Helmchen C, Nahser H C, Yousry T, Witt T N, Kühne D
Neurologische Klinik, Klinikum Grosshadern, Ludwig-Maximilians-Universität München.
Nervenarzt. 1995 Feb;66(2):124-8.
Little is known about the course of cerebral aneurysms in hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber's disease). Thus, therapeutic decisions are often difficult. For the first time, we report the successful embolization of an arteriovenous fistula and multiple aneurysms of the posterior inferior cerebellar artery (PICA) of a patient with Rendu-Osler-Weber's disease after subarachnoid hemorrhage. Two years later she suffered another severe intracranial hemorrhage. Angiography revealed an aneurysm in the same artery (PICA), which spontaneously disappeared within 2 months. Spontaneous regression of aneurysms in Rendu-Osler-Weber's disease has not been reported before.
关于遗传性出血性毛细血管扩张症(朗杜-奥斯勒-韦伯病)中脑动脉瘤的病程,人们了解甚少。因此,治疗决策往往很困难。我们首次报告了1例患有朗杜-奥斯勒-韦伯病的患者在蛛网膜下腔出血后,其小脑后下动脉(PICA)动静脉瘘和多发动脉瘤成功栓塞的病例。两年后,她再次发生严重的颅内出血。血管造影显示同一动脉(PICA)有一个动脉瘤,该动脉瘤在2个月内自行消失。此前尚未有关于朗杜-奥斯勒-韦伯病中动脉瘤自发消退的报道。