Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy

We report a case of IgG4-related disease (IgG4-RD) diagnosed after 3 years of follow-up for idiopathic membranous nephropathy (MN). MN has been considered as glomerular lesion of IgG4-related kidney diseases in recent years and was diagnosed simultaneously with or after a diagnosis of IgG4-RD in pre...

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Autores principales: Wada, Yoko, Saeki, Takako, Yoshita, Kazuhiro, Ayalon, Rivka, Kamimura, Kenya, Nakano, Masaaki, Narita, Ichiei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Original Contributions
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779618/
https://www.ncbi.nlm.nih.gov/pubmed/24058729
http://dx.doi.org/10.1093/ckj/sft062
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author Wada, Yoko
Saeki, Takako
Yoshita, Kazuhiro
Ayalon, Rivka
Kamimura, Kenya
Nakano, Masaaki
Narita, Ichiei
author_facet Wada, Yoko
Saeki, Takako
Yoshita, Kazuhiro
Ayalon, Rivka
Kamimura, Kenya
Nakano, Masaaki
Narita, Ichiei
author_sort Wada, Yoko
collection PubMed
description We report a case of IgG4-related disease (IgG4-RD) diagnosed after 3 years of follow-up for idiopathic membranous nephropathy (MN). MN has been considered as glomerular lesion of IgG4-related kidney diseases in recent years and was diagnosed simultaneously with or after a diagnosis of IgG4-RD in previously reported cases. In the present case, IgG4-RD developed 3 years after the diagnosis of idiopathic MN, indicating a possible relationship between idiopathic MN and IgG4-RD through common underlying mechanisms of development.
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spelling pubmed-37796182014-10-01 Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy Wada, Yoko Saeki, Takako Yoshita, Kazuhiro Ayalon, Rivka Kamimura, Kenya Nakano, Masaaki Narita, Ichiei Clin Kidney J Original Contributions We report a case of IgG4-related disease (IgG4-RD) diagnosed after 3 years of follow-up for idiopathic membranous nephropathy (MN). MN has been considered as glomerular lesion of IgG4-related kidney diseases in recent years and was diagnosed simultaneously with or after a diagnosis of IgG4-RD in previously reported cases. In the present case, IgG4-RD developed 3 years after the diagnosis of idiopathic MN, indicating a possible relationship between idiopathic MN and IgG4-RD through common underlying mechanisms of development. Oxford University Press 2013-10 2013-08-13 /pmc/articles/PMC3779618/ /pubmed/24058729 http://dx.doi.org/10.1093/ckj/sft062 Text en © The Author 2013. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For permissions, please email: journals.permissions@oup.com. 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 Original Contributions
Wada, Yoko
Saeki, Takako
Yoshita, Kazuhiro
Ayalon, Rivka
Kamimura, Kenya
Nakano, Masaaki
Narita, Ichiei
Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title_full Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title_fullStr Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title_full_unstemmed Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title_short Development of IgG4-related disease in a patient diagnosed with idiopathic membranous nephropathy
title_sort development of igg4-related disease in a patient diagnosed with idiopathic membranous nephropathy
topic Original Contributions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779618/
https://www.ncbi.nlm.nih.gov/pubmed/24058729
http://dx.doi.org/10.1093/ckj/sft062
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