact stress between the femoral neck and the margin of the acetabulum. However, tapering may be lost because of natural variation or underlying pathology, resulting in a specific deformity that has been referred to as a cam deformity because the head and neck of the femur, together, resemble a camshaft. Although often subtle, this deformity may be detected radiographically (see arrow in Fig. 77.23 ). In some patients with a cam deformity, extreme and repeated motions of the hip, typically involving combinations of flexion, medial rotation and adduction, can create damaging impingement between the hard and bulbous femoral neck and the softer acetabular labrum. The anterosuperior section of the labrum is particularly vulnerable to this type of injury, which is a painful and often motion-limiting condition referred to as femoro-acetabular impingement syndrome. The repeatedly traumatized section of the labrum can become enlarged, fragmented or torn. When the acetabular labrum is torn, a hip joint may become unstable as a consequence of the loss of the natural suction seal around the joint. In some advanced cases, the impingement trauma may create lesions at the chondrolabral junction, resulting in damage to the adjacent articular cartilage, potentially predisposing the hip joint to degenerative arthritis (osteoarthrosis) ( ). Treatment may involve arthroscopic repair of the acetabular labrum and cartilage, as well as reshaping the area of the femoral head and neck responsible for the impingement. FLOAT NOT FOUND
The fibrous capsule of the hip joint is strong and dense. It is attached superiorly to the acetabular margin 5–6 mm medial to the labral attachment, anteriorly to the outer labral aspect and, near the acetabular notch, to the transverse acetabular ligament and the adjacent rim of the obturator foramen. From its acetabular attachment, it extends laterally to surround the femoral head and neck, and is attached anteriorly to the intertrochanteric line, superiorly to the base of the femoral neck, posteriorly 1 cm superomedial to the intertrochanteric crest, and inferiorly to the femoral neck near the lesser trochanter (see Fig. 77.12B ). Anteriorly, many fibres ascend along the neck as longitudinal retinacula, containing blood vessels for both the femoral head and the neck. The capsule is thicker anterosuperiorly, where maximal stress occurs, particularly while standing with the hip extended. Posteroinferiorly, it is relatively thin and loosely attached. The capsule as a whole has two sets of fibres, circular and longitudinal. The circular fibres (zona orbicularis) are internal and form a collar round the femoral neck; although partly blended with the pubofemoral and ischiofemoral ligaments, these fibres are not directly attached to bone. Externally, longitudinal fibres are most numerous in the anterosuperior region, where they are reinforced by the iliofemoral ligament. The capsule is also strengthened inferiorly by the pubofemoral ligament, and posteriorly by the ischiofemoral ligament. Externally the capsule is rough, covered by muscles and tendons, and separated anteriorly from psoas major and iliacus by a bursa. The capsular attachment to the femur lies well distal to the growth plate of the femoral head both anteriorly and posteriorly, and so the upper femoral epiphysis is entirely intracapsular. The capsular attachment intersects the growth plate of the greater trochanter on the superior surface of the base of the neck.
Iliocapsularis (also called iliacus minor or iliotrochantericus) is a little-known but constant muscle that lies immediately deep to the tendon of iliopsoas and overlies the anterior hip capsule ( , ). Typically present as just a few strands of fibres, it originates from the anteromedial hip capsule and anteroinferior iliac spine, and is attached just distal to the lesser trochanter. Although the function of the muscle is uncertain, it may draw the capsule taut as a way of reducing its impingement during hip flexion. For reasons not understood, the size of the iliocapsularis has been shown to be larger in hips with radiological evidence of developmental hip dysplasia ( )
The joint capsule is surrounded by muscles ( Fig. 77.24 ). Anteriorly, lateral fibres of pectineus separate the capsule from the femoral vein. Lateral to this, the tendon of psoas major, with iliacus lateral to it, descends en route to the lesser trochanter, partly separated from the capsule by a bursa. The femoral artery is anterior to the tendon of psoas major, and the femoral nerve lies deep in a groove between the tendon and iliacus. More laterally the straight head of rectus femoris crosses the joint with a deep layer of the iliotibial tract, which blends with the capsule under the lateral border of the muscle. Superiorly the reflected head of rectus femoris contacts the capsule medially, while gluteus minimus covers it laterally, being either closely adherent or comingled ( ). Inferiorly, medial fibres of pectineus adjoin the capsule and, more posteriorly, obturator externus spirals obliquely to its posterior aspect. Posteroinferiorly the capsule is covered by the tendon of obturator externus, separating it from quadratus femoris and accompanied by an ascending branch of the medial circumflex femoral artery. Superior to this the tendon of obturator internus and the gemelli contact the joint capsule, separating it from the sciatic nerve. The nerve to quadratus femoris is deep to the obturator internus tendon and descends medially on the capsule. Superior to this the posterior surface of the joint is crossed by piriformis. FLOAT NOT FOUND
The ligaments of the hip joint are the iliofemoral, pubofemoral, ischiofemoral and transverse acetabular ligaments, and the ligament of the head of the femur ( Fig. 77.25 ). As the hip moves, the capsular ligaments wind and unwind, tightening around the hip, and affecting stability, excursion and joint capacity ( ). Joint capacity is maximal when the hip joint is held in a partially flexed and abducted position; a patient with an effusion in the hip joint is therefore most comfortable when the joint is held in this position.
The iliofemoral ligament is very strong and is shaped like an inverted Y, lying anteriorly and intimately blended with the capsule. Its apex is attached between the anterior inferior iliac spine and acetabular margin, its base to the intertrochanteric line. It is composed of a medially placed, thicker descending part and a laterally placed, transverse part, which is typically distinguishable anteriorly. The obliquely disposed transverse part is attached to a tubercle at the superolateral end of the intertrochanteric line, while the vertically oriented descending part reaches the inferomedial end of the line.
The pubofemoral ligament is triangular, with a base that is attached to the iliopubic ramus, superior pubic ramus, obturator crest and membrane. It blends distally with the capsule and deep surface of the descending part of the iliofemoral ligament and has been described as consisting of multiple crura ( ).
The ischiofemoral ligament thickens the posterior aspect of the capsule. The central part spirals superolaterally from the ischium, where it is attached posteroinferior to the acetabulum, then courses posterior to the femoral neck to attach distally to the greater trochanter deep to the iliofemoral ligament. Some fibres blend with the zona orbicularis. Some of the more inferior fibres of the ischiofemoral ligament embrace the posterior circumference of the femoral neck.
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