Polycystic liver disease - a disease entity presenting as part of autosomal-dominant polycystic kidney disease

A 65-year-old man was referred to the Gastroenterology Department with complaints of longstanding upper abdominal discomfort and hepatomegaly. Ultrasound of the liver revealed a massively enlarged liver with multiple cystic areas. Aspiration of the largest cyst revealed 15 ml of yellow fluid without...

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Bibliographic Details
Main Authors: H. Boonzaaier-Botha, C. Cock
Format: Article
Language:English
Published: AOSIS 2004-06-01
Series:South African Journal of Radiology
Online Access:https://sajr.org.za/index.php/sajr/article/view/132