Le plasmocytome solitaire osseux: à propos de 3 cas et revue de la littérature

Solitary plasmocytomas are rare, accounting for less than 5% of all plasmocytes proliferations. Its diagnosis is based on the presence of localized tumor of monoclonal plasma cells cytologically identical to those of multiple myeloma, in the absence of other signs of a disseminated form. This study...

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Detalles Bibliográficos
Autores principales: Masmoudi, Karim, Elleuch, Emna, Akrout, Rim, Mnejja, Mohamed Amine, Feki, Afef, Ezzeddine, Mariam, Baklouti, Sofiène, Jemaâ, Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326196/
https://www.ncbi.nlm.nih.gov/pubmed/28292172
http://dx.doi.org/10.11604/pamj.2016.25.219.10933
Descripción
Sumario:Solitary plasmocytomas are rare, accounting for less than 5% of all plasmocytes proliferations. Its diagnosis is based on the presence of localized tumor of monoclonal plasma cells cytologically identical to those of multiple myeloma, in the absence of other signs of a disseminated form. This study aims to carry out a retrospective study of three cases of solitary bone plasmocytomas associated with a detailed review of the literature describing the diagnostic, therapeutic and evolving characteristics of this rare entity.

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