L. Rosenfeld et al., Complicated polycystic liver disease with intracystic hemorrhage and obstructive jaundice, GASTRO CL B, 25(8-9), 2001, pp. 818-822
Polycystic liver disease, which is generally part of the autosomal dominant
polycystic kidney disease, is often asymptomatic. We report a case of obst
ructive jaundice caused by compression of the biliary tract by a large haem
orrhagic liver cyst. The patient was a man with sporadic polycystic liver d
isease without polycystic kidney. disease and with normal renal function fo
r his age. Ultrasound combined with cholangio-MRI provided non-invasive con
firmation of intracystic bleeding and intrahepatic biliary dilatation. Obst
ructive jaundice was confirmed by cyst puncture-aspiration which resolved s
ymptoms and normalized biology. The initial treatment of haemorrhagic liver
cyst complicating polycystic liver disease must be medical with cyst aspir
ation-drainage and sclerotherapy to avoid surgery in these fragile patients
.