Patient Data
Age: Adult
Gender: Male
From the case:
Autosomal dominant polycystic kidney disease
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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.
Case Discussion
Autosomal dominant polycystic kidney disease is usually striking and is accompanied frequently by hepatic cysts.