Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited
kidney disease causing endstage kidney disease (ESKD)[1] and currently has no cure …

Recurrent upper urinary tract (renal) infections have been reported to be frequent in patients
with autosomal dominant polycystic kidney disease and often difficult to treat. Female …

Dear Sir, Acquired cystic disease of the kidneys is a recognized complication among
patients with longstanding renal failure. It has been suggested the development of cysts is …

Key words: acute abdomen; autosomal dominant polycystic kidney disease; haemodialysis;
liver cyst rupture; polycystic liver disease [ABSTRACT FROM PUBLISHER] Copyright of …

Figure 1. A 45-year-old man with autosomal dominant polycystic kidney disease presented
to the urology clinic for consideration of bilateral nephrectomy as treatment for severe …

Background Autosomal dominant polycystic kidney disease (ADPKD) is the most common
hereditary cause of kidney failure. Peritoneal dialysis (PD) often is avoided because of …

A 28-year-old man diagnosed with autosomal dominant polycystic kidney disease (ADPKD)
was referred for further management. The patient was diagnosed at the age of 4, when he …

To characterize the syndrome of hepatic cyst infection in autosomal dominant polycystic
kidney disease (ADPKD) and to review its diagnosis and management, we retrospectively …

Fig. 1.(A) 40-year-old male patient, positive family history (mother with ADPKD),
hypertension and renal failure. Note numerous large uncomplicated cysts with demonstrable …

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