Presentation
Family history of ADPKD.
Patient Data
Age: 45 years
Gender: Female
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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).