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Acquired cystic kidney disease following long-term peritoneal dialysis for congenital nephrotic syndrome.

Abstract
We describe here the clinicopathological findings in a child with congenital nephrotic syndrome (CNS) non-responsive to medical therapy who developed acquired cystic kidney disease (ACKD) in both native kidneys after long-term peritoneal dialysis. This case indicates that CNS is a further pathologic condition related to the development of ACKD.
AuthorsC Bosman, F Diomedi Camassei, F Del Nonno, A Corsi, R Boldrini
JournalScandinavian journal of urology and nephrology (Scand J Urol Nephrol) Vol. 36 Issue 1 Pg. 83-6 (Feb 2002) ISSN: 0036-5599 [Print] England
PMID12002366 (Publication Type: Case Reports, Journal Article)
Topics
  • Child
  • Glomerulosclerosis, Focal Segmental (complications, congenital)
  • Humans
  • Kidney (pathology)
  • Male
  • Nephrotic Syndrome (complications, congenital, therapy)
  • Peritoneal Dialysis
  • Polycystic Kidney Diseases (etiology, pathology)

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