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Renal cystic disease

Current Opinion in Pediatrics, 1999
Renal cystic diseases constitute the most common genetic cause for end-stage renal disease in children and young adults. Recently, there has been rapid progress regarding the identification or chromosomal localization of some of the responsible disease genes.
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CYSTIC DISEASE OF THE RENAL PYRAMIDS

British Journal of Urology, 1961
SUMMARY An outline of the main features of cystic disease of the renal pyramids is given. A case is described which is unusual in that the cysts were easily demonstrable on retrograde pyelography.
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The Spectrum of Renal Cystic Diseases

Hospital Practice, 1988
Clinical presentation, site of the lesions, etiology and pathogenesis, and prognosis are all highly variable across the broad spectrum of renal cystic diseases. Perhaps the most significant addition to our recent knowledge is recognition of the genetic nature of many of these entities.
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Renal cystic disease—An overview

Seminars in Roentgenology, 1975
T HERE HAVE BEEN a number of classifications of renal cysts,2p6 and more will undoubtedly appear, indicating weaknesses in those already proposed. The major advantage of classification is to clear up the many confusions in terminology of the various types of renal cystic disease.
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Renal Medullary Cystic Disease

Acta Radiologica, 1988
Medullary cystic disease (MCD) is an uncommon renal disease with adult onset and autosomal inheritance, eventually progressing to terminal renal failure. It may be difficult to identify because of insufficient diagnostic tools. At urography, the same ring- shaped accumulation of contrast medium at the corticomedullary junction was observed in two ...
A, Olsen   +2 more
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Renal Cystic Disease

Ultrasound Clinics, 2010
Renal cystic disease is a heterogeneous entity, including developmental (simple and complex cysts, localized cystic diseases, extraparenchymal sinus cysts, medullary sponge kidney, and multicystic dysplastic kidney), acquired (acquired cystic kidney disease), and heritable (autosomal dominant polycystic kidney disease, autosomal recessive polycystic ...
Kyongtae T. Bae   +2 more
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Renal Cystic Diseases

2020
Renal cystic diseases may be inherited or acquired. The most common renal cystic disease is multicystic dysplastic kidney, which is essentially a nonfunctioning kidney. Most renal cysts and cystic diseases do not require intervention, with the exception of multilocular cystic nephroma. Cases of multilocular cystic nephroma cannot be differentiated from
Alexandra Rehfuss   +3 more
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Pathogenesis of Human Cystic Renal Disease

Annual Review of Medicine, 1988
Cystic diseases of the kidney are common, often progressive disorders. The best of several alternative hypotheses to explain their development cites tubular dilation and compression of adjacent tissue. The initiating event may involve focal proliferation of epithelial cells and a consequent increase in the resistance to flow along affected tubules ...
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Renal Cystic Disease

Seminars in ultrasound, CT, and MR, 1991
Cystic lesions are one of the most common abnormalities of the kidneys and are the most common asymptomatic space-occupying lesions (Lang 1973, 1980, 1986). While the vast majority of renal cysts are of the uncomplicated simple cyst variety, renal cystic disease comprises a heterogeneous group of developmental, acquired, and hereditary entities.
C K, Hayden, L E, Swischuk
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Renal Cystic Disease

1980
Renal cysts, particularly when they are multiple, tend to be regarded as developmental anomalies. It is important to recognize, however, that many renal cysts are acquired lesions. One or more renal cysts can be found at necropsy in about half of all subjects over 50 years of age, and their comparative rarity in children and young adults strongly ...
R. A. Risdon, D. R. Turner
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