Autosomal dominant polycystic kidney disease

Case contributed by David Cuete
Diagnosis certain

Presentation

Family history of ADPKD.

Patient Data

Age: 45 years
Gender: Female

CT abdomen and Pelvis

ct

There are innumerable cysts of varying sizes in the liver and kidneys with little remaining normal renal parenchyma. No evidence of hemorrhagic cysts.

Case Discussion

This case shows an autosomal dominant polycystic kidney disease (ADPKD) with extra-renal manifestation (liver).

ADPKD is the most common hereditary renal disease and is commonly associated with polycystic liver disease (75% of patients with ADPKD).

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