Introduction

Clinical and Radiological Findings in Joint Disease

Condition Site of involvement Discriminatory findings
Primary osteoarthritis (F>M ▸ > 45 years) Hands PIP and DIP joint involvement (Heberden's and Bouchard's nodes) ▸ no osteopenia
Large joints (e.g. hip, knee) Joint space narrowing ▸ subchondral sclerosis ▸ subchondral cysts ▸ marginal osteophytes
Spine Degenerative disc disease ▸ spondylosis deformans ▸ apophyseal joint involvement ▸ spinal stenosis ▸ foraminal stenosis
Erosive osteoarthritis (affects middle-aged females) Hands PIP and DIP joint involvement ▸ joint ankylosis ▸ ‘gull-wing’ deformities (central erosions and marginal osteophytes)
Rheumatoid arthritis (F>M ▸ Rh factor positive) Hand and wrist Symmetrical arthritis ▸ MCP and PIP joint involvement ▸ periarticular (early) and diffuse (late) osteopenia ▸ marginal erosions ▸ subluxation (swan neck and boutonnière deformities) ▸ periostitis is uncommon
Large joints Joint space narrowing ▸ marginal erosions ▸ synovial cysts ▸ protrusio acetabulae
Spine Atlantoaxial subluxation
Juvenile idiopathic arthritis (M = F ▸ affects children) Hands Joint ankylosis ▸ florid periosteal reaction ▸ osteopenia
Large joints (e.g. knee) Abnormalities of growth and maturation ▸ epiphyseal overgrowth and premature closure of the physis ▸ widened intercondylar notch
Cervical spine Apophyseal joint fusion ▸ atlantoaxial subluxation
Psoriatic arthritis (M>F ▸ nail changes ▸ HLA-B27 +ve) Upper extremities (e.g. hands and feet) ‘Sausage’ digit ▸ DIP joint involvement ▸ terminal tuft erosion ▸ pencil-in-cup deformity ▸ joint ankylosis ▸ arthritis mutilans ▸ periosteal reaction ▸ no osteopenia
SI joints Asymmetric or unilateral sacroiliitis
Spine Coarse syndesmophytes
Reiter's syndrome (affects young male adults) Lower extremities (e.g. foot) Hallux involvement ▸ periosteal reaction ▸ calcaneal erosions ▸ osteopenia not prominent
Spine Coarse syndesmophytes
SI joints Asymmetric or unilateral sacroiliitis
Ankylosing spondylitis (M>F ▸ affects young adults ▸ HLA-B27 +ve in 95%) SI joints Bilateral symmetrical sacroiliitis ▸ ankylosis
Spine Anterior vertebral body squaring ▸ syndesmophytes ▸ paravertebral ossification ▸ bamboo spine
Pelvis ‘Whiskering’ of the iliac crests and ischial tuberosities
Enteropathic arthropathies SI joints Symmetrical sacroiliitis
Gout (M>F) Hands and feet (especially the great toe) MTP joint of the great toe ▸ juxta-articular erosions ▸ punched-out lesions with an overhanging margin ▸ no periarticular osteopenia ▸ tophi
CPPD crystal deposition disease (M = F) Any peripheral joint ▸ predilection for the knee Degenerative changes ▸ chondrocalcinosis ▸ paucity of subchondral sclerosis
HA crystal deposition disease (M = F) Predilection for the shoulder (supraspinatus tendon) Periarticular calcification
Haemochromatosis (M>F) Hands 2 nd and 3 rd MCP joint involvement (‘squared’ metacarpal heads) ▸ joint space narrowing ▸ ‘hook-like’ osteophytes ▸ numerous subchondral cysts
Alkaptonuria (ochronosis) (M = F) Intervertebral discs ▸ SI joints ▸ large joints Degenerative changes: disc calcification ▸ joint space narrowing ▸ periarticular sclerosis
Systemic lupus erythematosus (F>M ▸ affects young adults) Hands Reversible MCP joint subluxation
Scleroderma (F>M ▸ affects adults) Hands IP joint arthritis ▸ acro-osteolysis ▸ soft tissue calcifications
Mixed connective tissue disease (overlap syndrome) Hands PIP joint, MCP joint, mid-carpal involvement ▸ soft tissue swelling, calcifications or atrophy
Multicentric reticulohistiocytosis (F>M) Hands and feet DIP joint and carpal involvement ▸ soft tissue swelling ▸ articular erosions ▸ no osteopenia
Polymyositis / dermatomyositis Proximal extremities Soft tissue calcification
Hands DIP joint erosions
Sarcoidosis Distal and middle phalanges of the hands and feet Punched-out cyst-like lesions ▸ ‘lace-like’ appearance
Haemophilic arthropathy (affecting males – but with female carriers) Predilection for large joints (e.g. knee) Epiphyseal overgrowth ▸ juxta-articular osteopenia ▸ erosion and cartilage destruction ▸ widened intercondylar and trochlear notches ▸ squared patella
Neuropathic arthropathy Any joint 5 ‘D's’: normal bone D ensity ▸ joint D istension ▸ bony D ebris ▸ joint D isorganization ▸ D islocation
Hypertrophic osteoarthropathy Tubular bones (radius and ulna > tibia and fibula) Diaphyseal and metaphyseal painful periostitis

