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A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood
BACKGROUND: Common variable immunodeficiency (CVID) is a disorder characterized by hypogammaglobulinemia without a known predisposing cause. CASE PRESENTATION: We report a 36-year-old man who had suffered membranoproliferative glomerulonephritis (MPGN) in his childhood, later diagnosed with CVID at...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462670/ https://www.ncbi.nlm.nih.gov/pubmed/22727088 http://dx.doi.org/10.1186/1471-2369-13-46 |
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author | Tsuji, Kenji Uchida, Haruhito Adam Ono, Tetsuichirou Inoue, Tatsuyuki Shinagawa, Katsuji Kitamura, Shinji Maeshima, Yohei Sugiyama, Hitoshi Makino, Hirofumi |
author_facet | Tsuji, Kenji Uchida, Haruhito Adam Ono, Tetsuichirou Inoue, Tatsuyuki Shinagawa, Katsuji Kitamura, Shinji Maeshima, Yohei Sugiyama, Hitoshi Makino, Hirofumi |
author_sort | Tsuji, Kenji |
collection | PubMed |
description | BACKGROUND: Common variable immunodeficiency (CVID) is a disorder characterized by hypogammaglobulinemia without a known predisposing cause. CASE PRESENTATION: We report a 36-year-old man who had suffered membranoproliferative glomerulonephritis (MPGN) in his childhood, later diagnosed with CVID at 35 years of age. He presented at our hospital with signs of proteinuria. A renal biopsy revealed he suffered from focal segmental glomerulosclerosis (FSGS), possibly due to obesity and hypertension, not CVID - associated MPGN. CONCLUSION: This is the first case report of FSGS in a CVID patient. In this case, we have to pay attention not only to the treatment of obesity and hypertension for FSGS but also to the recurrence of immune-complex glomerulonephritis such as MPGN, in case of the restoration of hypogammaglobulinemia. |
format | Online Article Text |
id | pubmed-3462670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34626702012-10-03 A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood Tsuji, Kenji Uchida, Haruhito Adam Ono, Tetsuichirou Inoue, Tatsuyuki Shinagawa, Katsuji Kitamura, Shinji Maeshima, Yohei Sugiyama, Hitoshi Makino, Hirofumi BMC Nephrol Case Report BACKGROUND: Common variable immunodeficiency (CVID) is a disorder characterized by hypogammaglobulinemia without a known predisposing cause. CASE PRESENTATION: We report a 36-year-old man who had suffered membranoproliferative glomerulonephritis (MPGN) in his childhood, later diagnosed with CVID at 35 years of age. He presented at our hospital with signs of proteinuria. A renal biopsy revealed he suffered from focal segmental glomerulosclerosis (FSGS), possibly due to obesity and hypertension, not CVID - associated MPGN. CONCLUSION: This is the first case report of FSGS in a CVID patient. In this case, we have to pay attention not only to the treatment of obesity and hypertension for FSGS but also to the recurrence of immune-complex glomerulonephritis such as MPGN, in case of the restoration of hypogammaglobulinemia. BioMed Central 2012-06-24 /pmc/articles/PMC3462670/ /pubmed/22727088 http://dx.doi.org/10.1186/1471-2369-13-46 Text en Copyright ©2012 Tsuji et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Tsuji, Kenji Uchida, Haruhito Adam Ono, Tetsuichirou Inoue, Tatsuyuki Shinagawa, Katsuji Kitamura, Shinji Maeshima, Yohei Sugiyama, Hitoshi Makino, Hirofumi A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title | A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title_full | A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title_fullStr | A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title_full_unstemmed | A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title_short | A case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
title_sort | case of focal segmental glomerulosclerosis in an adult patient with hypogammaglobulinemia superimposed on membranoproliferative glomerulonephritis in childhood |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462670/ https://www.ncbi.nlm.nih.gov/pubmed/22727088 http://dx.doi.org/10.1186/1471-2369-13-46 |
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