Polycystic Kidney Disease (PKD)
This familial disorder is the most significant of a number of renal cystic disorders . Inherited as an autosomal dominant trait with high penetrance, PKD is a relatively common cause of end-stage renal failure in the fourth and fifth decades of life. Virtually 100 per cent of persons inheriting the disorder will have cystic changes, but not necessarily renal failure, by age 80 years. A separate, infantile form of the disease occurs in association with congenital hepatic fibrosis and causes death from renal failure in the first year of life. In adults, benign multiple renal cysts may present a similar radiographic appearance but are not associated with renal dysfunction or failure.
Clinical manifestations of PKD rarely occur before the ages of 20 to 25 years. This accounts for the frequent passage of the genetic trait to offspring by asymptomatic, yet affected, individuals of child-bearing age. Nonspecific, dull lumbar pain is the most frequent initial symptom and usually occurs when the kidneys are sufficiently enlarged to be palpable on examination of the abdomen. Sharp, localized pain may result from cyst rupture or infection or from passage of a renal calcuius Microhematuria without RBC casts is frequently the initial sign of PKD; gross hematuria mav also occur.
Hypertension occurs commonly in PKD at early stages of the disease. Polycystic disease may thus be discovered in the course of evaluating hypertension in a young adult. Nocturia due to a urinary concentrating defect is often present at the time of diagnosis, and most patients are unable to conserve salt on a salt-restricted intake. Urinary tract infection and pyelonephritis are common complications. Up to one third of patients with polycystic renal disease have multiple, asymptomatic hepatic cysts, and cerebral aneurysms are more prevalent than in unaffected persons.
The diagnosis of polycystic kidney disease is made on the basis of radiographic evidence of multiple cysts distributed throughout the renal parenchyma. The nephrogram phase of intravenous urography (IVP) shows the lucent cysts surrounded by attenuated strands of functional renal tissue. Renal ultrasonography is another valuable tool in demonstrating the distribution and size of the cystic lesions. Both studies can be employed to screen younger (>16 years of age) family members of patients in order to identify the asymptomatic lesion at a time when genetic counseling may be useful. Failure to concentrate the urine above 800 mOsm/kg H20 after dehydration is highly predictive of PKD in adolescents at risk for the disorder.
Therapy for polycystic kidney disease is directed toward control of hypertension and prevention and early treatment of urinary tract infections. Nephrectomy is occasionally indicated for persistent gross hematuria or for an infected renal cyst. Decompressing cysts by surgical “unroofing” is associated with a high incidence of complications, including complete renal failure. End-stage renal failure is managed by either dialysis or transplantation. Bilateral nephrectomy may be required prior to transplant in patients with inordinately large kidneys or in those with a history of frequent or persistent urinary tract infection.
- CLINICAL MANIFESTATIONS OF MALABSORPTION
- LABORATORY TESTS TOR BILIRUBIN
- Sarcoidosis
- MOTOR DISORDERS OF THE ESOPHAGUS
- ARTERIOSCLEROSIS OBLITERANS
- Verapamil
- MEDIASTINAL DISEASE
- GLOMERULAR DISEASE
- RENAL PARENCHYMAL
- Community Acquired Pneumonia
- COMMON PRESENTING COMPLAINTS
- HYPERKINETIC PULMONARY HYPERTENSION
- Magnetic Resonance Imaging (MRI)
- Mixed Glomerulopathies
- LABORATORY TESTS OF LIVER FUNCTION AND DISEASE
- PRINCIPLES OF CARDIOPULMONARY RESUSCITATION
- MYOCARDIAL DISEASE - MYOCARDITIS
- Pathogenic Mechanisms - Mechanism of Injury
- LIMITATION OF MFARCT SIZE
- Hematuria
- ATRIAL RHYTHM DISTURBANCES
- CLINICAL MANIFESTATIONS OF ENDSTAGE RENAL DISEASE
- SUDDEN CARDIAC DEATH
- Renal Glycosuria
- PATHOPHYSIOLOGY OF ISCHEMIC HEART DISEASE
- Clinical Manifestations
- THE FAMILIAL POLYPOSIS SYNDROMES
- CARDIOMYOPATHY
- NORMAL BILIARY PHYSIOLOGY
- SCREENING TESTS OF HEPATOBILIARY DISEASE
- Other Cystic Diseases
- Proliferative Glomerulonephritis
- SPECIFIC CLINICAL DISORDERS
- Amyloidosis
- DIAGNOSTIC TECHNIQUES AND THEIR INDICATIONS - IMAGING PROCEDURES