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Apheresis Therapy for Steroid-Resistant Idiopathic Nephrotic Syndrome: Report on a Case Series.

Authors :
Naciri Bennani H
Jouve T
Noble J
Rostaing L
Malvezzi P
Tetaz R
Source :
Case reports in nephrology [Case Rep Nephrol] 2019 Oct 09; Vol. 2019, pp. 7304786. Date of Electronic Publication: 2019 Oct 09 (Print Publication: 2019).
Publication Year :
2019

Abstract

Idiopathic nephrotic syndrome (INS) represents 15%-30% of adulthood glomerulopathies. Corticosteroids have been the main treatment for decades and are effective in 70% of minimal-change disease patients and ~30% of focal segmental glomerulosclerosis patients. Multidrug-resistant (steroids, calcineurin-inhibitors, cyclophosphamide, mycophenolate-mofetil, rituximab) idiopathic nephrotic syndrome is a major therapeutic challenge in nephrology. Apheresis (double-filtration plasmapheresis or semi specific immunoadsorption) could act by eliminating the circulating factor (apolipoproteinA1b, solubleCD40L, suPAR) increasing glomerular permeability seen in INS. The aim of the study was to report the outcome of three patients with multidrug-resistant INS treated successfully with apheresis.<br />Competing Interests: The authors declare that they have no conflicts of interest.<br /> (Copyright © 2019 Hamza Naciri Bennani et al.)

Details

Language :
English
ISSN :
2090-6641
Volume :
2019
Database :
MEDLINE
Journal :
Case reports in nephrology
Publication Type :
Academic Journal
Accession number :
31687235
Full Text :
https://doi.org/10.1155/2019/7304786