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Progress of diagnosis and treatment of acute mixed-cell leukemia / 白血病·淋巴瘤
Journal of Leukemia & Lymphoma ; (12): 634-636, 2017.
Article em Zh | WPRIM | ID: wpr-663000
Biblioteca responsável: WPRO
ABSTRACT
Acute mixed-cell leukemia (MPAL) is a rare high-risk leukemia that may originate from pluripotent hematopoietic stem cells.At present,the pathogenesis of MPAL is not clear,which mainly relys on immunophenotyping and molecular genetic diagnosis. Allogeneic hematopoietic stem cell transplantation may be the only way to cure the disease, depending on the immunophenotype and genetic characteristics of the leptin and/or myeloid induction chemotherapy. The prognosis of MPAL is worse than that of other acute leukemia, and understanding of these phenotypic genetic related clinical changes, biological significances and its pathogenesis will help to prevent and treat this disease effectively.
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Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: Zh Revista: Journal of Leukemia & Lymphoma Ano de publicação: 2017 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: Zh Revista: Journal of Leukemia & Lymphoma Ano de publicação: 2017 Tipo de documento: Article