Physical Address
304 North Cardinal St.
Dorchester Center, MA 02124
Urinary tract disorders are common and comprise a significant part of the workload of General Practitioners, general physicians, paediatricians and surgeons. Prostate disorders account for at least half of the work in urological surgery. The main conditions are benign prostatic enlargement (BPE) caused by prostatic hyperplasia, affecting about 10% of ageing males in Western countries, and prostatic carcinoma, which is now the second most common cancer in men worldwide and the commonest cancer diagnosed in men in developed countries. The remaining surgical disorders of kidney and urinary tract can be divided into five broad groups: tumours, stone disease ( urolithiasis ), infections, congenital abnormalities and finally, local and systemic disorders secondarily involving the urinary tract.
This chapter deals with the symptoms, signs, approach to investigation and diagnosis of urinary tract disease. The various disease entities are then discussed in the five following chapters.
Urinary symptoms may be caused by intrinsic disease of the urinary tract or by disease of other structures.
Outflow of urine from the kidney may become impeded by urinary tract obstruction, and this may secondarily interfere with renal function. Chronic obstruction to bladder outflow or bilateral upper tract obstruction may lead to renal failure, often without any localising symptoms.
BPE (also referred to as benign prostatic hyperplasia or BPH once the histology is known) is the most common prostatic disorder, and usually presents with symptoms of bladder outflow obstruction (i.e., hesitancy or straining to initiate voiding, poor flow, incomplete emptying or urinary retention) and sometimes with haematuria. Prostatic obstruction predisposes to bladder infections and stones secondary to incomplete bladder emptying, and the patient may present with the consequent symptoms.
Prostate cancer may present with bladder outflow obstruction similar to BPE or it may be discovered at an asymptomatic stage at a medical check-up, by digital rectal examination (DRE) or by a blood test (prostate specific antigen, PSA). Some cases are first diagnosed because of symptoms of metastases, such as bone pain.
Chronic prostatitis may be bacterial or abacterial and usually presents with a chronic perineal ache. In the acute form, bacterial prostatitis can present as a systemic illness (or even gram-negative sepsis) with urinary symptoms and an exquisitely tender prostate. Occasionally, a prostatic abscess develops.
The important urinary tract tumours, stone diseases and infections are outlined in Table 34.1 . Any of these may present with haematuria. Disorders which cause urinary stasis also predispose to urinary tract infection.
Disease | Pathophysiology | Clinical Features |
---|---|---|
Tumours | ||
Renal cell carcinoma —fairly common | Occurs in adults. Derived from renal tubular cells | Presents either incidentally (e.g., on CT scan) or with symptoms of haematuria, a mass, or constitutional signs, such as pyrexia or polycythaemia or is asymptomatic |
Nephroblastoma (Wilms tumour; see Ch. 51 )—rare | Developmental origin; usually diagnosed before age 5 years | Presents as an abnormal mass with or without pain and haematuria |
Urothelial carcinoma (UC) —common | May arise in transitional epithelium anywhere in urinary tract from pelvicalyceal system to urethra, but most common in bladder | Usually presents with haematuria. Predisposes to urinary tract infections. May cause ureteric obstruction |
Squamous cell carcinoma (SCC) —very rare | Arises in metaplastic squamous epithelium. Secondary to chronic stone or schistosomal irritation, especially in bladder. Also arises de novo in squamous epithelium of distal urethra | Bladder SCC is often asymptomatic until it reaches an advanced stage; tends to be muscle-invasive at presentation with urinary symptoms, infection, haematuria, and pain |
Adenocarcinoma of bladder —very rare | Arises from columnar epithelium of urachal remnant | Features include haematuria and urinary symptoms; around a third have lymph node metastases at presentation |
Stone Disease | ||
In general | Stones in situ may cause irritation of urinary tract epithelium | Present as pain or haematuria or recurrent infection |
Stones may develop in pelvicalyceal system or bladder. Pelvicalyceal stones can pass into the ureter—very common | Chronic—renal stones may cause chronic pelviureteric or ureteric obstruction either directly or by causing fibrotic strictures Acute—renal stones may cause ureteric obstruction as they pass down the tract |
Present with chronic pain (caused by back pressure) or recurrent infection Present as acute colicky pain often with renal tenderness (renal or ureteric colic). Infection may supervene, destroying the kidney if untreated |
Infections | ||
‘Common’ infections caused by bowel organisms | Infection develops either via bloodstream (haematogenous) or lower urinary tract stasis predisposes to infection | Typically, present with dysuria and frequency with or without haematuria. Any urinary tract abnormality or stasis predisposes to infection Ascending infection may cause pyelonephritis, that is, infection of kidney and renal pelvis |
