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- W2318402415 abstract "Four patients, aged 46, 61, 22, and 73 years, were studied for their fatal disease characterized by fever, cutaneous infiltrate, pruritus, generalized lymphadenopathy, hepatosplenomegaly, and eosinophilia. Pathologically, there was a systemic proliferation of non-phagocytic immature histiocytes in various organs in every patient. Their clinical courses lasted 7, 21, 36, and 6 months, respectively. Their disease process shared certain clinical and pathologic features with malignant histiocytosis, reported as histiocytic medullary reticulosis, and leukemic reticuloendotheliosis, and partly with histiocytosis X. It is best classified as a variant of malignant histiocytosis." @default.
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- W2318402415 date "1972-04-01" @default.
- W2318402415 modified "2023-09-23" @default.
- W2318402415 title "Malignant Histiocytosis with Cutaneous Involvement and Eosinophilia" @default.
- W2318402415 doi "https://doi.org/10.1093/ajcp/57.4.438" @default.
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