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Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection

Type 1 membranoproliferative glomerulonephritis (MPGN) is an immune complex-mediated disorder that has been associated with certain viral infections including hepatitis C, hepatitis B, hepatitis G, HIV and Hantavirus. We describe a patient with type 1 MPGN in native kidneys and nephrotic syndrome in...

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Autores principales: Karamadoukis, Lazarus, Toth, Tibor, Tomson, Charlie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421260/
https://www.ncbi.nlm.nih.gov/pubmed/25983923
http://dx.doi.org/10.1093/ndtplus/sfn098
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author Karamadoukis, Lazarus
Toth, Tibor
Tomson, Charlie
author_facet Karamadoukis, Lazarus
Toth, Tibor
Tomson, Charlie
author_sort Karamadoukis, Lazarus
collection PubMed
description Type 1 membranoproliferative glomerulonephritis (MPGN) is an immune complex-mediated disorder that has been associated with certain viral infections including hepatitis C, hepatitis B, hepatitis G, HIV and Hantavirus. We describe a patient with type 1 MPGN in native kidneys and nephrotic syndrome in whom there was strong evidence that a primary Epstein–Barr virus (EBV) infection played a causative role. This patient was treated with an angiotensin 2-receptor blocker and the nephrotic syndrome resolved within 6 months from presentation. Our case report suggests that MPGN presenting with nephrotic syndrome may have a relatively benign course when it is associated with an acute EBV infection.
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spelling pubmed-44212602015-05-15 Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection Karamadoukis, Lazarus Toth, Tibor Tomson, Charlie NDT Plus Case Report Type 1 membranoproliferative glomerulonephritis (MPGN) is an immune complex-mediated disorder that has been associated with certain viral infections including hepatitis C, hepatitis B, hepatitis G, HIV and Hantavirus. We describe a patient with type 1 MPGN in native kidneys and nephrotic syndrome in whom there was strong evidence that a primary Epstein–Barr virus (EBV) infection played a causative role. This patient was treated with an angiotensin 2-receptor blocker and the nephrotic syndrome resolved within 6 months from presentation. Our case report suggests that MPGN presenting with nephrotic syndrome may have a relatively benign course when it is associated with an acute EBV infection. Oxford University Press 2008-10 2008-07-04 /pmc/articles/PMC4421260/ /pubmed/25983923 http://dx.doi.org/10.1093/ndtplus/sfn098 Text en © The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Karamadoukis, Lazarus
Toth, Tibor
Tomson, Charlie
Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title_full Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title_fullStr Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title_full_unstemmed Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title_short Membranoproliferative glomerulonephritis associated with an Epstein–Barr virus infection
title_sort membranoproliferative glomerulonephritis associated with an epstein–barr virus infection
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421260/
https://www.ncbi.nlm.nih.gov/pubmed/25983923
http://dx.doi.org/10.1093/ndtplus/sfn098
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