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Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report
BACKGROUND: Membranous nephropathy (MN), the leading cause of nephrotic syndrome in adults, is characterized by the deposition of subepithelial immune deposits. Most of the cases are primary, while only approximately 25% of the cases are secondary to some known diseases. Recently, MN has been consid...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845168/ https://www.ncbi.nlm.nih.gov/pubmed/29523091 http://dx.doi.org/10.1186/s12882-018-0855-z |
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author | Mrabet, Sanda Aicha, Narjess Ben Abdessayed, Nihed Mokni, Moncef Achour, Abdellatif |
author_facet | Mrabet, Sanda Aicha, Narjess Ben Abdessayed, Nihed Mokni, Moncef Achour, Abdellatif |
author_sort | Mrabet, Sanda |
collection | PubMed |
description | BACKGROUND: Membranous nephropathy (MN), the leading cause of nephrotic syndrome in adults, is characterized by the deposition of subepithelial immune deposits. Most of the cases are primary, while only approximately 25% of the cases are secondary to some known diseases. Recently, MN has been considered to be a possible presentation of chronic graft-versus-host disease (GVHD) of the kidney in allogeneic hematopoietic stem cell transplantation (HSCT) patients. In autologous HSCT populations, there have been scarce reports of associated MN, as a result of immune dysregulation leading to systemic autoimmunity and miming chronic GVHD. CASE PRESENTATION: We report an exceptional case of MN associated to an acute renal failure occurring within days following an autologous HSCT indicated by multiple myeloma. There was no evidence of GVHD or myeloma relapse. A complete remission of nephrotic syndrome with normalization of renal function were rapidly obtained by corticosteroid therapy. CONCLUSION: This is the first published case of acute renal failure due to MN occurring in the acute phase of an autologous HSCT. These findings support the antibodymediated autoimmune glomerular disease. |
format | Online Article Text |
id | pubmed-5845168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58451682018-03-14 Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report Mrabet, Sanda Aicha, Narjess Ben Abdessayed, Nihed Mokni, Moncef Achour, Abdellatif BMC Nephrol Case Report BACKGROUND: Membranous nephropathy (MN), the leading cause of nephrotic syndrome in adults, is characterized by the deposition of subepithelial immune deposits. Most of the cases are primary, while only approximately 25% of the cases are secondary to some known diseases. Recently, MN has been considered to be a possible presentation of chronic graft-versus-host disease (GVHD) of the kidney in allogeneic hematopoietic stem cell transplantation (HSCT) patients. In autologous HSCT populations, there have been scarce reports of associated MN, as a result of immune dysregulation leading to systemic autoimmunity and miming chronic GVHD. CASE PRESENTATION: We report an exceptional case of MN associated to an acute renal failure occurring within days following an autologous HSCT indicated by multiple myeloma. There was no evidence of GVHD or myeloma relapse. A complete remission of nephrotic syndrome with normalization of renal function were rapidly obtained by corticosteroid therapy. CONCLUSION: This is the first published case of acute renal failure due to MN occurring in the acute phase of an autologous HSCT. These findings support the antibodymediated autoimmune glomerular disease. BioMed Central 2018-03-09 /pmc/articles/PMC5845168/ /pubmed/29523091 http://dx.doi.org/10.1186/s12882-018-0855-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Mrabet, Sanda Aicha, Narjess Ben Abdessayed, Nihed Mokni, Moncef Achour, Abdellatif Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title | Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title_full | Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title_fullStr | Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title_full_unstemmed | Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title_short | Membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
title_sort | membranous nephropathy succeeding autologous hematopoietic stem cell transplant: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845168/ https://www.ncbi.nlm.nih.gov/pubmed/29523091 http://dx.doi.org/10.1186/s12882-018-0855-z |
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