Autosomal dominant polycystic kidney disease

Case contributed by A.Prof Frank Gaillard

Patient Data

Age: Adult
Gender: Male

Both kidneys are markedly enlarged and replaced by innumerable cysts, consistent with known and established autosomal dominant polycystic kidney disease. Extensive hepatic involvement with multiple cysts is also noted, with one particularly large cyst just below the right hemidiaphragm. The pancreas is unremarkable. 

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Case information

rID: 5202
Case created: 17th Dec 2008
Last edited: 16th May 2017
Inclusion in quiz mode: Excluded

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