Tuberculosis—uncommon | Kidney involvement via bloodstream from pulmonary or other primary disease. May spread via urine to ureters and bladder | May present as haematuria, persistent sterile pyuria, or as an incidental finding in pulmonary tuberculosis |
Urinary schistosomiasis (also known as bilharzia)—very common in some developing countries; probably the world’s most common cause of haematuria | Induces chronic inflammation and fibrosis in bladder wall leading to gross bladder distortion, stones and sometimes squamous cell carcinoma | Presents with haematuria and various symptoms of infection and bladder fibrosis |
Urethritis | Commonly caused by sexually transmitted infections, for example, gonococcus or Chlamydia | Presents with urethral discharge and dysuria |
Congenital abnormalities may involve the kidneys, ureters, bladder, urethra and genitalia, either alone or in combination. Most of the serious abnormalities are recognised antenatally by ultrasound, at birth or in early childhood. The exceptions are polycystic disease and medullary sponge kidney , which usually present in adulthood. Less serious congenital abnormalities, such as duplex systems, may predispose to urinary tract infections because of abnormal flow dynamics. These abnormalities may be discovered at any age during investigation of recurrent urinary infections. Congenital disorders, which present mainly in adulthood, are discussed in Chapter 39 and those presenting mainly in childhood in Chapter 51 .
The urinary tract sometimes becomes secondarily involved in local inflammatory conditions, such as Crohn disease or diverticular disease. Fistulae may form, resulting in passage of flatus and/or faeces in the urine (pneumaturia and faecuria). Pelvic tumours in women can present with urinary retention. Retroperitoneal fibrosis, diverticulitis, tumours of the prostate, cervix or colon, and sometimes aortic or iliac aneurysms may secondarily involve the ureters and cause upper urinary tract obstruction.
These fall into eight categories:
abdominal pain
passage of blood in the urine ( haematuria )
pain associated with micturition ( dysuria )
disorders of micturition, such as frequency or hesitancy
retention of urine (acute or chronic)
urinary incontinence
passage of bowel gas in the urine ( pneumaturia )
passage of blood in the semen ( haemospermia )
Urinary tract disorders may cause abdominal pain with or without urinary symptoms.
Both renal inflammation and stretching of the renal capsule cause pain in the renal angle, the posterior gap between the lowest rib and iliac crest. This area may also become tender to palpation or percussion. Renal stones, tumours or polycystic disease may cause dull and persistent loin pain even without obstruction.
In acute infections, such as pyelonephritis (affecting renal pelvis and kidney) or bladder infection, the pain is severe and is usually associated with systemic features and urinary tract symptoms.
Acute upper ureteric obstruction and distension of the pelvicalyceal system produce excruciating loin pain. The pain is colicky (resulting from powerful ureteric peristalsis) and often radiates to the hypochondrium (right or left upper quadrant of the abdomen) or groin ( Fig. 34.1 ). This pain is known as renal or ureteric colic . When obstruction is low in the ureter, the pain may radiate to the genitalia.
Pain originating in the bladder (e.g., in cystitis) is experienced in the suprapubic area. Pain may be referred to the penis or vulva if the bladder trigone is involved. In adults, urinary symptoms, such as dysuria and frequency, are usually present as well, but children may have no localising symptoms or complain only of pain, making the diagnosis less obvious. Dysuria is usually the predominant symptom of urethral disorders, but pain arising in the male urethra (e.g., in sexually transmitted infections) is usually referred to the tip of the penis. Finally, the pain of prostatic inflammation (prostatitis) is usually felt deep in the perineum. The prostate is tender on rectal examination.
Pain from other abdominal pathology may sometimes mimic pain arising from the urinary tract. Acute appendicitis may present with suprapubic pain, and biliary tract pain may be referred to the right thoracolumbar region, while posterior duodenal ulcers and pancreatic disease may cause pain in the central lumbar region. An expanding or leaking abdominal aortic aneurysm may sometimes mimic urinary tract disease, particularly if a ureter is compressed, causing flank pain, which can be mistaken for renal colic. Diseases of the thoracolumbar spine, such as metastatic cancer, tuberculosis, spondylosis and disc lesions may also simulate upper urinary tract disorders. Suspected renal colic with a local rash is usually caused by shingles (herpes zoster); the rash may not appear for several days after the onset of pain; perineal zoster may cause retention of urine. In women, pain arising from the ovaries or genital tract (e.g., pelvic inflammatory disease) may be confused with bladder pain.
