[Solitary bone plasmacytoma: about 3 cases and review of the literature].

Autor:	Masmoudi K; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Elleuch E; Infectious diseases Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Akrout R; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Mnejja MA; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Feki A; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Ezzeddine M; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Baklouti S; Rhumatology Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia., Jemaâ B; Infectious diseases Department, Hédi Chaker University Hospital, El-Aïn Street Km 0,5 zip code 3029 Sfax, Tunisia.
Jazyk:	francouzština
Zdroj:	The Pan African medical journal [Pan Afr Med J] 2016 Dec 06; Vol. 25, pp. 219. Date of Electronic Publication: 2016 Dec 06 (Print Publication: 2016).
DOI:	10.11604/pamj.2016.25.219.10933
Abstrakt:	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. Competing Interests: Les auteurs ne déclarent aucun conflit d'intérêt.
Databáze:	MEDLINE
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