Murata J, Abe H, Aida T, Miyamachi K, Miyasaka K
Department of Neurosurgery, Hokkaido University School of Medicine.
No Shinkei Geka. 1991 May;19(5):455-8.
A rare case of hemangioma of the petrous bone is described. A 31-year-old woman suffered from right facial twitching and palsy. So she underwent a craniectomy intending microvascular decompression of the facial nerve, but no compressing vessels or tumors were found. Three years later, however, her facial fasciculation disappeared spontaneously, but facial weakness deteriorated and she began to feel vertigo. On admission, neurological examination revealed right facial palsy of the peripheral type, slight hearing disturbance, and canal palsy. Bone-window CT and T2-weighted MRI revealed a small tumor destroying the petrous bone near the geniculate portion of the facial nerve. Using the epidural subtemporal approach, the tumor was totally removed and the facial nerve remained intact. Histologically it was diagnosed as hemangioma. Hemangioma of the skull base bone is rare, and it is interesting that the tumor in this case caused abnormal facial contraction like hemifacial spasm.
本文描述了一例罕见的岩骨血管瘤病例。一名31岁女性患有右侧面部抽搐和面瘫。因此,她接受了颅骨切除术,打算对面神经进行微血管减压,但未发现压迫血管或肿瘤。然而,三年后,她的面部肌束震颤自行消失,但面部无力恶化,并且开始感到眩晕。入院时,神经系统检查发现右侧周围性面瘫、轻度听力障碍和管麻痹。骨窗CT和T2加权MRI显示一个小肿瘤,破坏了面神经膝状部附近的岩骨。采用硬膜外颞下入路,肿瘤被完全切除,面神经保持完整。组织学诊断为血管瘤。颅底骨血管瘤罕见,有趣的是,该病例中的肿瘤引起了类似半面痉挛的面部异常收缩。