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A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis
Podocytic infolding glomerulopathy (PIG) has been proposed as a new disease entity. A 14-year-old girl underwent renal biopsy at our institution because of a chance finding of proteinuria. Light microscopic findings revealed a minor glomerular abnormality, but under a higher magnification, after per...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770251/ https://www.ncbi.nlm.nih.gov/pubmed/24027576 http://dx.doi.org/10.1159/000354591 |
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author | Iguchi, Akira Sohma, Ayako Yamazaki, Hajime Ito, Tomoyuki Saeki, Takako Ito, Yumi Imai, Naohumi Osawa, Yutaka Narita, Ichiei |
author_facet | Iguchi, Akira Sohma, Ayako Yamazaki, Hajime Ito, Tomoyuki Saeki, Takako Ito, Yumi Imai, Naohumi Osawa, Yutaka Narita, Ichiei |
author_sort | Iguchi, Akira |
collection | PubMed |
description | Podocytic infolding glomerulopathy (PIG) has been proposed as a new disease entity. A 14-year-old girl underwent renal biopsy at our institution because of a chance finding of proteinuria. Light microscopic findings revealed a minor glomerular abnormality, but under a higher magnification, after periodic acid methenamine silver staining, a bubbling appearance in the glomerular basement membrane (GBM) was observed. An electron microscopic examination revealed microspheres in the GBM, which were sparse but global. The patient was diagnosed as having PIG. After 3 years, her urinary protein had increased and a second biopsy was performed, showing focal segmental glomerulosclerosis in addition to a lesser degree of podocytic infolding than at the first biopsy. This is the first report of a case complicated by a different type of glomerulonephritis after being diagnosed as PIG. A few cases of PIG are complicated by focal segmental glomerulosclerosis, suggesting several mechanisms for the disorder. |
format | Online Article Text |
id | pubmed-3770251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-37702512013-09-11 A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis Iguchi, Akira Sohma, Ayako Yamazaki, Hajime Ito, Tomoyuki Saeki, Takako Ito, Yumi Imai, Naohumi Osawa, Yutaka Narita, Ichiei Case Rep Nephrol Urol Published online: August, 2013 Podocytic infolding glomerulopathy (PIG) has been proposed as a new disease entity. A 14-year-old girl underwent renal biopsy at our institution because of a chance finding of proteinuria. Light microscopic findings revealed a minor glomerular abnormality, but under a higher magnification, after periodic acid methenamine silver staining, a bubbling appearance in the glomerular basement membrane (GBM) was observed. An electron microscopic examination revealed microspheres in the GBM, which were sparse but global. The patient was diagnosed as having PIG. After 3 years, her urinary protein had increased and a second biopsy was performed, showing focal segmental glomerulosclerosis in addition to a lesser degree of podocytic infolding than at the first biopsy. This is the first report of a case complicated by a different type of glomerulonephritis after being diagnosed as PIG. A few cases of PIG are complicated by focal segmental glomerulosclerosis, suggesting several mechanisms for the disorder. S. Karger AG 2013-08-08 /pmc/articles/PMC3770251/ /pubmed/24027576 http://dx.doi.org/10.1159/000354591 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Published online: August, 2013 Iguchi, Akira Sohma, Ayako Yamazaki, Hajime Ito, Tomoyuki Saeki, Takako Ito, Yumi Imai, Naohumi Osawa, Yutaka Narita, Ichiei A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title | A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title_full | A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title_fullStr | A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title_full_unstemmed | A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title_short | A Case of Podocytic Infolding Glomerulopathy with Focal Segmental Glomerulosclerosis |
title_sort | case of podocytic infolding glomerulopathy with focal segmental glomerulosclerosis |
topic | Published online: August, 2013 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770251/ https://www.ncbi.nlm.nih.gov/pubmed/24027576 http://dx.doi.org/10.1159/000354591 |
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