Kawakami K, Kawamoto K, Sakai N, Matsumoto K, Miya F, Kawamura Y, Tsuji H
Department of Neurosurgery, Kansai Medical University, Moriguchi, Japan.
No Shinkei Geka. 1992 Aug;20(8):909-14.
We presented a case of neurofibromatosis associated with intractable arteriovenous fistula of the internal carotid artery in the skull base. A 41-year-old man presenting dyspnea and neck swelling was treated with balloon occlusion for arteriovenous fistula. This was followed by its total removal. At operation, we found that arteriovenous fistula was formed by the invasion of the internal carotid arterial wall of a neurofibroma in the skull base, which had been induced by neurofibromatosis. This is a rare case corresponding to vascular neurofibromatosis in the internal carotid artery.
我们报告了一例神经纤维瘤病合并颅底颈内动脉顽固性动静脉瘘的病例。一名41岁男性因呼吸困难和颈部肿胀就诊，接受了动静脉瘘的球囊闭塞治疗，随后将其完全切除。手术中，我们发现动静脉瘘是由颅底神经纤维瘤侵犯颈内动脉壁形成的，该神经纤维瘤由神经纤维瘤病引起。这是一例罕见的颈内动脉血管神经纤维瘤病病例。
