2006, Number 3
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Bol Col Mex Urol 2006; 21 (3)
Enfermedad multiquística renal en el adulto. Reporte de caso y revisión de la literatura
Ávila HP, Beltrán SE, De Alba MA
Language: Spanish
References: 9
Page: 96-98
PDF size: 770.89 Kb.
ABSTRACT
Among cystic renal pathology, the multicystic dysplasic renal disease is found mainly in childhood, and it is with
the prenatal ultrasound that the diagnostic is achieved, however, in this case we found an example of multycistic
disease in the adult, associated to stenosis of the ureteropelvic junction, which only sympthom is the one given
by its mass effect.
REFERENCES
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Noam L, et al. Inisghts into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney disease. Prenatal Diagnosis 1999; 19(5).
Prasad P, Goodbole D, et al. Follow up after unilateral nephrectomy in children: is an estimate of glomerular filtration rate necessary? BJU International 2005; 95(4): 635-7.
Douglas M. Joubert syndrome associated with multicystic kidney disease and hepatic fibrosis. Pediatric Nephrology; 11(6): 746-9.
Fanos V, Schena S. Multicystic kidney dysplasia and turner syndrome: two cases and a literature review. Volume 14, numbers 8-9, pp 754-7.
Kuwertz E, Brinkmann A. Unilateral multicystic dysplastic kidney: experience in children. Volume 93, number 3, February 2004, pp 388-92.
Ambrosse SS. unilateral multicystic renal disease in adults 1976.
Reuss JWA. Sonographic, clinical and genetic aspects of prenatal diagnosis of cystic kidney disease. Ultrasound in Medicine and Biology 1991; 17(7): 687-94.
Castillo OA, Boyle ET. Multilocular cysts of kidney. Urology 1991; 37(2): 156-62. 10 Mullin E. Renal cystic disease. Urology 1976; 8(1): 5-8. 11.Elkin M. Cystic diseases of the kidney-radiological and pathological considerations. Clinical Radiology 1969; 20(1): 65-82.