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IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines

Immunoglobulin A (IgA) vasculitis nephritis (IgAVN) and IgA nephropathy (IgAN) share many pathological parallels and are viewed as related diseases by many groups. Current treatment guidelines remain vague, controversial, and without consensus, especially regarding the role of immunosuppressive medi...

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Autores principales: Al Harash, Abdalhamid, Saeli, Stephanie, Lucke, Michael, Arora, Swati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725550/
https://www.ncbi.nlm.nih.gov/pubmed/33343961
http://dx.doi.org/10.1155/2020/8863858
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author Al Harash, Abdalhamid
Saeli, Stephanie
Lucke, Michael
Arora, Swati
author_facet Al Harash, Abdalhamid
Saeli, Stephanie
Lucke, Michael
Arora, Swati
author_sort Al Harash, Abdalhamid
collection PubMed
description Immunoglobulin A (IgA) vasculitis nephritis (IgAVN) and IgA nephropathy (IgAN) share many pathological parallels and are viewed as related diseases by many groups. Current treatment guidelines remain vague, controversial, and without consensus, especially regarding the role of immunosuppressive medications. We present five cases of IgAVN encountered at our tertiary care center between 2016 and 2020, which were treated with different immunosuppression regimens. Infection was the leading cause of death in this series. These cases provide evidence that IgAVN should be distinguished from IgAN on a spectrum of IgA-associated glomerulonephritis. The outcomes presented herein suggest that the morbidity and systematic involvement IgAVN is greater than previously believed and that these substantial risks should be reflected in contemporary treatment guidelines.
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spelling pubmed-77255502020-12-17 IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines Al Harash, Abdalhamid Saeli, Stephanie Lucke, Michael Arora, Swati Case Rep Rheumatol Case Series Immunoglobulin A (IgA) vasculitis nephritis (IgAVN) and IgA nephropathy (IgAN) share many pathological parallels and are viewed as related diseases by many groups. Current treatment guidelines remain vague, controversial, and without consensus, especially regarding the role of immunosuppressive medications. We present five cases of IgAVN encountered at our tertiary care center between 2016 and 2020, which were treated with different immunosuppression regimens. Infection was the leading cause of death in this series. These cases provide evidence that IgAVN should be distinguished from IgAN on a spectrum of IgA-associated glomerulonephritis. The outcomes presented herein suggest that the morbidity and systematic involvement IgAVN is greater than previously believed and that these substantial risks should be reflected in contemporary treatment guidelines. Hindawi 2020-12-02 /pmc/articles/PMC7725550/ /pubmed/33343961 http://dx.doi.org/10.1155/2020/8863858 Text en Copyright © 2020 Abdalhamid Al Harash et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Al Harash, Abdalhamid
Saeli, Stephanie
Lucke, Michael
Arora, Swati
IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title_full IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title_fullStr IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title_full_unstemmed IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title_short IgA Vasculitis Nephritis: A Case Series and Comparison of Treatment Guidelines
title_sort iga vasculitis nephritis: a case series and comparison of treatment guidelines
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725550/
https://www.ncbi.nlm.nih.gov/pubmed/33343961
http://dx.doi.org/10.1155/2020/8863858
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