Murphy W G, Moore J C, Warkentin T E, Hayward C P, Kelton J G
McMaster University Medical Centre, Hamilton, Ontario, Canada.
Blood Coagul Fibrinolysis. 1992 Oct;3(5):655-9. doi: 10.1097/00001721-199210000-00023.
Thrombotic thrombocytopenic purpura is an uncommon disorder, but it continues to be of considerable interest. The disease mechanisms are unclear and the aetiology is unknown. Perhaps most enigmatic of all, the mode of action of plasma therapy, which successfully induces remission in about two-thirds of cases, is wholly inexplicable. There are currently several areas of debate on the subject of thrombotic thrombocytopenic purpura. This paper addresses these points of contention: the definition of the disease, its distinction from haemolytic uraemic syndrome, the nature of the platelet aggregating factors in the plasma of patients with acute disease, the importance of the abnormalities of von Willebrand's factor observed in the acute and quiescent phases of the disease, the nature of the factor in normal plasma that induces remission, and the possible causes of the observed superiority of plasma exchange combined with plasma infusion, over plasma infusion alone.
血栓性血小板减少性紫癜是一种罕见的疾病,但它仍然备受关注。其发病机制尚不清楚,病因也不明。也许最令人费解的是,血浆疗法能使约三分之二的病例成功缓解,但其作用方式却完全无法解释。目前关于血栓性血小板减少性紫癜这一主题存在几个争议领域。本文讨论了以下争论点:该疾病的定义、它与溶血性尿毒症综合征的区别、急性病患者血浆中血小板聚集因子的性质、在疾病急性期和缓解期观察到的血管性血友病因子异常的重要性、正常血浆中诱导缓解的因子的性质,以及观察到的血浆置换联合血浆输注优于单纯血浆输注的可能原因。