Background Cyst infection remains a challenging issue in patients with autosomal dominant
polycystic kidney disease (ADPKD). In most patients, conventional imaging techniques are …

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

Renal cysts are commonly encountered in clinical practice. Although most cysts found on
routine imaging studies are benign, there must be an index of suspicion to exclude a …

Background The impact of renal and extrarenal manifestations of autosomal dominant
polycystic kidney disease (ADPKD) during chronic haemodialysis (HD) has never been …

We report a rare case of thrombosis in the inferior vena cava (IVC) due to enlarged cysts in
autosomal dominant polycystic kidney disease. A 71-year-old woman visited our hospital …

We review our own experience as well as pertinent literature on the outcome of renal
replacement therapy (RRT) in autosomal dominant polycystic kidney disease (ADPKD). Due …

Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary and progressive
renal disease. By the age of 65 years, 45% to 70% of patients with ADPKD reach end-stage …

Introduction Cyst infection is a known complication of autosomal dominant polycystic kidney
disease (ADPKD). Here, we describe incidence, risk factors, clinical presentation, and …

Cyst infection in autosomal dominant polycystic kidney disease (ADPKD) poses a difficult
diagnostic and therapeutic problem. We describe a serious indolent cyst infection due to …