Aesch B, Lioret E, de Toffol B, Jan M
Department of Neurosciences, Centre Hospitalier Universitaire Bretonneau, Tours, France.
Neurosurgery. 1991 Oct;29(4):599-602. doi: 10.1097/00006123-199110000-00020.
A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous telangiectases. Review of the literature shows that in 12 previously published cases involving multiple arteriovenous malformations, this diagnosis was established five times. The indications for surgical treatment are discussed.
一名25岁男性在发生蛛网膜下腔出血后住院。血管造影显示有两个动静脉畸形，其中一个无症状。由于同时存在皮肤毛细血管扩张，怀疑为遗传性出血性毛细血管扩张症。文献回顾表明，在先前发表的12例涉及多发性动静脉畸形的病例中，有5次确立了该诊断。本文讨论了手术治疗的指征。
