Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review

Detalhes bibliográficos
Autor(a) principal: Serra, J
Data de Publicação: 2019
Outros Autores: Martinho, A, Duarte, F, Aldomiro, F
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.10/2327
Resumo: 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 Sarcoidosis and Multiple Myeloma: A Case Report and Literature ReviewSarcoidosisMultiple myelomaThe 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.HindawiRepositório do Hospital Prof. Doutor Fernando FonsecaSerra, JMartinho, ADuarte, FAldomiro, F2019-12-04T14:39:13Z2019-01-01T00:00:00Z2019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.10/2327engCase Rep Hematol. 2019;2019:45862652090-657910.1155/2019/4586265info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-20T15:53:01Zoai:repositorio.hff.min-saude.pt:10400.10/2327Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:53:16.546946Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
title Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
spellingShingle Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
Serra, J
Sarcoidosis
Multiple myeloma
title_short 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_sort Sarcoidosis and Multiple Myeloma: A Case Report and Literature Review
author Serra, J
author_facet Serra, J
Martinho, A
Duarte, F
Aldomiro, F
author_role author
author2 Martinho, A
Duarte, F
Aldomiro, F
author2_role author
author
author
dc.contributor.none.fl_str_mv Repositório do Hospital Prof. Doutor Fernando Fonseca
dc.contributor.author.fl_str_mv Serra, J
Martinho, A
Duarte, F
Aldomiro, F
dc.subject.por.fl_str_mv Sarcoidosis
Multiple myeloma
topic Sarcoidosis
Multiple myeloma
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.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-04T14:39:13Z
2019-01-01T00:00:00Z
2019-01-01T00:00:00Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.10/2327
url http://hdl.handle.net/10400.10/2327
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Case Rep Hematol. 2019;2019:4586265
2090-6579
10.1155/2019/4586265
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dc.publisher.none.fl_str_mv Hindawi
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