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Management strategies for bilateral vestibular schwannomas.

机译:双侧前庭神经鞘瘤的治疗策略。

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BACKGROUND: Bilateral vestibular schwannomas (VS) are rare. Most patients in India present late in the course of illness with large tumors and disabling deafness. Clinical presentation and management goals are different from that of unilateral VS. AIMS: To highlight the differences in clinical presentations and surgical results of bilateral VS compared to unilateral VS; and, to propose a management strategy for these tumors with reference to tumor size, extent of growth and the presence or absence of hearing impairment. METHOD: This is a retrospective study of 16 patients with bilateral VS treated over 10 years in a tertiary referral hospital. Assessment of VIIth and VIIIth cranial nerve function, tumor size, volume and extent of growth was performed in all patients. The management strategy was based on Samii's classification of tumor extent. All patients were operated using a retromastoid suboccipital approach. Postoperative results were analyzed and compared with those of unilateral VS. RESULTS: The mean age of presentation was 25.7 years. Hearing impairment was the commonest symptom. Headache with features of raised intracranial pressure were present in 10 (62.5%) patients. Giant tumors were present in seven (43.7%) patients; large tumors in eight (50%) and a medium-sized tumor in one (6.3%). Total tumor resection was achieved in 13 patients and subtotal resection in two. One patient was managed conservatively and followed up with serial CT scans. On the contralateral side, one large tumor required total excision. One medium sized tumor underwent sub-capsular excision in an attempt to preserve hearing. The facial nerve was anatomically preserved in seven (46.7%) patients and in one, the cochlear nerve was anatomically preserved. There was no peri-operative mortality. CONCLUSIONS: Patients with bilateral schwannomas are younger, have larger lesions, poorer preoperative hearing and are more likely to lose either auditory and/or facial nerve function during attempted total resection of the tumor. Classifying the tumors into two groups by extent, that is, tumors extending to the cerebellopontine angle cistern (T1-T3a) and, tumors extending to or compressing the brainstem (T3b to T4b), allows the surgical strategy to be defined.
机译:背景:双边前庭神经鞘瘤(VS)是罕见的。印度的大多数患者在病程晚期出现大肿瘤,致残耳聋。临床表现和管理目标与单方面VS不同。目的:强调双侧VS与单侧VS相比在临床表现和手术结果上的差异;并针对肿瘤的大小,生长程度以及是否存在听力障碍提出治疗策略。方法:这是对三级转诊医院治疗10年以上的16例双侧VS患者的回顾性研究。在所有患者中评估了第七和第八颅神经功能,肿瘤大小,体积和生长程度。治疗策略基于Samii对肿瘤范围的分类。所有患者均采用后乳突后枕入路手术。对术后结果进行分析,并与单侧VS进行比较。结果:平均呈报年龄为25.7岁。听力障碍是最常见的症状。 10(62.5%)位患者出现了具有颅内压升高特征的头痛。七名(43.7%)患者中出现巨瘤;大型肿瘤占8个(50%),中等肿瘤占1个(6.3%)。 13例患者完成了肿瘤全切除,而2例则进行了大体切除。保守治疗一名患者,并进行连续CT扫描。在对侧,一个大肿瘤需要完全切除。为了保持听力,对一个中等大小的肿瘤进行了包膜下切除术。面部神经在解剖学上保留了七名(46.7%)患者,其中一位患者在解剖学上保留了耳蜗神经。没有围手术期死亡率。结论:双侧神经鞘瘤患者年龄较小,病变较大,术前听力较差,并且在尝试完全切除肿瘤期间更有可能失去听觉和/或面神经功能。将肿瘤按程度分为两类,即延伸至小脑桥脑池的肿瘤(T1-T3a)和延伸至或压缩脑干的肿瘤(T3b至T4b),可以确定手术策略。

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