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- W2463286196 abstract "We describe the case of a 17-year-old Hispanic boy who had had erythroderma and diffuse lymphadenopathy for approximately 6 months. A diagnosis of Sézary syndrome was made on the basis of the histologic features of the skin; the presence of the same T-cell clone on the skin, blood, and bone marrow; and the high CD4(+) lymphocyte count with an aberrant phenotype in peripheral blood; bone marrow involvement was also present. The patient was treated with systemic gemcitabine and achieved partial remission." @default.
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- W2463286196 date "2016-07-11" @default.
- W2463286196 modified "2023-10-15" @default.
- W2463286196 title "Sézary Syndrome in a 17-Year-Old Boy: Clinicopathologic Features and Genomic Profile" @default.
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- W2463286196 doi "https://doi.org/10.1111/pde.12930" @default.
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