Liver involvement is the most frequent extrarenal manifestation in autosomal-dominant
polycystic kidney disease (ADPKD). Liver cysts are responsible for most hepatic …

Background Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder
characterised by progressive renal cyst formation leading to renal failure in the majority of …

Autosomal-dominant polycystic kidney disease (ADPKD) is a systemic disease, marked by
progressive increase of bilateral renal cysts, resulting in chronic kidney disease (CKD) and …

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 …

Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder.
Although liver involvement is the most frequent extra-renal manifestation, serious …

Background: There is a perception that patients with autosomal dominant polycystic kidney
disease (ADPKD) are more likely to develop kidney stones than the general population …

Infection of renal or hepatic cyst is a serious complication of autosomal dominant polycystic
kidney disease (ADPKD) and early diagnosis is crucial for the correct management. We …

In the new millennium, few kidney diseases changed their perspectives as much as
autosomal dominant polycystic kidney disease (ADPKD). New diagnostic approaches …

Background: Polycystic liver disease (PLD) is present in most patients with autosomal
dominant polycystic kidney disease (ADPKD). PLD can alternatively be found with few, if …

Background Cyst infection is a common and serious complication of autosomal dominant
polycystic kidney disease (ADPKD) that is often refractory. Carbapenems are frequently …