Osteoarthritis

Osteoarthritis

Definition

  • This is the most common joint disorder – it is a balance between degenerative joint destruction (stressed bone) and repair (non-stressed bone)

  • Primary OA: there is no underlying cause ▸ it occurs in the context of normal biomechanical forces

    • The joints most at risk: thumb base ▸ DIP joints ▸ acromioclavicular joints ▸ knees ▸ hips ▸ 1 st MTP joints ▸ spinal apophyseal joints

  • Secondary OA: joints are damaged by previous disease

    • Causes : trauma ▸ systemic, metabolic or endocrine disorders (e.g. rheumatoid arthritis, ochronosis, haemochromatosis) ▸ crystal deposition disease ▸ neuropathic disorders ▸ congenital hip dislocation ▸ bone dysplasias

Clinical Presentation

  • Pain ▸ reduced movement ▸ joint crepitus (± effusion) ▸ early morning stiffness

Radiological Features

Location

It is typically asymmetrical and affects the hands, spine and large weight-bearing joints ▸ primary and secondary OA have similar radiological appearances

XR

Localized joint space narrowing ▸ subchondral cysts and sclerosis ▸ marginal osteophytes ▸ loose bodies ▸ chondocalcinosis

  • Deformity and subluxation are uncommon ▸ osteoporosis and ankylosis are not features

Hand

The commonly affected joints: 1 st MCP joint, scaphotriquetral joint, IP joints ▸ distal and proximal IP joint prominences are commonly seen (Heberden's and Bouchard's nodes, respectively)

Knee

Tibial spine spiking is an early sign ▸ the medial joint compartment shows the greatest narrowing (as it is subject to greater stressors) leading to a varus deformity ▸ it usually affects the lateral facet of patellofemoral joint ▸ there is articular and meniscal cartilage chondrocalcinosis

  • Chondromalacia patellae: this is a related condition in younger patients with softening of the patellar cartilage (due to repetitive trauma)

  • Pellegrini–Stieda disease: ossification of the medial collateral ligament is associated with degenerative change or may occur in isolation

Hip

Loss of the superior weight-bearing joint space with marginal osteophytes, subchondral acetabular cysts (Egger's cyst) and sclerosis formation ▸ there is a tendency for superolateral femoral head subluxation (but there may be lateral restraining osteophytes) ▸ rarely medial migration can lead to protrusio acetabuli ▸ ‘buttressing’: osseous hypertrophy along the medial femoral neck

Foot/ankle

The 1st MTP joint is the most commonly affected site (and is associated with hallux valgus)

  • ‘Talar beak’: the talonavicular joint is also commonly involved with formation of a dorsal bone spur

Spine

See degenerative spinal disease Section 7 Chapter 6

Pearls

Erosive OA

This characteristically affects middle-aged women ▸ destructive changes outstrip productive changes and can mimic an erosive arthritis (such as psoriatic arthropathy)

XR

Central erosions and marginal osteophytes (a ‘gull wing’ pattern) affecting the PIP + DIP joints (although large joint involvement has been described)

  • Differential: psoriasis and rheumatoid arthritis – however these will have no 1 st CMC joint involvement and will have marginal (as opposed to central) erosions with no true osteophyte formation

