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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Bibliographic Details
Main Authors: Sejal P Shah, Aditya M Shah, Sachin M Prajapati, Freny E Bilimoria
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2011-01-01
Series:Indian Dermatology Online Journal
Subjects:
Online Access:http://www.idoj.in/article.asp?issn=2229-5178;year=2011;volume=2;issue=2;spage=85;epage=87;aulast=Shah