Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature

Podocyte infolding glomerulopathy (PIG) is a rare pathological finding that has gained more recognition recently. Most of the reported cases have been associated with connective tissue diseases especially systemic lupus erythematosus (SLE). Here we report the first case of Infolding Glomerulopathy a...

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Autores principales: Hijazi, Mohamad, Aboursheid, Tarek, Al Termanini, Mohammad, Khanjar, Izzat A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764042/
https://www.ncbi.nlm.nih.gov/pubmed/36545554
http://dx.doi.org/10.1002/ccr3.6756
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author Hijazi, Mohamad
Aboursheid, Tarek
Al Termanini, Mohammad
Khanjar, Izzat A. M.
author_facet Hijazi, Mohamad
Aboursheid, Tarek
Al Termanini, Mohammad
Khanjar, Izzat A. M.
author_sort Hijazi, Mohamad
collection PubMed
description Podocyte infolding glomerulopathy (PIG) is a rare pathological finding that has gained more recognition recently. Most of the reported cases have been associated with connective tissue diseases especially systemic lupus erythematosus (SLE). Here we report the first case of Infolding Glomerulopathy associated with SLE in the Middle East.
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spelling pubmed-97640422022-12-20 Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature Hijazi, Mohamad Aboursheid, Tarek Al Termanini, Mohammad Khanjar, Izzat A. M. Clin Case Rep Case Report Podocyte infolding glomerulopathy (PIG) is a rare pathological finding that has gained more recognition recently. Most of the reported cases have been associated with connective tissue diseases especially systemic lupus erythematosus (SLE). Here we report the first case of Infolding Glomerulopathy associated with SLE in the Middle East. John Wiley and Sons Inc. 2022-12-20 /pmc/articles/PMC9764042/ /pubmed/36545554 http://dx.doi.org/10.1002/ccr3.6756 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hijazi, Mohamad
Aboursheid, Tarek
Al Termanini, Mohammad
Khanjar, Izzat A. M.
Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title_full Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title_fullStr Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title_full_unstemmed Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title_short Podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: A case report and review of literature
title_sort podocyte infolding glomerulopathy after 25 years of clinical remission of lupus nephritis in a patient with systemic lupus erythematosus: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764042/
https://www.ncbi.nlm.nih.gov/pubmed/36545554
http://dx.doi.org/10.1002/ccr3.6756
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