作者: MS Tallman , HC Kwaan
DOI: 10.1182/BLOOD.V79.3.543.543
关键词:
摘要: of the prothrombin (PT), activated partial thromboplastin (PTT) and thrombin times (TT), increased levels fibrin degradation products (FDPs), hypofibrin~genemia.~~~"~~~~~ These findings are not diagnostic any single coagulation disorder, but reflect a complex interaction several pathophysiologic processes depicted in Fig 1. The first most generally recognized abnormality is release procoagulants from APL cells resulting DIC. Several types procoagulant activity have been found capable activating factor X through both intrinsic extrinsic pathways, including tissue factorlike