Cover image of the article: Acute Renal Failure in a Child with Idiopathic Nephritic Syndrome (A Case Study)

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Acute Renal Failure in a Child with Idiopathic Nephritic Syndrome (A Case Study)

Authors

AA Niki Bakhsh1,*, H Mahmoudzadeh1, M Karamiyar1, B Ilkhanizadeh1
1Iran
*Corresponding Author: Corresponding author: AA Niki Bakhsh, Iran, E-mail: Email: journal@kums.ac.ir

Journal of Kermanshah University of Medical Sciences:Vol. 10, issue 3; e81818
Published online:Dec 19, 2006
Article type:Case Report
Received:Jul 07, 2018
Accepted:May 30, 2006
How to Cite:Niki Bakhsh A, Mahmoudzadeh H, Karamiyar M, Ilkhanizadeh B. Acute Renal Failure in a Child with Idiopathic Nephritic Syndrome (A Case Study). J Kermanshah Univ Med Sci. 2006;10(3):e81818. doi:

Abstract

Introduction: Acute renal failure is an uncommon complication of idiopathic nephritic syndrome in children. Renal failure could be secondary to causes such as sever hypovolumia, acute tubular necrosis, interstitial nephritis, bilateral renal vein thrombosis, acute pyelonephritis and rapid progression of original glomerular disease. It may be idiopathic if the underlying cause is undetermined. Although idiopathic acute renal failure (IARF) has been described previously, this study presents histopathologic finding and outcome of IARF in a child with idiopathic nephritic syndrome.

Case Report: An 11 year - old girl with corticosteroid and cyclophosphamid resistant nephritic syndrome presented with acute renal failure. She was on cyclosporine one year ago but had relative response to cyclosporine, which presented with irreversible acute renal failure.

Discussion: IARF is a rare complication in children with idiopathic minimal change nephritic syndrome. The exact pathophysology of IARF is not well understood. Possible proposed explanations included severe interstitial oedema, peritonitis, hypovolemia, tubular obstruction, and altered glomerular permeability. In this case there is no justifiable cause for acute renal failure and IARF should be considered as a diagnostic possibility in this patient.

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© 2006, Journal of Kermanshah University of Medical Sciences. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

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