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Hematological entities with plasmacytic differentiation: a case report 

INTRODUCTION: Plasmacytoma, a localized tumor of monoclonal plasma cells without any clinical, radiological or physical evidence of plasma cell neoplasm (PCN), is a rare entity that accounts for 1% of PCN. Immunoglobulin M (IgM) extramedullary plasmacytoma of mediastinal region has never been report...

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Autores principales: Inamdar, Arati, Bhattacharyya, Siddharth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521441/
https://www.ncbi.nlm.nih.gov/pubmed/37749639
http://dx.doi.org/10.1186/s13256-023-04082-x
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author Inamdar, Arati
Bhattacharyya, Siddharth
author_facet Inamdar, Arati
Bhattacharyya, Siddharth
author_sort Inamdar, Arati
collection PubMed
description INTRODUCTION: Plasmacytoma, a localized tumor of monoclonal plasma cells without any clinical, radiological or physical evidence of plasma cell neoplasm (PCN), is a rare entity that accounts for 1% of PCN. Immunoglobulin M (IgM) extramedullary plasmacytoma of mediastinal region has never been reported and is a diagnostic challenge considering other differential diagnoses. CASE PRESENTATION: We present the case of a 51-year-old African-American female with progressively increasing cough, dyspnea, and dysphagia for 6 months with a computed tomography (CT) scan revealing a subcarinal mass. The histopathological analysis of the mass reveals a diagnosis of lymphoma with plasma cell differentiation, with a differential of lymphoplasmacytic lymphoma and plasma cell neoplasm. The lymphoma panel via next-generation sequencing (NGS) and a myeloma-targeted fluorescent in situ hybridization (FISH) panel confirmed the diagnosis of IgM extramedullary plasmacytoma, an entity of rare occurrence. Treatment with radiation led to complete regression of the plasmacytoma with normal blood work-up. CONCLUSIONS: This report describes the challenges of diagnosing IgM extramedullary plasmactyoma. Our case report highlights the importance of cytogenetics and NGS in establishing a correct diagnosis that indeed has prognostic and therapeutic implications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13256-023-04082-x.
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spelling pubmed-105214412023-09-27 Hematological entities with plasmacytic differentiation: a case report  Inamdar, Arati Bhattacharyya, Siddharth J Med Case Rep Case Report INTRODUCTION: Plasmacytoma, a localized tumor of monoclonal plasma cells without any clinical, radiological or physical evidence of plasma cell neoplasm (PCN), is a rare entity that accounts for 1% of PCN. Immunoglobulin M (IgM) extramedullary plasmacytoma of mediastinal region has never been reported and is a diagnostic challenge considering other differential diagnoses. CASE PRESENTATION: We present the case of a 51-year-old African-American female with progressively increasing cough, dyspnea, and dysphagia for 6 months with a computed tomography (CT) scan revealing a subcarinal mass. The histopathological analysis of the mass reveals a diagnosis of lymphoma with plasma cell differentiation, with a differential of lymphoplasmacytic lymphoma and plasma cell neoplasm. The lymphoma panel via next-generation sequencing (NGS) and a myeloma-targeted fluorescent in situ hybridization (FISH) panel confirmed the diagnosis of IgM extramedullary plasmacytoma, an entity of rare occurrence. Treatment with radiation led to complete regression of the plasmacytoma with normal blood work-up. CONCLUSIONS: This report describes the challenges of diagnosing IgM extramedullary plasmactyoma. Our case report highlights the importance of cytogenetics and NGS in establishing a correct diagnosis that indeed has prognostic and therapeutic implications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13256-023-04082-x. BioMed Central 2023-09-26 /pmc/articles/PMC10521441/ /pubmed/37749639 http://dx.doi.org/10.1186/s13256-023-04082-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Inamdar, Arati
Bhattacharyya, Siddharth
Hematological entities with plasmacytic differentiation: a case report 
title Hematological entities with plasmacytic differentiation: a case report 
title_full Hematological entities with plasmacytic differentiation: a case report 
title_fullStr Hematological entities with plasmacytic differentiation: a case report 
title_full_unstemmed Hematological entities with plasmacytic differentiation: a case report 
title_short Hematological entities with plasmacytic differentiation: a case report 
title_sort hematological entities with plasmacytic differentiation: a case report 
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521441/
https://www.ncbi.nlm.nih.gov/pubmed/37749639
http://dx.doi.org/10.1186/s13256-023-04082-x
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