multicentric reticulohistiocytosis

mul·ti·cen·tric re·tic·u·lo·his·ti·o·cy·to·sis

a rare disease in which cutaneous papules composed of histiocytes containing glycolipids are associated with polyarthritis, often leading to shortening of the fingers.
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References in periodicals archive ?
Roentgenologic features of osteoarthritis, erosive osteoarthritis, ankylosing spondylitis, psoriatic arthritis, Reiter's disease, multicentric reticulohistiocytosis, and progressive systemic sclerosis.
Multicentric reticulohistiocytosis masquerading as lepromatous leprosy.
Multicentric reticulohistiocytosis is a rare systemic disease presenting with subcutaneous nodular lesions and symmetrical, erosive polyarthritis.
Multicentric reticulohistiocytosis with arthritis and cardiac infiltration: regression following treatment for underlying malignancy.
(7) Notable exceptions are solitary and multicentric reticulohistiocytosis, which are usually negative for factor XIIIa.
Immunohistochemical profile of multicentric reticulohistiocytosis [review].
Multicentric reticulohistiocytosis is a multi- system disorder which mainly involves the skin, joints and mucous membrane.
Histopathology helps to differentiate multicentric reticulohistiocytosis from eruptive xanthogranuloma and juvenile xanthogranulomas.
With the help of clinical findings, histopathological and immunocytochemical studies we confirmed the diagnosis of ulcerative multicentric reticulohistiocytosis. In the literature very few such cases have been reported.
Multicentric reticulohistiocytosis: systemic macrophage disorder.

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