IPLab:Lab 5:Polycystic Kidney Disease

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Clinical Summary

This 64-year-old white man had a history of hypertension, adult-onset diabetes, gouty arthritis, chronic obstructive pulmonary disease (COPD), and chronic anemia. The patient was in end-stage renal failure due to polycystic kidney disease and he required renal dialysis. His mother and a brother both died from renal complications.

His terminal admission was for congestive heart failure and ventricular tachycardia. He underwent a coronary artery bypass grafting (CABG) operation but two days after the operation he developed pneumonia and died.

At autopsy the kidneys were markedly enlarged. The right kidney weighed 1660 grams and the left kidney weighted 1780 grams.

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Virtual Microscopy

<peir-vm>IPLab5PolycysticKidney</peir-vm>

Study Questions

  • <spoiler text="What are the inheritance pattern and incidence of adult polycystic kidney disease?">Autosomal dominant.

Adult polycystic kidney disease occurs in approximately 1 out of 1000 people. A rare autosomal recessive polycystic kidney disease occurs in childhood (perinatal, infantile, neonatal, and juvenile subcategories) but this anomaly is genetically distinct from the adult variety.</spoiler>

  • <spoiler text="What is the significance of history of hypertension and uremic pericarditis in this patient?">People with polycystic kidney disease often develop hypertension, as do many patients with renal disease. Uremic pericarditis often occurs in people with kidney failure induced uremia.</spoiler>
  • <spoiler text="What are some of the other congenital anomalies that can be seen in people with polycystic kidney disease?">Asymptomatic polycystic liver disease is seen in 40% of these patients. Cysts can also occur, albeit infrequently, in the spleen, pancreas and lungs. These people also have a 10% to 30% incidence of berry aneurysms in the circle of Willis.</spoiler>

Additional Resources

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