Cutaneous involvement in malignant histiocytosis. Case report and review of the literature
- 1 May 1981
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Dermatology
- Vol. 117 (5) , 278-281
- https://doi.org/10.1001/archderm.117.5.278
Abstract
Malignant histiocytosis (MH) is a rare, malignant neoplasm with protein manifestations, including fever, lymphadenopathy, hepatosplenomegaly, pancytopenia and, infrequently, cutaneous lesions. A patient had initial manifestations that included fever and skin lesions. Skin lesions began on distal areas of the extremities and spread to involve proximal areas of the extremities and the abdomen. Erythematous maculopapular lesions, nodules and plaques were present in various stages of development, which evolved into ulcerated plaques that exuded a serosanguineous discharge. Spontaneous healing of lesions occurred, leaving hyperpigmented, atrophic scars. Histologically, the deep dermis and subcutaneous tissues contained a diffuse infiltrate of histiocytes, lymphocytes and mononuclear cells. Erythrophagocytosis by histiocytes was present in the skin biopsy material; 13% of 320 cases in the literature had skin involvement. Based on this report and review of the literature, in selected cases, skin biopsy may contribute to the diagnosis of MH.This publication has 5 references indexed in Scilit:
- Malignant Histiocytosis: A Clinico‐pathological Study of 12 CasesBritish Journal of Haematology, 1978
- Malignant Histiocytosis: A Clinicopathologic Study of 18 Consecutive CasesTumori Journal, 1978
- Histiocytic medullary reticulosis presenting as Mucha-Habermann diseaseActa Dermato-Venereologica, 1978
- Chemotherapy of malignant histiocytosis in adultsCancer, 1977
- Necropsy and ultrastructural findings in histiocytic medullary reticulosisBritish Journal of Dermatology, 1976