Renal medullary cystic disease.

Autosomal Dominant Medullary Cystic Kidney Disease (ADMCKD)

Imaging in cystic renal disease.

The term “cystic kidneys” is used to describe a heterogeneous group of conditions characterised either by single/multiple cysts or abnormal kidneys with no obvious cysts as the kidney may appear hyperechoic (solid). Confusion has arisen because the terminology is imprecise at times and multiple cysts do not necessarily denote a heritable condition or specific syndrome. The disorders span all ag...

Renal Medullary Carcinoma; A Rare Entity

AbstractRenal medullary carcinoma (RMC) is an uncommon aggressive neoplasm of the kidney. RMC is biologically aggressive with a very poor prognosis, and metastasis is seen in up to 95% of the patients at diagnosis or shortly thereafter. The common sites of metastasis are respectively lymph nodes, lungs, livers, and adrenal glands in order of frequency. The presence of poorly differentiated eosi...

Rapidly Progressive Renal Dysfunction in Two Elderly Patients with Renal Enlargement and Medullary Cystic Kidney Disease-like Acute Tubulointerstitial Injury

Medullary cystic kidney disease (MCKD) is a hereditary disease associated with bilateral medullary polycysts and interstitial fibrosis. MCKD is typically associated with slowly progressive renal dysfunction. We herein report two rare elderly cases with enlarged kidneys and rapidly progressive renal dysfunction without myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA), PR3-ANCA, or...

Molecular genetics of nephronophthisis and medullary cystic kidney disease.

Nephronophthisis (NPH) and medullary cystic kidney disease (MCKD) constitute a group of renal cystic diseases that share the macroscopic feature of cyst development at the corticomedullary border of the kidneys. The disease variants also have in common a characteristic renal histologic triad of tubular basement membrane disintegration, tubular atrophy with cyst development, and interstitial cel...