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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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
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spelling doaj-a3330f7ad5114925a244282424fb33472020-11-24T23:12:17ZengWolters Kluwer Medknow PublicationsIndian Dermatology Online Journal2229-51782011-01-0122858710.4103/2229-5178.85998Multicentric reticulohistiocytosisSejal P ShahAditya M ShahSachin M PrajapatiFreny E BilimoriaMulticentric 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-year-old female was referred from Orthopedic Outpatient Department, with multiple, painful and tender nodules on the dorsum of her hands, forearms, elbows, back, and neck. The lesions were present predominantly around the joints with associated arthropathies. Smaller nodules were seen on the ear helices. There was no other clinically evident or investigative abnormality. A histopathological study confirmed the diagnosis of multicentric reticulohistiocytosis.http://www.idoj.in/article.asp?issn=2229-5178;year=2011;volume=2;issue=2;spage=85;epage=87;aulast=ShahArthritisgiant-cell reticulohistiocytosismulticentric reticulohistiocytosis
collection DOAJ
language English
format Article
sources DOAJ
author Sejal P Shah
Aditya M Shah
Sachin M Prajapati
Freny E Bilimoria
spellingShingle Sejal P Shah
Aditya M Shah
Sachin M Prajapati
Freny E Bilimoria
Multicentric reticulohistiocytosis
Indian Dermatology Online Journal
Arthritis
giant-cell reticulohistiocytosis
multicentric reticulohistiocytosis
author_facet Sejal P Shah
Aditya M Shah
Sachin M Prajapati
Freny E Bilimoria
author_sort Sejal P Shah
title Multicentric reticulohistiocytosis
title_short Multicentric reticulohistiocytosis
title_full Multicentric reticulohistiocytosis
title_fullStr Multicentric reticulohistiocytosis
title_full_unstemmed Multicentric reticulohistiocytosis
title_sort multicentric reticulohistiocytosis
publisher Wolters Kluwer Medknow Publications
series Indian Dermatology Online Journal
issn 2229-5178
publishDate 2011-01-01
description 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-year-old female was referred from Orthopedic Outpatient Department, with multiple, painful and tender nodules on the dorsum of her hands, forearms, elbows, back, and neck. The lesions were present predominantly around the joints with associated arthropathies. Smaller nodules were seen on the ear helices. There was no other clinically evident or investigative abnormality. A histopathological study confirmed the diagnosis of multicentric reticulohistiocytosis.
topic Arthritis
giant-cell reticulohistiocytosis
multicentric reticulohistiocytosis
url http://www.idoj.in/article.asp?issn=2229-5178;year=2011;volume=2;issue=2;spage=85;epage=87;aulast=Shah
work_keys_str_mv AT sejalpshah multicentricreticulohistiocytosis
AT adityamshah multicentricreticulohistiocytosis
AT sachinmprajapati multicentricreticulohistiocytosis
AT frenyebilimoria multicentricreticulohistiocytosis
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