Autosomal dominant polycystic kidney disease

Case contributed by Assoc Prof Frank Gaillard


Adult patient with renal failure.

Patient Data

Age: Adult

CT of the abdomen (coronal reformats) demonstrates both kidneys to be markedly enlarged by innumerable cysts ranging in size from a few millimeters to multiple centimeters. These cysts also vary in density: most are near-water density, some are hyperdense, others are calcified. 

Also present are numerous cysts in the liver. The pancreas is unremarkable.

Features are consistent with autosomal dominant polycystic kidney disease, which was subsequently confirmed. 

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Case information

rID: 5203
Published: 17th Dec 2008
Last edited: 13th Aug 2019
System: Urogenital
Tag: kidney
Inclusion in quiz mode: Included

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