Patients may notice blood or even clots in the urine ( frank or visible haematuria ) and this needs to be distinguished from vaginal bleeding. More often, blood is discovered on ‘dipstick’ testing or microscopy of a midstream urine specimen (microscopic or non-visible haematuria) . Haematuria is often episodic rather than persistent, whatever the cause. ‘Dipstick’ testing for haematuria is extremely sensitive and hence yields many false positive results.
Tumours are a common cause of visible and non-visible haematuria and must be suspected even if another possible cause is found. Haematuria from tumours is typically painless, although upper urinary tract bleeding can cause ‘clot colic’. However, carcinoma-in-situ of the bladder, a dysplastic condition with a high probability of progression to invasive carcinoma, usually presents with irritative voiding, dysuria, and haematuria, often with a finding of sterile pyuria (pus cell without proven bacteria) on urine testing. Irritation from infection or stones may also cause bleeding, but is usually accompanied by pain or dysuria. If the urethra is obstructed by prostatic enlargement, straining at micturition may cause bleeding from dilated veins at the bladder neck.
Trauma to a normal kidney may cause frank haematuria if substantial force has been applied, but non-visible haematuria is common after minor trauma in contact sports and rarely indicates significant injury. Enlarged kidneys are more susceptible to trauma, whatever the primary pathology. In hydronephrosis or polycystic kidneys, minor blunt trauma may cause gross haematuria.
Sometimes, urine becomes red with haemoglobin rather than blood. In young people this may be induced by vigorous exercise, such as jogging ( exercise haemoglobinuria and haematuria ). These patients are believed to have defective red cell membranes, which makes them more vulnerable to trauma. Exercise haemoglobinuria is self-limiting and requires no treatment.
Haematuria also occurs in renal parenchymal inflammation, such as glomerulonephritis or arteritis. Haematuria may be caused by microemboli impacting in the kidneys, as in atrial fibrillation or infective endocarditis. Any urinary tract disorder with a potential for haematuria is more likely to be revealed when a patient is on anticoagulant therapy or develops a bleeding diathesis.
The stage of micturition at which blood appears is sometimes diagnostically useful. Blood from the kidneys, ureters or bladder wall will completely mix with the urine, and be present throughout the urinary stream. Urethral bleeding may leak out independently of micturition, or be seen only at the beginning or end of the urinary stream. Blood arising from the bladder neck or posterior urethra may sometimes present as terminal haematuria. Gross bleeding may result in the passage of clots.
Haematuria on dipstick testing can be confirmed by urine microscopy for red blood cells, and checked for infection by culture and sensitivity. Microscopic haematuria may represent a noteworthy lesion anywhere in the urinary tract and must be taken seriously; however, a significant cause is found in only 5% to 25% of patients.
Dysuria describes pain or discomfort on micturition, often accompanied by difficulty in voiding. The pain is often described as ‘burning’ or ‘like passing shards of glass’. Any irritation of the urethra may cause dysuria. The most common cause is urinary tract infection, but recent urethral instrumentation or catheterisation can also cause dysuria.
The normal bladder has a capacity of 350 to 500 mL. When capacity is reached, there is a conscious perception of bladder fullness (mediated via the periaqueductal grey matter in the pons), and at a socially acceptable time, the voiding reflex is triggered via the pontine micturition centre in the brain stem. Micturition is normally initiated by sphincter relaxation coupled with detrusor contraction, and the bladder empties. There are seven common symptoms of disorders of micturition:
urinary frequency
nocturia
urgency
hesitancy
poor urinary stream
postmicturition dribbling
urinary incontinence
Features and common causes of these symptoms are summarised in Table 34.2 .
Symptom | Description | Causes |
---|---|---|
Urinary frequency | Frequent passage of small quantities of urine but with normal daily urine volume (unlike in polyuria) |
|
Nocturia | The need to pass urine at night, usually accompanied by frequency or polyuria |
|
Urgency | Sudden desire to void, may result in incontinence |
|
Hesitancy | Difficulty in initiating micturition |
|
Poor urinary stream | Slow or interrupted urine stream |
|
Postmicturition dribbling | Continuous flow of urine drops at the end of micturition and may amount to incontinence |
|
Urinary incontinence | Involuntary loss of urine |
|
These are divided into voiding (or obstructive) symptoms: hesitancy, poor stream, incomplete bladder emptying and terminal dribbling; and storage (or irritative) symptoms: frequency, nocturia, urgency and urge incontinence. Combinations of these symptoms can occur in prostatic obstruction; similar symptoms also occur in bladder neck obstruction, urethral stricture, bladder calculi and lower urinary tract infection. The severity of symptoms in men is assessed using the International Prostate Symptom Score (see Box 35.1 , p. 473).
