Tatewaki W
First department of Internal medicine, Niigata University School of Medicine.
Nihon Rinsho. 1993 Jan;51(1):146-50.
Thrombotic thrombocytopenic purpura (TTP) is an uncommon disorder. Several hypotheses have been reported up to now but, the pathogenesis is not yet clear. On the other hand, von Willebrand factor (vWf) plays a role in platelet agglutination in initial hemostasis. Moake and other investigators suggested plasma vWf abnormalities. In this paper, we analysed vWf antigen, ristocetin cofactor (RCof) and multimeric composition of vWf in 16 patients with TTP. It was found that vWf antigen and RCof ranged from very low to very high levels, but RCof was lower than vWf antigen except in two cases. Decrease of large multimer of vWf was seen in 11 patients (69%). These abnormalities were corrected at remission by therapy.
血栓性血小板减少性紫癜(TTP)是一种罕见的疾病。迄今为止,已有多种假说被报道,但发病机制仍不清楚。另一方面,血管性血友病因子(vWf)在初始止血过程中血小板凝集方面发挥作用。莫克及其他研究者提出血浆vWf异常。在本文中,我们分析了16例TTP患者的vWf抗原、瑞斯托霉素辅因子(RCof)以及vWf的多聚体组成。结果发现,vWf抗原和RCof水平从极低到极高不等,但除两例外,RCof低于vWf抗原。11例患者(69%)出现vWf大分子多聚体减少。这些异常在治疗缓解时得到纠正。