Horimoto C, Baba H, Kawano T, Shibata S, Mori K, Nakajima S, Kumagami H
Department of Neurosurgery, Nagasaki University, Japan.
No Shinkei Geka. 1987 Oct;15(10):1133-8.
Facial nerve schwannoma is rare. Since the first description by Schmid, about 150 cases have been reported mainly in the otological field. The authors recently had a case of facial nerve schwannoma with a marked capsular calcification, extending into the middle cranial fossa. A 63-year-old man was admitted to our hospital on June 20, 1986. About 44 years prior to the admission, he noted facial weakness of the right side which gradually progressed. Neurological examination on admission revealed complete right facial paralysis of the peripheral type with loss of taste, right hearing loss, diminution of lacrimal secretion and no reaction to caloric stimulation. Stenvers' view and tomogram of the right temporal bone showed destruction of petrous ridge. CT scan demonstrated bony destruction of the right petrous pyramid and high dense mass lesion, extending into the middle cranial fossa. Peritumoral and intratumoral calcifications, characteristics of facial nerve schwannoma were also noted. Right external carotid angiography demonstrated the tumor was fed by petrous branch of the right middle meningeal artery. On July 11, 1986 right temporal craniotomy and extradural approach to the floor of the petrous portion of the middle cranial fossa were performed. There was an extradural mass which extended to the middle cranial fossa through the destroyed pyramis. The tumor appeared to originate from the geniculate ganglion of the facial nerve and invaded the inner and middle ear which were almost completely removed. Operative specimen demonstrated that the tumor was a schwannoma. Postoperative hearing test and facial nerve function showed no changes as compared with preoperative findings. Similar case reports with CT findings were reviewed.
面神经鞘瘤较为罕见。自施密德首次描述以来,主要在耳科学领域已报道了约150例。作者近期遇到一例面神经鞘瘤,伴有明显的包膜钙化,并延伸至中颅窝。一名63岁男性于1986年6月20日入住我院。入院前约44年,他注意到右侧面部无力,且逐渐加重。入院时的神经学检查显示为完全性右侧周围性面瘫,伴有味觉丧失、右耳听力丧失、泪液分泌减少以及对冷热刺激无反应。右侧颞骨的斯滕弗斯位片和体层摄影显示岩骨嵴破坏。CT扫描显示右侧岩骨锥体骨质破坏及高密度肿块病变,延伸至中颅窝。还注意到瘤周和瘤内钙化,这是面神经鞘瘤的特征。右侧颈外动脉血管造影显示肿瘤由右侧脑膜中动脉的岩支供血。1986年7月11日,实施了右侧颞骨开颅术及经硬膜外入路至中颅窝岩部底面。有一个硬膜外肿块,通过被破坏的锥体延伸至中颅窝。肿瘤似乎起源于面神经膝状神经节,并侵犯了几乎被完全切除的内耳和中耳。手术标本显示该肿瘤为神经鞘瘤。术后听力测试及面神经功能与术前结果相比无变化。对有CT表现的类似病例报告进行了回顾。