Abstract Background and Purpose: Autosomal dominant polycystic kidney disease (ADPKD)
manifests with renal and extrarenal abnormalities and is inherited in an autosomal dominant …

OBJECTIVES This study describes the natural history of patients with polycystic liver
disease, a rare disorder characterized by multiple hepatic cysts. METHODS Cases were …

Background Cyst infection is a severe complication of hepatic cystic disease. However, an
evidence‐based treatment strategy is not available. Aim To assess the available treatment …

In patients with autosomal dominant polycystic kidney disease (ADPKD), massive renal
enlargement is a serious problem. Renal transcatheter arterial embolization (TAE) can …

A total of 316 patients (167 men and 149 women) with autosomal dominant polycystic
kidney disease was studied retrospectively by a multi-institute group. With advancing patient …

Purpose To determine whether there is any difference in the prevalence of acquired cystic
disease and malignancy of the kidney in patients on continuous ambulatory peritoneal …

AIMS: Since 1979 the diseased kidneys of 96 patients on replacement therapy with chronic
renal failure due to chronic glomerulonephritis have been followed to investigate the …

Acquired renal cystic disease (ARCD) is defined as the development of multiple cysts in the
renal cortex and medulla in patients with chronic renal failure who are free from congenital …

OBJECTIVE. Localized cystic disease of the kidney is a benign nonsurgical condition. Its
imaging and clinical features are characterized and differentiated from autosomal dominant …

Background Autosomal dominant polycystic kidney disease (ADPKD) is an inherited
disorder that results in the growth of cysts in the kidneys and other organs. Multisystemic …