cystic kidney


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cys·tic kid·ney

a general term used to indicate a kidney that contains one or more cysts, including polycystic disease, solitary cyst, multiple simple cysts, and retention cysts (associated with parenchymal scarring).

cystic kidney

A kidney that has undergone cystic degeneration.
See: polycystic kidney disease
See also: kidney
References in periodicals archive ?
While further research and testing is still needed, the work of doctors Sayer and Miles demonstrate that the abnormal cells in patients with cystic kidney disease do respond positively to drug treatments.
Kristoffersson et al., "Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.," The Journal of Clinical Endocrinology & Metabolism, vol.
A, Acquired cystic kidney disease (ACKD)-associated renal cell carcinoma (RCC) with intratumoral oxalate crystals (arrows).
These were acute kidney injury, renal calculus disease, cystic kidney diseases, Malignancy, Glomerulonephritis, Ischemic nephropathy, chronic tubulointerstitial nephritis with distal RTA, Pyelonephritis.
Renal neoplasia and acquired cystic kidney disease in patients receiving long-term dialysis.
and 648.0), renal disease (ICD-9-CM codes 582-586, 5900), obesity (ICD-9-CM code 278), and cystic kidney disease (ICD-9-CM codes 753.1 and 753.10).
Constantinos Deltas, PhD, and Mr Gregory Papagregoriou, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus, in the next article focus on recent advances in the molecular biology and genetics of cystic kidney diseases and discuss the prospects and need for more widespread availability of laboratories for genetic testing.
Bunting, (29) in his review of cytogenesis, made the insightful comment that his 2 cases of cystic kidney disease differed morphologically and clinically from many previous reportedly cases.
This very task has become much faster and easier in most cases, although there are exceptions, such as the MCKD1 gene for medullary cystic kidney disease (MCKD) type 1, which remains stubbornly elusive (Figure 1 shows schematically the morbid cystic kidney chromosome map).
Earlier reports have depicted glomerular cysts and have portrayed similar cases of "congenital cystic kidney with glomerular cysts" (2,3,4) (Figure 1, A and B).
These kidneys can also develop acquired cystic kidney disease (ACKD), characterized by cystic dilatation of renal tubules, with an increasing incidence in parallel with the duration of dialysis (87% after 9 years).