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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...

詳細記述

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書誌詳細
主要な著者: Shah, Sejal P., Shah, Aditya M., Prajapati, Sachin M., Bilimoria, Freny E.
フォーマット: Artigo
言語:Inglês
出版事項: Medknow Publications Pvt Ltd 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3481828/
https://ncbi.nlm.nih.gov/pubmed/23130232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.85998
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