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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications Pvt Ltd
2011
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| Matèries: | |
| Accés en línia: | 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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