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Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review

The existence of a sarcoidosis-lymphoma syndrome has been previously proposed since the relation between sarcoidosis and an increased risk of lymphoproliferative disorders is well established. Multiple myeloma is a malignant multifocal proliferation of clonal plasma cells within the bone marrow, and...

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Autores principales: Tiago Serra, Joao, Martinho, Aurelia, Paixao Duarte, Fernanda, Aldomiro, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875373/
https://www.ncbi.nlm.nih.gov/pubmed/31781424
http://dx.doi.org/10.1155/2019/4586265
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author Tiago Serra, Joao
Martinho, Aurelia
Paixao Duarte, Fernanda
Aldomiro, Fernando
author_facet Tiago Serra, Joao
Martinho, Aurelia
Paixao Duarte, Fernanda
Aldomiro, Fernando
author_sort Tiago Serra, Joao
collection PubMed
description The existence of a sarcoidosis-lymphoma syndrome has been previously proposed since the relation between sarcoidosis and an increased risk of lymphoproliferative disorders is well established. Multiple myeloma is a malignant multifocal proliferation of clonal plasma cells within the bone marrow, and its association with sarcoidosis has been rarely described. We present a concurrent diagnosis of sarcoidosis and multiple myeloma and make a brief analysis of the reported cases in the literature. A 65-year-old woman underwent surgery for the excision of a wrist mass that presented 3 years before. Histological analysis showed sarcoid-type epithelioid granulomas without necrosis, establishing soft tissue sarcoidosis. Further evaluation revealed marked interstitial lung parenchyma lesions and large intrathoracic adenopathies. Bronchofibroscopy with transbronchial biopsy confirmed lung sarcoidosis. In addition, blood analysis showed monoclonal IgG kappa gammopathy. A bone marrow biopsy confirmed hypercellularity with 60% plasma cells and plasmocyte infiltration. Thus, the diagnosis of systemic sarcoidosis and multiple myeloma was established simultaneously. In a brief review of the literature, we identified 33 reports of cases with both sarcoidosis and multiple myeloma. We point out the importance of a high level of suspicion for the association of sarcoidosis with malignant haematological diseases such as multiple myeloma.
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spelling pubmed-68753732019-11-28 Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review Tiago Serra, Joao Martinho, Aurelia Paixao Duarte, Fernanda Aldomiro, Fernando Case Rep Hematol Case Report The existence of a sarcoidosis-lymphoma syndrome has been previously proposed since the relation between sarcoidosis and an increased risk of lymphoproliferative disorders is well established. Multiple myeloma is a malignant multifocal proliferation of clonal plasma cells within the bone marrow, and its association with sarcoidosis has been rarely described. We present a concurrent diagnosis of sarcoidosis and multiple myeloma and make a brief analysis of the reported cases in the literature. A 65-year-old woman underwent surgery for the excision of a wrist mass that presented 3 years before. Histological analysis showed sarcoid-type epithelioid granulomas without necrosis, establishing soft tissue sarcoidosis. Further evaluation revealed marked interstitial lung parenchyma lesions and large intrathoracic adenopathies. Bronchofibroscopy with transbronchial biopsy confirmed lung sarcoidosis. In addition, blood analysis showed monoclonal IgG kappa gammopathy. A bone marrow biopsy confirmed hypercellularity with 60% plasma cells and plasmocyte infiltration. Thus, the diagnosis of systemic sarcoidosis and multiple myeloma was established simultaneously. In a brief review of the literature, we identified 33 reports of cases with both sarcoidosis and multiple myeloma. We point out the importance of a high level of suspicion for the association of sarcoidosis with malignant haematological diseases such as multiple myeloma. Hindawi 2019-10-30 /pmc/articles/PMC6875373/ /pubmed/31781424 http://dx.doi.org/10.1155/2019/4586265 Text en Copyright © 2019 Joao Tiago Serra et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tiago Serra, Joao
Martinho, Aurelia
Paixao Duarte, Fernanda
Aldomiro, Fernando
Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title_full Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title_fullStr Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title_full_unstemmed Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title_short Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title_sort sarcoidosis and multiple myeloma: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875373/
https://www.ncbi.nlm.nih.gov/pubmed/31781424
http://dx.doi.org/10.1155/2019/4586265
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