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  • Title: [Multicentric reticulo-histiocytosis; review of recent literature (since 1969)].
    Author: Chevrant-Breton J.
    Journal: Ann Dermatol Venereol; 1977 Nov; 104(11):745-53. PubMed ID: 206176.
    Abstract:
    The review of recent literature (since 1969) shows 35 cases of multicentric reticulo-histiocytosis. This entity was first described as a dermatological disease, then as a dermatoarthritis. It is in fact a systemic disease which can involve many organs but is sometimes monosymptomatic. Its fatal outcome is, sometimes, the result of a disseminated neoplasia or a lymphoma. Its clinical and microscopic features allow to distinguish it from solitary reticulo-histiocytoma, generalized eruptive histiocytoma, congenital reticulo-histiocytosis of Hashimoto and Pritzker and familial histiocytic dermato-arthritis of Zayid.
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