Friederich P W, Wever P C, Briët E, Doorenbos C J, Levi M
Department of Vascular Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Am J Hematol. 2001 Apr;66(4):292-4. doi: 10.1002/ajh.1060.
We describe an elderly man who presented with life-threatening hematuria and gastrointestinal bleeding caused by acquired von Willebrand disease associated with monoclonal gammopathy of undetermined significance (MGUS). Standard therapy with desmopressin, von Willebrand factor-containing factor VIII concentrate, tranexamic acid, and immunoglobulin failed to achieve adequate hemostasis. However, treatment with recombinant activated factor VII (rFVIIa) arrested the bleeding completely. Since acquired von Willebrand disease can lead to life-threatening hemorrhage, clinicians should consider rFVIIa as an effective treatment option if standard therapy fails.
我们描述了一名老年男性,他因意义未明的单克隆丙种球蛋白病(MGUS)相关的获得性血管性血友病而出现危及生命的血尿和胃肠道出血。去氨加压素、含血管性血友病因子的凝血因子 VIII 浓缩物、氨甲环酸和免疫球蛋白的标准治疗未能实现充分止血。然而,重组活化因子 VII(rFVIIa)治疗使出血完全停止。由于获得性血管性血友病可导致危及生命的出血,如果标准治疗失败,临床医生应考虑将 rFVIIa 作为一种有效的治疗选择。