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Podocytopathy in patients with monoclonal gammopathy: three patients and literature review
BACKGROUND: Renal manifestations of monoclonal gammopathies are of increasing interest among nephrologists. Typical manifestations include light chain cast nephropathy, amyloidosis or renal damage mediated by monoclonal immunoglobulin deposition. Podocytopathies in the setting of an underlying monoc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862048/ https://www.ncbi.nlm.nih.gov/pubmed/35211301 http://dx.doi.org/10.1093/ckj/sfab176 |
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author | Ribas, Andrés Puche, Adrián Gimeno, Javier Sans, Laia Barrios, Clara Márquez, Eva Naranjo, Dolores Lloveras, Belén Lop, Joan Ramos, Natàlia Soler, Maria José Gabaldon, Alejandra Crespo, Marta Rodríguez, Eva |
author_facet | Ribas, Andrés Puche, Adrián Gimeno, Javier Sans, Laia Barrios, Clara Márquez, Eva Naranjo, Dolores Lloveras, Belén Lop, Joan Ramos, Natàlia Soler, Maria José Gabaldon, Alejandra Crespo, Marta Rodríguez, Eva |
author_sort | Ribas, Andrés |
collection | PubMed |
description | BACKGROUND: Renal manifestations of monoclonal gammopathies are of increasing interest among nephrologists. Typical manifestations include light chain cast nephropathy, amyloidosis or renal damage mediated by monoclonal immunoglobulin deposition. Podocytopathies in the setting of an underlying monoclonal gammopathy constitute a rare manifestation of these diseases and, although being described in the literature, remain a challenge since most data derive from case reports. METHODS: A retrospective review of the clinical data of Hospital del Mar and Hospital Vall d’Hebron was performed to identify patients with minimal change disease (MCD) or focal and segmental glomerulosclerosis (FSGS) in the setting of neoplasms that produce monoclonal (M) protein. Additionally, a literature review on this topic was performed. This study aims to describe the clinical characteristics and outcomes of these patients. RESULTS: Three patients were identified to have podocytopathy and monoclonal gammopathy between the years 2013 and 2020. All three were males and >65 years of age. Two patients were diagnosed with MCD and one patient was diagnosed with FSGS. All patients underwent a kidney biopsy and light and electron microscopic studies were performed. The underlying causes of monoclonal gammopathy were multiple myeloma in two cases and Waldeström macroglobulinemia in one case. Two patients developed nephrotic syndrome during the follow-up. All patients were under active hematological treatment. One patient presented a complete remission of proteinuria whereas the other two presented a partial remission. CONCLUSIONS: Podocytopathies may infrequently be found in patients with monoclonal gammopathies. Patients with overt glomerular proteinuria and hematological disorders with M protein should undergo a kidney biopsy for prompt diagnosis and to specify a prognosis. In addition, further study on this matter must be done to understand the pathophysiology and treat these patients appropriately. |
format | Online Article Text |
id | pubmed-8862048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88620482022-02-23 Podocytopathy in patients with monoclonal gammopathy: three patients and literature review Ribas, Andrés Puche, Adrián Gimeno, Javier Sans, Laia Barrios, Clara Márquez, Eva Naranjo, Dolores Lloveras, Belén Lop, Joan Ramos, Natàlia Soler, Maria José Gabaldon, Alejandra Crespo, Marta Rodríguez, Eva Clin Kidney J CKJ Review BACKGROUND: Renal manifestations of monoclonal gammopathies are of increasing interest among nephrologists. Typical manifestations include light chain cast nephropathy, amyloidosis or renal damage mediated by monoclonal immunoglobulin deposition. Podocytopathies in the setting of an underlying monoclonal gammopathy constitute a rare manifestation of these diseases and, although being described in the literature, remain a challenge since most data derive from case reports. METHODS: A retrospective review of the clinical data of Hospital del Mar and Hospital Vall d’Hebron was performed to identify patients with minimal change disease (MCD) or focal and segmental glomerulosclerosis (FSGS) in the setting of neoplasms that produce monoclonal (M) protein. Additionally, a literature review on this topic was performed. This study aims to describe the clinical characteristics and outcomes of these patients. RESULTS: Three patients were identified to have podocytopathy and monoclonal gammopathy between the years 2013 and 2020. All three were males and >65 years of age. Two patients were diagnosed with MCD and one patient was diagnosed with FSGS. All patients underwent a kidney biopsy and light and electron microscopic studies were performed. The underlying causes of monoclonal gammopathy were multiple myeloma in two cases and Waldeström macroglobulinemia in one case. Two patients developed nephrotic syndrome during the follow-up. All patients were under active hematological treatment. One patient presented a complete remission of proteinuria whereas the other two presented a partial remission. CONCLUSIONS: Podocytopathies may infrequently be found in patients with monoclonal gammopathies. Patients with overt glomerular proteinuria and hematological disorders with M protein should undergo a kidney biopsy for prompt diagnosis and to specify a prognosis. In addition, further study on this matter must be done to understand the pathophysiology and treat these patients appropriately. Oxford University Press 2021-09-28 /pmc/articles/PMC8862048/ /pubmed/35211301 http://dx.doi.org/10.1093/ckj/sfab176 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the ERA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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 | CKJ Review Ribas, Andrés Puche, Adrián Gimeno, Javier Sans, Laia Barrios, Clara Márquez, Eva Naranjo, Dolores Lloveras, Belén Lop, Joan Ramos, Natàlia Soler, Maria José Gabaldon, Alejandra Crespo, Marta Rodríguez, Eva Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title | Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title_full | Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title_fullStr | Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title_full_unstemmed | Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title_short | Podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
title_sort | podocytopathy in patients with monoclonal gammopathy: three patients and literature review |
topic | CKJ Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862048/ https://www.ncbi.nlm.nih.gov/pubmed/35211301 http://dx.doi.org/10.1093/ckj/sfab176 |
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