In this issue of the Proceedings(pages 933 to 942), Telenti and associates describe the
clinical manifestations and treatment of infected he patic cysts in patients with autosomal …

A histomorphometric and clinico-pathologic analysis of 26 autopsy cases of autosomal
dominant polycystic kidney disease (ADPKD) showed that (1) the density of biliary …

Liver cysts were found in 46 (29 per cent) of 158 patients over 10 years of age with
documented autosomal dominant-type polycystic kidney disease (PKD) from 62 unrelated …

AUTOSOMAL DOMINANT polycystic kid-ney disease is a systemic disorder with cystic
manifestations in the kidneys, liver, pancreas, seminal vesicles, and meninges; its noncystic …

To characterize the syndrome of hepatic cyst infection in autosomal dominant polycystic
kidney disease (ADPKD) and to review its diagnosis and management, we retrospectively …

Hepatobiliary (intrahepatic and peribiliary) cysts have been described for patients with
autosomal dominant polycystic disease. The purpose of this study was to determine the …

Hepatic CT findings were analyzed in 44 patients with autosomal-dominant polycystic
kidney disease and were correlated with liver and renal function tests and liver, splenic, and …

Hepatic cysts are a major manifestation of autosomal dominant polycystic kidney disease.
This study examined 239 autosomal dominant polycystic kidney disease patients and 189 …

We evaluated the morphological and functional features of hepatic cyst epithelium in adult
autosomal dominant polycystic kidney disease (ADPKD). In six ADPKD patients, we …

The objective of this study was to investigate the prevalence of hepatic cysts by age and
gender in patients with early autosomal-dominant polycystic kidney disease (ADPKD) and to …