Plain radiographic findings in primary osteoarthritis and corresponding underlying pathophysiological causes*
Radiological finding Pathological cause
Localized joint space narrowing Articular cartilage fibrillation, ulceration and erosion lead to changes in collagen and protein polysaccharide structure of cartilage. This results in reduced turgor
Subchondral bony sclerosis Increased osteoblastic activity resulting in new bone formation and increased cellularity of the subchondral bone
Osteophyte formation (most commonly marginal) Cartilage and bone proliferation and revascularization of remaining cartilage
Bone cysts and bone collapse Subchondral micro-fractures and passage of synovial fluid under pressure through the damaged cartilage to excavate a subchondral cyst
Gross deformity with subluxation Ligamentous laxity resulting from mechanical force applied after the distortion of capsular structures
Loose bodies Fragments of bone and cartilage become separated and, if not resorbed, become loose in the joint. They may reattach to the membrane, become vascularized and undergo endochondral ossification
Fibrocartilage or hyaline cartilage calcification This is usually due to calcium pyrophosphate deposition disease (CPPD). The reparative response is usually quite florid

Severe osteoarthritis of the hip. There is joint space narrowing which has occurred asymmetrically within the joint, in this case affecting the superior joint (the most common pattern of hip involvement). Note also subchondral cyst formation (black arrowheads) and osteophytosis (arrows). The osteophytes form a rim around the femoral head/neck junction and are superimposed over the neck visible as a sclerotic line (white arrowheads), which should not be mistaken for a fracture. **

Erosive osteoarthritis. DP radiograph: in addition to the typical osteoarthritis changes seen in multiple joints, including the thumb base carpometacarpal joint, there is erosive change seen at many of the interphalangeal joints. The majority of these are central in location (subchondral) and give rise to the characteristic ‘seagull wing’ appearance of the distal articular surface (seen for example at the index, middle and ring distal interphalangeal joints). **

Chondromalacia patellae. T2WI MRI demonstrates denuded cartilage on the medial patella facet, with cystic change in the underlying bone (arrows). *

Osteoarthritis with joint narrowing and osteophyte formation (Heberden's nodes). †

Schematic diagram showing typical joint changes associated with osteoarthritis.

Osteoarthritis. MRI demonstrates degenerative changes of the knee with an effusion, loss of the medial meniscus, marginal osteophytosis and a large loose body lying medially within the joint. †

Haemophilic and Neuropathic Arthropathies

Haemophilic Arthropathy

Definition

  • There is recurrent bleeding into a joint due to a deficiency of blood clotting factors ▸ the repeated intra-articular bleeding leads to villous synovial hypertrophy with the accumulation of haemosiderin within macrophages ▸ with recurrent bleeds there is no longer complete recovery (restricted joint motion/contractures/muscle atrophy)

    • Classic haemophilia (haemophilia A): X-linked recessive ▸ factor VIII deficiency

    • Christmas disease (haemophilia B): X-linked recessive ▸ factor IX deficiency

Clinical presentation

  • Painful and swollen joints ▸ joint deformities

  • It is only expressed in males (females can be carriers)

Radiological features

Location

It particularly affects the knee, elbow, ankle and shoulder ▸ small peripheral joints are rarely involved

XR

Hyperaemia causes epiphyseal overgrowth and accelerated maturation in the immature skeleton ▸ pannus similar to that in rheumatoid arthritis causes marginal erosions ▸ there is neither uniform nor symmetrical joint involvement

  • Acute: joint effusion and oedema

  • Chronic: juxta-articular osteoporosis resulting from haemorrhage and periarticular hyperaemia ▸ increased radio-opacity of the periarticular soft tissues and synovium (due to haemosiderin deposition) ▸ articular erosion and cartilage destruction (due to a thickened synovium) ▸ secondary osteoarthritis (subchondral cysts are common)

    • Knee: a widened intercondylar notch ▸ a squared patella ▸ enlarged femoral condyles ▸ it demonstrates similar appearances to juvenile rheumatoid arthritis

    • Elbow: an enlarged radial head, erosion of the trochlear notch and olecranon fossa

    • Hip osteonecrosis ▸ protrusio acetabuli ▸ slipped epiphysis ▸ coxa valga

  • 5 stages:

    • Stage I: soft tissue swelling (± joint effusion) ▸ normal joint surfaces

    • Stage II: stage I + periarticular osteoporosis ▸ epiphyseal overgrowth

    • Stage III: erosions, sclerosis and subchondral cysts ▸ the joint space is preserved

