Aref Mohammed, Kunigelis Katherine, Cass Stephen P, Youssef A Samy
Department of Neurosurgery, University of Colorado, Aurora, Colorado, United States.
Department of Otolaryngology, University of Colorado Hospital, Aurora, Colorado, United States.
J Neurol Surg B Skull Base. 2019 Jun;80(Suppl 3):S271. doi: 10.1055/s-0038-1673703. Epub 2018 Nov 26.
Vestibular schwannoma is a benign tumor that affects 3% of the population, but accounts for 85% of tumors occurring at the cerebellopontine angle (CPA). In this case, we present a 48-year-old female with history of cholesteatoma on the right and chronic suppurative otitis media on the left who presented with an 18 month history of bilateral hearing loss, worse on the right. Investigations revealed a right sided vestibular schwannoma measuring 1.6 cm in diameter. Audiogram revealed an AAO-HNS (American Academy of Otolaryngology-Head and Neck Surgery) class C hearing on the right and class B on the left. There are several management options for this size of vestibular schwannoma including observation and radiosurgery. However, preserving cochlear nerve function remains a challenging enterprise. Furthermore, the ideal management that confers the highest chance of hearing preservation remains heavily debated. Given the patient's young age, the goal of hearing preservation and the tumor size/extension into the CPA, surgery was decided through a right retrosigmoid transmeatal approach for tumor resection with intraoperative brain auditory evoked responses monitoring. For hearing preservation, we emphasize few important dissection techniques: tumor debulking from the top first to avoid early manipulation of the cochlear nerve at the bottom of the tumor, sharp dissection from medial to lateral off the vestibular nerve which is kept intact as a tension band to minimize cochlear nerve manipulations, and limit the drilling of the posterolateral wall of the internal auditory canal (IAC) medial to the labyrinth and endolymphatic apparatus. Postoperatively, the patient was discharged home within 2 days, with imaging showing a gross total resection. Follow-up audiogram shows unchanged pure tone thresholds. The link to the Video can be found at: https://youtu.be/Z5ftkpJN5k8 .
前庭神经鞘瘤是一种良性肿瘤,影响3%的人群,但占桥小脑角(CPA)肿瘤的85%。在此病例中,我们报告一名48岁女性,有右侧胆脂瘤和左侧慢性化脓性中耳炎病史,出现双侧听力下降18个月,右侧更严重。检查发现右侧有一个直径1.6 cm的前庭神经鞘瘤。听力图显示右侧为美国耳鼻咽喉头颈外科学会(AAO-HNS)C级听力,左侧为B级。对于这种大小的前庭神经鞘瘤有多种治疗选择,包括观察和放射外科手术。然而,保留蜗神经功能仍然是一项具有挑战性的工作。此外,关于能赋予最高听力保留机会的理想治疗方法仍存在激烈争论。鉴于患者年轻、听力保留的目标以及肿瘤大小/向CPA的扩展情况,决定通过右侧乙状窦后经耳道入路进行手术切除肿瘤,并在术中进行脑听觉诱发电位监测。为了保留听力,我们强调一些重要的解剖技术:首先从顶部切除肿瘤组织以避免在肿瘤底部过早操作蜗神经,从前庭神经内侧向外侧进行锐性分离,将前庭神经作为张力带保持完整以尽量减少对蜗神经操作,并限制对内耳道(IAC)后外侧壁在迷路和内淋巴装置内侧的钻孔。术后,患者在2天内出院,影像学显示肿瘤全切。随访听力图显示纯音阈值未变。视频链接可在:https://youtu.be/Z5ftkpJN5k8 找到。