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

SA Journal of Radiology

 
 
Field Value
 
Title Polycystic liver disease - a disease entity presenting as part of autosomal-dominant polycystic kidney disease
 
Creator Boonzaaier-Botha, H. Cock, C.
 
Subject — —
Description 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 any organisms or malignant cells.A diagnosis of autosomal- dominant polycystic kidney disease was suspected, but could not initially be confirmed on ultrasound/ computed tomography imaging. Magnetic resonance imaging confirmed the multiple hepatic cysts and revealed multiple smaller cysts in both kidneys. Symptomatology subsided after aspiration of the largest cyst and the patient was discharged. The patient has subsequently been followed up and is currently symptom free. The case illustrates the importance of screening for associated kidney disease in patients with polycystic liver disease.
 
Publisher AOSIS
 
Contributor
Date 2004-06-09
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — —
Format application/pdf
Identifier 10.4102/sajr.v8i2.132
 
Source South African Journal of Radiology; Vol 8, No 2 (2004); 34 2078-6778 1027-202X
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://sajr.org.za/index.php/sajr/article/view/132/144
 
Coverage — — —
Rights Copyright (c) 2004 H. Boonzaaier-Botha, C. Cock https://creativecommons.org/licenses/by/4.0
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