    • Stage IV: stage III + focal or diffuse joint space narrowing

    • Stage V: a stiff contracted joint with significant degenerative change

MRI

This can detect early synovial thickening and hypervascularity, and cartilaginous changes ▸ it can differentiate between acute and chronic soft tissue bleeding

  • T1WI/T2WI: a thickened and irregular synovium with fibrosis and haemosiderin deposition

    • Haemosiderin: this generates low SI foci, with a blooming artefact on gradient-echo (GE) sequences

Pearls

  • Septic arthritis is a rare complication of haemophilia

Intraosseous subperiosteal or soft tissue pseudotumours

These can develop following the encapsulation of episodes of repeated haemorrhage ▸ it occurs particularly within the femur and around the pelvis ▸ it presents as a painless expanding mass, with soft tissue and bone destruction ▸ can be calcified ▸ mural nodules are characteristic

MRI

T1WI: a low SI thick fibrous capsule ▸ T2WI: central high SI (due to blood breakdown products)

Classic radiographic findings in hemophilia. (A) Note squaring of inferior pole of the patella. (B) Enlarged femoral condyles. (C) Tibiotalar slant. ©35

Bleeding into the joints in haemophilia. AP XR demonstrating widened intercondylar notches, narrow joint spaces and erosive change. The right knee is more severely affected. *

Gradient echo (GE) MR images of the knee in a patient with advanced haemophilia. There is low signal abnormality in the synovium, secondary to hemosiderin deposition. GE images are the most sensitive to susceptibility, and this can be seen in the marked ‘blooming’ artefact. ©35

Neuropathic Arthropathy (Charcot Joint)

Definition

  • A destructive and productive articular abnormality following a loss of pain sensation and/or proprioception

Clinical presentation

  • Painless joint deformity and destruction on a background of neurological disease

Radiological features

Location

The distribution helps determine the cause (see table)

Atrophic form

This occurs early and is more acute ▸ resorption of the ends of affected bones results in sharp pointed ends ▸ there is an absence of osteoporosis, sclerosis, fragmentation or soft tissue debris ▸ it may lead to joint dislocation

Hypertrophic form

This occurs later with a slow progression ▸ it begins with a joint effusion ▸ the joint spaces are initially widened but then narrowed ▸ there is marked bony sclerosis (and no osteoporosis) ▸ fragmentation of the articular surfaces results in bony debris, which may later fuse into a large dense and well-organized corticated bony mass (± fusion with the underlying bone or dissection into the muscle planes) ▸ there is periosteal new bone formation ▸ subluxation and dislocation preceeds total joint disorganization ▸ pathological fractures can occur

  • 5 ‘D's’: normal bone D ensity ▸ joint D istension ▸ bony D ebris ▸ joint D isorganization ▸ D islocation

Pearl

  • Differential: the pseudoneuropathic form of CPPD

Syphilitic neuropathic arthropathy of the hip. There is destruction and fragmentation of the right femoral head leading to bony dislocation and joint disorganization. *

Acute neuropathic osteoarthropathy. (A) Sagittal, T1WI shows marginal erosions (arrowheads) at the Lisfranc joint and intertarsal joints. Note that the surrounding subcutaneous fat is preserved, a finding that would be unlikely in the setting of infection. (B) Sagittal, T2W, fat-suppressed MR image of the same patient shows bone marrow edema with extensive regional distribution around the Lisfranc and intertarsal joints that contain small effusions. ©35

Conditions associated with neuropathic arthropathy*
Condition Prevalence of arthropathy Joints most commonly affected
Congenital insensitivity to pain 100% Ankle, tarsal, knee, hip
Syringomyelia 20–50% Shoulder, elbow, wrist, cervical spine
Neurosyphilis 5–10% Knee, hip
Diabetes mellitus 1% Midfoot, forefoot
Alcohol related Rare Foot

Juvenile Idiopathic Arthritis and Dish

Juvenile Idiopathic Arthritis (JIA)

Definition

  • This is otherwise known as juvenile rheumatoid arthritis or juvenile chronic arthritis

  • It is an inflammatory disorder of the connective tissues characterized by joint swelling, pain and tenderness affecting ≥ 1 joints for at least 6 weeks in patients who are < 16 years of age

