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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...

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Bibliographic Details
Main Authors: Shah, Sejal P., Shah, Aditya M., Prajapati, Sachin M., Bilimoria, Freny E.
Format: Artigo
Language:Inglês
Published: Medknow Publications Pvt Ltd 2011
Subjects:
Online Access: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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