Polycystic liver diseases (PLD) represent a group of genetic disorders in which cysts occur
in the liver (autosomal dominant polycystic liver disease) or in combination with cysts in the …

Cyst infection is a diagnostic challenge in patients with autosomal dominant polycystic
kidney disease (ADPKD) because of the lack of specific manifestations and limitations of …

Background and objectives: Cyst infection is a complex diagnostic and therapeutic issue in
patients with autosomal dominant polycystic kidney disease (ADPKD); however, published …

Background Cyst infection remains a challenging issue in patients with autosomal dominant
polycystic kidney disease (ADPKD). In most patients, conventional imaging techniques are …

Renal cysts, which arise from renal tubules, can be seen in a variety of hereditary and
nonhereditary entities. Common mechanisms associated with renal cyst formation include …

Introduction: Recurrent urinary tract infections (UTI) are a common clinical problem in kidney
transplant recipients. Due to the complex urological anatomy derived from the implantation …

The diagnosis of hepatic cyst infection is difficult in patients with autosomal dominant
polycystic kidney disease (ADPKD). We hypothesized that carbohydrate antigen 19-9 (CA …

Cyst infection is a common complication of autosomal dominant polycystic kidney disease
(ADPKD). Diagnosis is challenging with standard imaging techniques. We aimed to evaluate …

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder
characterized by the development of fluid-filled cysts in the kidneys. The primary cause of …

Positron-emission tomography/computed tomography (PET/CT) has improved cyst infection
(CI) management in autosomal dominant polycystic kidney disease (ADPKD). The …