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Oral medullary plasmacytoma: Rare case reports

Medullary plasmacytoma (MP) or osseous or solitary bone plasmacytoma is a specializing hematopathology lesion typically present with local symptoms, such as pain, paresthesia and pathologic bone fractures as a result of proliferation of plasma cells. The most often involved sites are active hematopo...

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Detalles Bibliográficos
Autores principales: Narasimhan, Malathi, Chinnaswamy, Ravindran, V Giri, G V, Subramani, Vijaya Nirmala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069149/
https://www.ncbi.nlm.nih.gov/pubmed/32189906
http://dx.doi.org/10.4103/jomfp.JOMFP_37_19
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author Narasimhan, Malathi
Chinnaswamy, Ravindran
V Giri, G V
Subramani, Vijaya Nirmala
author_facet Narasimhan, Malathi
Chinnaswamy, Ravindran
V Giri, G V
Subramani, Vijaya Nirmala
author_sort Narasimhan, Malathi
collection PubMed
description Medullary plasmacytoma (MP) or osseous or solitary bone plasmacytoma is a specializing hematopathology lesion typically present with local symptoms, such as pain, paresthesia and pathologic bone fractures as a result of proliferation of plasma cells. The most often involved sites are active hematopoietic long bones and the vertebrae. The clinical course of disease is identical to spectrum of other plasma cell dyscrasias. The diagnostic criteria include punched-out radiolucencies, monoclonal plasma cells and M protein. This lesion should be considered for the differential diagnosis of bone tumors. It is highly radiosensitive although combination modalities of radiation, surgery and chemotherapy have been used in the treatment. The long-term follow-up is essential. We report two rare cases of oral MP with unusual clinical presentation.
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spelling pubmed-70691492020-03-18 Oral medullary plasmacytoma: Rare case reports Narasimhan, Malathi Chinnaswamy, Ravindran V Giri, G V Subramani, Vijaya Nirmala J Oral Maxillofac Pathol Case Report Medullary plasmacytoma (MP) or osseous or solitary bone plasmacytoma is a specializing hematopathology lesion typically present with local symptoms, such as pain, paresthesia and pathologic bone fractures as a result of proliferation of plasma cells. The most often involved sites are active hematopoietic long bones and the vertebrae. The clinical course of disease is identical to spectrum of other plasma cell dyscrasias. The diagnostic criteria include punched-out radiolucencies, monoclonal plasma cells and M protein. This lesion should be considered for the differential diagnosis of bone tumors. It is highly radiosensitive although combination modalities of radiation, surgery and chemotherapy have been used in the treatment. The long-term follow-up is essential. We report two rare cases of oral MP with unusual clinical presentation. Wolters Kluwer - Medknow 2020-02 2020-02-28 /pmc/articles/PMC7069149/ /pubmed/32189906 http://dx.doi.org/10.4103/jomfp.JOMFP_37_19 Text en Copyright: © 2020 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Narasimhan, Malathi
Chinnaswamy, Ravindran
V Giri, G V
Subramani, Vijaya Nirmala
Oral medullary plasmacytoma: Rare case reports
title Oral medullary plasmacytoma: Rare case reports
title_full Oral medullary plasmacytoma: Rare case reports
title_fullStr Oral medullary plasmacytoma: Rare case reports
title_full_unstemmed Oral medullary plasmacytoma: Rare case reports
title_short Oral medullary plasmacytoma: Rare case reports
title_sort oral medullary plasmacytoma: rare case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069149/
https://www.ncbi.nlm.nih.gov/pubmed/32189906
http://dx.doi.org/10.4103/jomfp.JOMFP_37_19
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