Sawamura Y, Nakagawa Y, Ikota T, Abe H
Department of Neurosurgery, Hokkaido University School of Medicine, Sapporo, Japan.
J Neurosurg. 1989 Oct;71(4):611-5. doi: 10.3171/jns.1989.71.4.0611.
Neurinomas arising from the peripheral branch of the acoustic nerve distal to the internal auditory canal in the temporal bone are rare. Two advanced skull-base neurinomas are described which were situated mainly in the temporal petrous bone, and extended to the parapharyngeal space anteriorly, to the lateral cervical portion inferiorly, into the sphenoidal sinus medially, and into the middle and posterior cranial fossae compressing the brain stem. Both patients had been deaf for several years without other neurological deficits. The operative findings revealed that the fifth, seventh, and caudal cranial nerves were intact; therefore, it was suspected that these neurinomas originated primarily within the cochlea or the vestibule in the temporal bone. The tumors were completely removed via an extradural approach, with good results. Since the surgical treatment of such advanced skull-base neurinomas is difficult, the operative infratemporal fossa approach is described in detail.
起源于颞骨内耳道远端听神经外周分支的神经鞘瘤很罕见。本文描述了两例晚期颅底神经鞘瘤,它们主要位于颞骨岩部,向前延伸至咽旁间隙,向下延伸至颈外侧部,向内侧延伸至蝶窦,并延伸至中颅窝和后颅窝压迫脑干。两名患者均已失聪数年,无其他神经功能缺损。手术结果显示,第五、第七和尾侧颅神经完好;因此,怀疑这些神经鞘瘤主要起源于颞骨内的耳蜗或前庭。通过硬膜外入路将肿瘤完全切除,效果良好。由于此类晚期颅底神经鞘瘤的手术治疗困难,本文详细描述了颞下窝手术入路。