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Published in: Pediatric Nephrology 4/2012

01-04-2012 | Brief Report

Association of nephrotic syndrome with immune reconstitution inflammatory syndrome

Authors: Petra Lankisch, Hans-Jürgen Laws, Anne-Margret Wingen, Arndt Borkhardt, Tim Niehues, Jennifer Neubert

Published in: Pediatric Nephrology | Issue 4/2012

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Abstract

Background

Up to 50% of patients with severe immune deficiency experience an excessive inflammatory response called immune reconstitution inflammatory syndrome (IRIS) after the initiation of antiretroviral therapy (ART). IRIS has been observed after various opportunistic infections with pathogens such as mycobacteria, including Bacille Calmette–Guérin, cryptococci, human herpesvirus-8, non-Hodgkin's lymphoma, and progressive multifocal leukoencephalopathy. Non-acquired immune deficiency-defining illnesses can also deteriorate after commencement of ART. Renal IRIS has been reported in a few patients with mycobacterial infections, but to the best of our knowledge no cases of nephrotic syndrome and IRIS have been described.

Case-Diagnosis/Treatment

We report the case of an infant with human immunodeficiency virus-1 (HIV-1) infection, Pneumocystis pneumonia, and encephalopathy. During immune reconstitution the patient developed nephrotic syndrome. Treatment of nephrotic syndrome was initiated with prednisone, an angiotensin-converting enzyme inhibitor (lisinopril), and low-molecular-weight heparin. ART was continued, but only a low level of lopinavir/ritonavir could be achieved. There was no relapse of nephrotic syndrome during 10 months of follow-up.

Conclusions

Nephrotic syndrome may occur in infants during immune reconstitution and should not be overlooked.
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Metadata
Title
Association of nephrotic syndrome with immune reconstitution inflammatory syndrome
Authors
Petra Lankisch
Hans-Jürgen Laws
Anne-Margret Wingen
Arndt Borkhardt
Tim Niehues
Jennifer Neubert
Publication date
01-04-2012
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 4/2012
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-011-2069-5

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