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 (Author), Aditya M Shah (Author), Sachin M Prajapati (Author), Freny E Bilimoria (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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