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

Renal cysts look innocent enough. When they occur alone, as they commonly do in adults
over the age of 50 years, they do no harm. The handiwork of the aging process, some would …

Mutations in two different genes account for about 20% of cases with isolated liver cysts
(protein kinase C substrate, 80K-H, PRKCSH, and SEC63, which is a translocation protein …

The weight of evidence gathered from studies in humans with hereditary polycystic kidney
disease (PKD) 1 and PKD2 disorders, as well as from experimental animal models …

Background The enlarged cysts in autosomal dominant polycystic kidney disease (ADPKD)
frequently cause abdominal discomfort. Cyst sclerotherapy with minocycline hydrochloride …

The occurrence of acquired cysts in kidneys with primary chronic renal disease, particularly
tubulointerstitial diseases w1±3x, had been known in the 19th century but was forgotten, and …

Acquired renal cystic disease is common in patients receiving dialysis. Characteristically, the
kidneys are small or, less often, normal in size, and the cysts are usually less than 0.6 cm in …

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a systemic
hereditary disorder characterized by bilateral diffuse renal cysts. Extrarenal involvement is a …

Autosomal dominant polycystic kidney disease (ADPKD) is generally a late-onset
multisystem disorder characterized by bilateral kidney cysts, liver cysts, and an increased …

A 76-year-old man with autosomal dominant polycystic kidney disease (ADPKD) was
admitted complaining of severe edema of bilateral lower extremities. Computed tomography …