Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the
development of numerous renal cysts leading to kidney enlargement and chronic kidney …

Background Acute febrile abdomen represents a diagnostic challenge in patients with
autosomal dominant polycystic kidney disease (ADPKD). Although criteria have been …

Background Autosomal dominant polycystic kidney disease (ADPCKD) is an inherited
progressive, multisystem disorder characterised by innumerable renal cysts, hepatic cysts …

We read with interest the article ''The renal cyst infection caused by Salmonella enteritidis in
a patient with autosomal dominant polycystic kidney disease: how did this pathogen come …

A 56-year-old man with a medical history of autosomal dominant polycystic kidney disease
(ADPKD) and rightsided cadaveric kidney transplantation with homolateral nephrectomy in …

A 49-year-old man with adult polycystic kidney disease and chronic renal failure receiving
regular haemodialysis for 8 months presented with a 2 week history of abdomen pain, gross …

Liver cyst infection (LCI) is a rare but life-threatening complication of autosomal dominant
polycystic kidney disease (ADPKD)[1]. Its diagnosis remains problematic given the lack of …

Nephrolithiasis is an important manifestation of autosomal dominant polycystic kidney
disease (ADPKD), which occurs in approximately 20% of patients. It should always enter the …

Background and objectives Cyst infection and cyst hemorrhage are frequent and serious
complications of autosomal dominant polycystic kidney disease (ADPKD), often being …

Transient episodes of pain are common in autosomal dominant polycystic kidney disease
(ADPKD). A small fraction of patients have disabling chronic pain. In this review, we discuss …