Urinary retention is the inability to void when the bladder is full. It occurs when the sphincter is unable to relax or when there is a prostatic or urethral obstruction, and the causes may coexist. Less commonly, it can occur when the bladder smooth muscle (detrusor) is unable to generate a contraction. This is termed bladder underactivity and contributing causes include increasing age, neurological disorders (such as multiple sclerosis, spinal cord injury (SCI), Parkinson disease, stroke), diabetes, a consequence of prolonged bladder outlet obstruction or pelvic surgery, and as a side effect of medication (i.e., anticholinergic drugs used to relax the detrusor muscle in bladder overactivity).
Acute urinary retention is often very painful and occasionally occurs in normal individuals, usually males, particularly postoperatively, when fluid overload, drugs, pain, the supine posture, anxiety or embarrassment are responsible. Similar factors may precipitate an episode in men with asymptomatic prostatic enlargement. Occasionally, acute retention is caused by an obstructing blood clot ( clot retention ) or stone.
In females, acute urinary retention may also occur in pregnancy, if the enlarging uterus becomes wedged in the pelvis at about 14 weeks’ gestation. Large ovarian cysts or uterine fibroids may cause similar obstruction. Other possible causes include neurological disorders, such as sacral nerve injury, multiple sclerosis, and following stress incontinence surgery (which increases the resistance of the bladder outlet and urethra). Fowler syndrome is an uncommon condition, which presents in young women as acute urinary retention caused by an underactive bladder, but is caused by a hypercontractile, non-relaxing external urethral sphincter. It is associated with urethral or pelvic pain, which limits the ability to tolerate urethral catheterisation. Alternative options to drain the bladder include insertion of a suprapubic catheter, or formation of a Mitrofanoff channel, which uses the appendix to provide a route to pass a catheter from the umbilicus or abdominal wall directly into the bladder, bypassing the urethra. Sacral nerve neuromodulation techniques can also be used to relax the sphincter to allow spontaneous voiding.
Chronic retention is often painless and occurs with structural or functional abnormalities of bladder muscle or the sphincter mechanism. Less commonly, it is caused by persistent urethral obstruction. In chronic retention, voiding of urine is often incomplete. The problem progresses until the residual volume approaches maximum bladder capacity. Voiding then usually occurs by ‘overflow’ and the bladder usually becomes abnormally distended. When obstruction is prolonged and severe, the bladder muscle hypertrophies, bladder diverticula may develop, and back pressure on the kidneys can cause uraemia and renal failure (high-pressure chronic retention). At any stage, complete cessation of flow, that is, acute-on-chronic retention , may be precipitated by overfilling (often alcohol induced), urinary tract infection or constipation. The most common cause of chronic retention is bladder outlet obstruction caused by a hypertrophied bladder neck or prostatic enlargement. It may also be caused by lower spinal neurological problems, for example, central protrusion of lumbar intervertebral discs damaging the S2, 3, 4 detrusor muscle innervation.
Involuntary passage of urine is a distressing and socially debilitating symptom. During filling, the detrusor muscle relaxes so the intravesical pressure does not rise until bladder capacity is approached. Once the bladder is filled, voiding occurs by coordinated detrusor contraction and sphincter relaxation. Both are mediated via a spinal reflex at the level of S2, 3, 4. Superimposed on this system is an inhibitory mechanism under cortical (conscious) control, to delay voiding, if it is socially inappropriate. Conscious control, including nocturnal control, develops during early childhood. Night-time incontinence is known as nocturnal enuresis .
The pathophysiology of incontinence can be divided into categories based on disorders of structure and function, which are described later and summed up in Box 34.1 . Some disease processes may produce incontinence by more than one mechanism. Urinary incontinence can be caused by a known underlying neurological problem (i.e., ‘neurogenic’), or ‘idiopathic’ for non-neurogenic patients, or where the cause is unknown.
Become a Clinical Tree membership for Full access and enjoy Unlimited articles
If you are a member. Log in here