The differential diagnoses for CRCC include RCC with cystic change, hereditary leiomyomatosis manifesting as a cystic renal lesion, cystic nephroma, clear cell papillary RCC, and other cystic lesions ...

Acquired cystic kidney disease is a form of kidney disease where cysts develop in patients who have had chronic kidney disease for a number of years, or patients who have reached end-stage kidney ...

Autosomal-dominant polycystic kidney disease (ADPKD) is one of the most common genetic disorders, affecting one in every 1,000 people and responsible for up to ten percent of patients on dialysis ...

Background The proband, a 33-year-old woman, presented with renal cysts, mild renal failure and a renal tumor. One of the proband's two sons had hyperechogenic kidneys and the other had renal cortical ...

Computed tomography scans showing bilateral enhancing renal masses that proved to be oncocytomas upo In a single-center study, 24% of patients crossed over to treatment and 95% of patients were alive ...

Analyses of the chemical composition of fluid in 12 cysts of a polycystic kidney disclosed marked variations in the concentrations of selected cations, glucose, urea and creatinine. The concentrations ...

We identified 67 cases of CRCC, which represented 2.5% of the 2679 cases of RCC resected at our institution between January 2005 and April 2013; 217 out of all 2679 RCC patients had concurrent cystic ...

Acquired cystic kidney disease represents a condition where fluid-filled sacs (also known as renal cysts) develop in the kidney. These cysts tend to develop in the cortex and medulla regions of the ...

Polycystic kidney diseases are a leading cause of end-stage renal failure and a common indication for dialysis or renal transplantation. Recent advances have led to insights into mechanisms underlying ...