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A case of Podocytic Infolding Glomerulopathy with SLE and literature review
BACKGROUND: Podocytic infolding glomerulopathy (PIG) is a rare pathological change which was characterized by the microspheres or microtubular structures in the thickened glomerular basement membrane (GBM). Only a few dozen cases have been reported worldwide so far. Here we present a case of PIG wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665562/ https://www.ncbi.nlm.nih.gov/pubmed/34895156 http://dx.doi.org/10.1186/s12882-021-02615-4 |
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author | Liu, Xi Huang, Jieli Zhang, Kun Niu, Yangyang Liu, Yuting Cui, Chunli Yu, Chen |
author_facet | Liu, Xi Huang, Jieli Zhang, Kun Niu, Yangyang Liu, Yuting Cui, Chunli Yu, Chen |
author_sort | Liu, Xi |
collection | PubMed |
description | BACKGROUND: Podocytic infolding glomerulopathy (PIG) is a rare pathological change which was characterized by the microspheres or microtubular structures in the thickened glomerular basement membrane (GBM). Only a few dozen cases have been reported worldwide so far. Here we present a case of PIG with systemic lupus erythematosus. CASE PRESENTATION: A 61-year-old Chinese female was diagnosed with systemic lupus erythematosus with clinical manifestations of proteinuria, pleural effusion, seroperitoneum, anemia, leukopenia, thrombocytopenia, antinuclear antibody positive, and hypocomplementemia. She also had benign ovarian tumor and Epstein-Barr virus infection. Renal biopsy immunofluorescent staining showed IgM and C3 were granularly deposited along the capillary wall instead of typical “full house” features. Electron microscopy showed lots of microspheres structures were seen in the thickened GBM. CONCLUSION: We present a case of PIG in a patient with systemic lupus erythematosus. The mechanisms of PIG are unknown, but may be associated with connective tissue disease and podocyte injury. |
format | Online Article Text |
id | pubmed-8665562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86655622021-12-13 A case of Podocytic Infolding Glomerulopathy with SLE and literature review Liu, Xi Huang, Jieli Zhang, Kun Niu, Yangyang Liu, Yuting Cui, Chunli Yu, Chen BMC Nephrol Case Report BACKGROUND: Podocytic infolding glomerulopathy (PIG) is a rare pathological change which was characterized by the microspheres or microtubular structures in the thickened glomerular basement membrane (GBM). Only a few dozen cases have been reported worldwide so far. Here we present a case of PIG with systemic lupus erythematosus. CASE PRESENTATION: A 61-year-old Chinese female was diagnosed with systemic lupus erythematosus with clinical manifestations of proteinuria, pleural effusion, seroperitoneum, anemia, leukopenia, thrombocytopenia, antinuclear antibody positive, and hypocomplementemia. She also had benign ovarian tumor and Epstein-Barr virus infection. Renal biopsy immunofluorescent staining showed IgM and C3 were granularly deposited along the capillary wall instead of typical “full house” features. Electron microscopy showed lots of microspheres structures were seen in the thickened GBM. CONCLUSION: We present a case of PIG in a patient with systemic lupus erythematosus. The mechanisms of PIG are unknown, but may be associated with connective tissue disease and podocyte injury. BioMed Central 2021-12-11 /pmc/articles/PMC8665562/ /pubmed/34895156 http://dx.doi.org/10.1186/s12882-021-02615-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Liu, Xi Huang, Jieli Zhang, Kun Niu, Yangyang Liu, Yuting Cui, Chunli Yu, Chen A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title | A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title_full | A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title_fullStr | A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title_full_unstemmed | A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title_short | A case of Podocytic Infolding Glomerulopathy with SLE and literature review |
title_sort | case of podocytic infolding glomerulopathy with sle and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665562/ https://www.ncbi.nlm.nih.gov/pubmed/34895156 http://dx.doi.org/10.1186/s12882-021-02615-4 |
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