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Title: Histiocytic medullary reticulosis presenting as Mucha-Habermann disease. Author: Freeman MJ, Taylor JS, Levin HS, Dyment PG, Bergfeld WF. Journal: Acta Derm Venereol; 1978; 58(1):57-64. PubMed ID: 75636. Abstract: Histiocytic medullary reticulosis (HMR) is a rare, progressive, fatal reticuleondothelial proliferative disorder. It was diagnosed in a 10-year-old boy who had pityriasis lichenoides et varioliformis acuta of Mucha-Haberman which was controlled by dapsone for 2 years. One month after cessation of dapsone therapy, cutaneous tumors associated with fever, lymphadenopathy, and hepatosplenomegaly developed. Tissue biopsy specimens of skin, liver, spleen, lymph nodes, and a bone marrow aspirate demonstrated histiocytic erythrophagocytosis and atypical histiocytosis compatible with HMR. A rapidly progressing, fatal course followed despite intensive chemotherapy.[Abstract] [Full Text] [Related] [New Search]