Onodera Hidetaka, Hiramoto Jun, Morishima Hiroyuki, Tanaka Yuichiro, Hashimoto Takuo
Department of Neurosurgery, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Neurol Med Chir (Tokyo). 2012;52(4):216-8. doi: 10.2176/nmc.52.216.
A 22-year-old woman developed an unruptured fusiform aneurysm of the internal carotid artery 7 months after being diagnosed with Wagener's granulomatosis. Intracranial aneurysmal formation is an extremely rare complication of Wegener's granulomatosis. This rare case of intracranial aneurysm was treated by endovascular balloon occlusion.
一名22岁女性在被诊断为韦格纳肉芽肿7个月后,出现了颈内动脉未破裂的梭形动脉瘤。颅内动脉瘤形成是韦格纳肉芽肿极为罕见的并发症。这例罕见的颅内动脉瘤病例通过血管内球囊闭塞术进行了治疗。