Progress in the treatment of disseminated intravascular coagulation in patients with acute promyelocytic leukemia / 国际儿科学杂志
International Journal of Pediatrics
; (6): 674-677, 2019.
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.
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