Clinical presentation

  • Acute systemic onset type (Still's disease): constitutional symptoms ▸ hepatosplenomegaly ▸ there is little joint involvement

  • Oligoarthritis: ≤ 4 joints involved during the 1 st 6 months, usually progressing to:

  • Polyarthritis: ≥ 5 joints involved (both presentations are equally common) ▸ there is often asymmetrical involvement of the peripheral joints

  • Systemic arthritis: arthritis + a systemic illness ▸ there can also be a psoriatic arthritis and an enthesitis-related arthritis

Radiological features

Location

Knee > wrist ▸ also involved: feet, shoulders, elbows and hips

Early

Soft tissue swelling ▸ synovitis ▸ synovial hyperplasia and pannus formation ▸ a widened joint space (secondary to an effusion) ▸ periarticular osteopenia

  • Initially there is cartilage preservation

Late

Epiphyseal overgrowth and premature closure of the physis (due to a prolonged synovitis and hyperaemia) ▸ cartilage loss ▸ there is often extensive ankylosis (affecting the CMC and mid-carpal joints) ▸ joint space narrowing

  • Bone erosions are uncommon

Peripheral joints

Marked radial head enlargement may be seen ▸ a widened intercondylar notch of the knee ▸ overtubulated diaphyses ▸ enlarged and osteoporotic epiphyses with compression fractures ▸ florid periosteal new bone formation within the phalanges, metacarpals and metatarsals (cf. RA) ▸ enlarged, irregular and squared carpal bones (due to erosion and repair)

  • Misalignment and subluxation are uncommon

Spine/sacroiliac joints

The cervical spine is the most commonly affected region (it is rare within the thoracolumbar spine or sacroiliac joints) ▸ atlantoaxial subluxation is common ▸ compression fractures ▸ scoliosis (with advanced disease)

  • There can be underdevelopment and block fusion of the vertebral bodies and intervertebral discs (due to disc and apophyseal joint ankylosis which can also mimic Klippel–Feil syndrome)

Pearls

  • Rheumatoid factor is positive in 10% of cases

  • Complications: leg length discrepancy due to growth plate disturbance ▸ contractures ▸ AVN (due to JIA or the resultant steroid therapy)

  • In some children isolated hip involvement with bilateral protrusio acetabuli has been documented

Wrist fusion in juvenile rheumatoid arthritis. Posteroanterior (PA) view of the wrist shows fusion at the second and third carpometacarpal joints (curved arrows). Some of the carpal bones (arrows) are also fused. ©34

JIA of the knee. There is secondary degenerative change with loss of joint space, subchondral sclerosis associated with epiphyseal overgrowth, and widening of the intercondylar notch. *

Lateral radiograph of the cervical spine. There is squaring of the vertebral bodies. Note the extensive ankylosis of the facet joints posteriorly and widening of the space anterior to the odontoid.

Diffuse Idiopathic Skeletal Hyperostosis (Dish) (Forestier's Disease)

Definition

    • Marked hyperostosis at multiple sites ▸ involvement typically at enthesis sites

  • A multifocal entity characterized by ‘flowing’ ligamentous spinal ossification involving ≧ 4 contiguous vertebrae with preservation of the underlying disc height (cf. degenerative disc disease)

  • There is no apophyseal or sacroiliac joint fusion (cf. ankylosing spondylitis) ▸ there is hyperostosis of certain ligamentous attachments

Clinical presentation

  • Asymptomatic ▸ back pain and stiffness ▸ tendinosis (commonly affecting the elbow and heel)

Radiological features

Spine

T7 to T12 are commonly affected (it is typically right sided as the pulsating aorta inhibits ossification on the left) ▸ ossification of the anterior longitudinal ligament is seen at the affected level (up to 2 cm)

  • New bone formation within the cervical spine can cause dysphagia

  • Ossification of the posterior longitudinal ligament can cause spinal stenosis

Extraspinal features

  • Enthesopathy: heel and elbow spurs and a whiskered pelvic appearance

  • Ossification: pelvic tendons and ligaments ▸ superior of the sacroiliac joints ▸ symphysis pubis ▸ calcaneus ▸ tarsal bones ▸ patella ▸ olecranon ▸ humerus ▸ hands

Pearl

  • DISH is a reaction to stress and not an arthritis as such

DISH. (A) Lateral and (B) AP XRs show bridging osteophytes at multiple levels, out of proportion to the degree of underlying degenerative change. *

