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Progress in the treatment of disseminated intravascular coagulation in patients with acute promyelocytic leukemia / 国际儿科学杂志
Article em Zh | WPRIM | ID: wpr-751537
Biblioteca responsável: WPRO
ABSTRACT
Acute promyelocytic leukemia ( APL) is identified as the M3 subtype of acute myelo-cytic leukemia ( AML) . One of its clinical features is severe coagulation dysfunction. Most patients could de-velop disseminated intravascular coagulation ( DIC) resulting vital viscera hemorrhage, which is one of the significant causes of early death in APL patients. Early diagnosis and inductive therapy, dynamic monitoring pa-tients' coagulation index and correcting the abnormal coagulation could prevent the occurrence or progress of DIC, and then improving the early-term survival rate of APL patients. At present, APL is mainly treated from the treatment of primary disease, anticoagulant antifibrinolytic therapy, and alternative therapy.
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Texto completo: 1 Índice: WPRIM Tipo de estudo: Screening_studies Idioma: Zh Revista: International Journal of Pediatrics Ano de publicação: 2019 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Tipo de estudo: Screening_studies Idioma: Zh Revista: International Journal of Pediatrics Ano de publicação: 2019 Tipo de documento: Article