Multicentric reticulohistiocytosis

Multicentric reticulohistiocytosis is a rare systemic granulomatous disease of an unknown cause, characterized by distinct histopathology. The skin, mucosa, synovial, bone, and internal organs may be involved. Cutaneous nodules and distinctive arthritis are the most prominent clinical features. A 55...

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Detalhes bibliográficos
Main Authors: Sejal P Shah, Aditya M Shah, Sachin M Prajapati, Freny E Bilimoria
Formato: Artigo
Idioma:English
Publicado em: Wolters Kluwer Medknow Publications 2011-01-01
Colecção:Indian Dermatology Online Journal
Assuntos:
Acesso em linha:http://www.idoj.in/article.asp?issn=2229-5178;year=2011;volume=2;issue=2;spage=85;epage=87;aulast=Shah