DISH. CT demonstrating ossification of the posterior longitudinal ligament. †

Rheumatoid Arthritis

Rheumatoid Arthritis

Definition

  • An inflammatory polyarticular synovitis (with synovial hypertrophy) of unknown aetiology ▸ it is a multisystem disease, with a positive rheumatoid factor identified in the majority ▸ joint destruction with late disease

Clinical presentation

  • Joint pain ▸ morning stiffness ▸ symmetrical joint swelling ▸ rheumatoid nodules ▸ tendon rupture (F > M)

Radiological features

Location

A symmetrical polyarthritis of the small joints of the hands and feet > larger joints > axial skeleton (usually affecting the cervical spine)

  • Early: juxta-articular osteopenia ▸ symmetrical soft tissue swelling ▸ joint space widening ▸ tenosynovitis

  • Later: diffuse osteoporosis ▸ marginal erosions involving the bare area (the bone between the edge of the articular cartilage and the joint capsule attachment) ▸ joint space narrowing ▸ reduced soft tissue swelling ▸ subchondral cysts ▸ joint subluxation and dislocation ▸ joint ankylosis (this is uncommon but typically affects the carpus)

  • End stage: pancompartmental loss of the joint spaces ▸ resorption of the carpal bones and ‘arthritis mutilans’

Osteopenia

Early: periarticular ▸ late: it becomes generalized due to steroid use or limitation of movement

Joint space changes

Early widening (due to synovial hypertrophy, effusion or pannus interposition between the articular surfaces) is followed by narrowing (due to cartilage destruction by pannus) ▸ joint alignment abnormalities are caused by tendonitis, tendon rupture or synovitis weakening the capsule

Erosions

These are classic periarticular marginal erosions involving the ‘bare areas’ of bone ▸ they less commonly involve the larger joints but are often more destructive in nature due to the greater stresses involved

Periostitis

This is less commonly seen than with a seronegative arthropathy ▸ if present it is commoner within the feet

Soft tissue changes

Fusiform swelling (due to capsular distension and oedema) over the IP and MCP joints ▸ swelling over the ulnar styloid (due to local involvement of the extensor carpi ulnaris tendon sheath) ▸ distension of the knee joint capsule (due to lateral displacement of the normally barely visible fat planes adjacent to the distal femur) ▸ rheumatoid nodules

Hand

Proximal distribution (carpal/MCP/PIP joints) with sparing of the DIP joints (cf. OA and psoriatic arthritis) ▸ commonly affected sites: the 2 nd and 3 rd MCP joints (initially affecting the radial side – more distal erosions are less commonly seen) ▸ the ulnar and radial styloid processes ▸ the distal radioulnar joint and carpus

  • Ulnar deviation (due to MCP subluxation)

  • Volar subluxation and dislocation of the phalanges at the MCP joint

  • Rotary subluxation of the scaphoid and drift of the entire carpus in an ulnar (± volar) direction

  • Boutonnière deformity: proximal IP joint flexion and distal IP joint extension

  • Swan neck deformity: proximal IP joint extension and distal IP joint flexion

  • ‘Telescope’ fingers: phalangeal dislocation with subsequent shortening

Foot

Changes lag behind those in the hands ▸ disease initially involves the MTP joints (particularly the 4 th and 5 th ) with erosions on the bare areas of the metatarsal heads ▸ lateral phalangeal subluxation with PIP joint dorsiflexion deformities ▸ bony ankylosis with chronic disease

Hips

There is predominantly medial joint involvement (cf. superior joint involvement in OA) ▸ medial migration and acetabular resorption results in protrusio acetabuli

Shoulder

Lateral clavicular resorption ▸ upward subluxation of the humeral head

Spine

Disease usually affects the cervical spine (the thoracic and lumbar spine are rarely involved) ▸ cervical spine facet joint erosions may result in subluxation and nerve entrapment ▸ basilar invagination is a late feature

  • Atlantoaxial subluxation: this is due to cruciate ligament damage (separation in flexion of > 2.5 mm in adults or 5 mm in children is abnormal)

  • Odontoid erosion: this results from involvement of the synovial joint between the odontoid peg and cruciate ligament or involvement of the small bursa adjacent to the odontoid

  • Odontoid fracture: this is due due to erosions or osteopenia

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