Kahle L H, Avvisati G, Lamping R J, Moretti T, Mandelli F, ten Cate J W
Scand J Clin Lab Invest Suppl. 1985;178:75-80.
Patients with acute promyelocytic leukemia have a bleeding disorder which was thus far explained by a coagulopathy based on diffuse intravascular coagulation (DIC). We observed severe alpha-2-antiplasmin deficiency in a consecutive series of such patients. We postulate proteolysis rather than DIC, also because of increased turnover of 125I-alpha-2-antiplasmin, to be responsible for the coagulopathy. Alpha-2-antiplasmin deficiency may well contribute to the bleeding disorder in acute promyelocytic leukemia.
急性早幼粒细胞白血病患者存在出血性疾病,迄今为止,这种疾病被认为是由基于弥散性血管内凝血(DIC)的凝血病所导致。我们在一系列此类连续患者中观察到严重的α2抗纤溶酶缺乏。我们推测蛋白水解而非DIC是导致凝血病的原因,这也是由于125I-α2抗纤溶酶的周转率增加所致。α2抗纤溶酶缺乏很可能是急性早幼粒细胞白血病出血性疾病的一个促成因素。