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[血栓性血小板减少性紫癜病程中血管性血友病因子多聚体的变化]

[The changes in von Willebrand factor multimer in a course of thrombotic thrombocytopenic purpura].

作者信息

Saitoh M, Wada H, Tanigawa M, Tamaki S, Masuya M, Minami N, Deguchi K, Shirakawa S, Tatewaki W, Takahashi H

机构信息

2nd Department of Internal Medicine, Mie University School of Medicine.

出版信息

Rinsho Ketsueki. 1991 Sep;32(9):1006-8.

PMID:1942536
Abstract

A 51 year-old woman with severe thrombocytopenia, hemolytic anemia, renal failure and loss of consciousness, and significant decrease in plasma large multimer of von Willebrand Factor (vWF) was diagnosed as having thrombotic thrombocytopenic purpura (TTP). She was treated with plasma exchange, anti-platelet agents and steroids. Although she showed temporary improvement and return of vWF multimer to a normal level, her symptoms reappeared, vWF large multimer level showed a remarkable increase, and she died because of pulmonary bleeding. It would be important that the vWF multimer bands changed in the course of TTP.

摘要

一名51岁女性,患有严重血小板减少症、溶血性贫血、肾衰竭和意识丧失,血浆中血管性血友病因子(vWF)的大型多聚体显著减少,被诊断为血栓性血小板减少性紫癜(TTP)。她接受了血浆置换、抗血小板药物和类固醇治疗。尽管她出现了暂时改善,vWF多聚体水平恢复到正常水平,但症状再次出现,vWF大型多聚体水平显著升高,她最终因肺出血死亡。TTP病程中vWF多聚体条带发生变化这一点很重要。

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