Leucemia prolinfocítica T variante de células cerebriformes. Presentación de un caso y revisión de la literatura
Author
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Peña, Camila
Author
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Valladares, Ximena
Author
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Soto, Carolina
Author
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Encina, Andrea
Author
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Marinov Martinic, Neda
Author
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Undurraga, Maria Soledad
Author
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Cabrera, Maria Elena
Admission date
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2016-06-24T15:43:04Z
Available date
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2016-06-24T15:43:04Z
Publication date
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2016
Cita de ítem
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Rev. Med. Chile 2016; 144: 124-128
en_US
Identifier
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https://repositorio.uchile.cl/handle/2250/139118
General note
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Artículo de publicación ISI
en_US
Abstract
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T cell Prolymphocytic Leukemia (T-PLL) is a rare and aggressive mature T cell Lymphocyte Leukemia. Twenty five percent of cases present as a small cell variant, and only 5% as a cerebriform variant. We report a 58 year-old man with rapidly progressive severe leukocytosis, skin lesions, lymphadenopathy, hepatosplenomegaly and pleural effusion. The lymphocytes had a cerebriform type. The diagnosis of T-PLL variant was made by morphology and immunophenotype study of peripheral blood. Karyotype was found to be complex. He was refractory to chemotherapy and died two months later.