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分阶段联合入路切除巨大后颅窝及颞骨神经鞘瘤。

Staged and Combined Approach for Resection of Giant Posterior Fossa and Temporal Bone Schwannoma.

机构信息

Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, Utah, USA.

Division of Otolaryngology, Department of Surgery, University of Utah, Salt Lake City, Utah, USA.

出版信息

World Neurosurg. 2022 Oct;166:170. doi: 10.1016/j.wneu.2022.07.115. Epub 2022 Aug 8.

DOI:10.1016/j.wneu.2022.07.115
PMID:35948215
Abstract

Vestibular schwannomas have an estimated incidence of 1.09/100,000 people, representing 6%-10% of intracranial tumors. Rarer giant vestibular schwannomas are defined by an extrameatal diameter of ≥4 cm and can be difficult to treat because of displacement and compression of local neurovasculature and the potential for multicompartment involvement. A 20-year-old woman with history of presumed right-sided Bell palsy and unexplained hearing loss was found to have a 9 × 8 × 6-cm giant posterior fossa schwannoma on syncopal workup (Video 1). It extended from the Meckel cave anterosuperiorly to below the skull base through the jugular foramen, filling the petrous apex and compressing the cerebellum, pons, and midbrain. She had ipsilateral facial weakness (House-Brackmann 3/5), V2 numbness, tongue deviation, vocal fold paresis, and hearing loss. A combined petrosal (transotic, extended middle fossa) and retrosigmoid approach was performed through a curvilineal incision that provided access to the middle fossa, petrous apex, and posterior fossa down to the jugular foramen and included a trajectory along the long axis of the tumor (retrosigmoid). Although we hypothesize this was a vestibular schwannoma, it was difficult to ascertain the exact origin of the tumor because of its massive size. Surgery was performed in 2 stages because of the large tumor size and to limit blood loss. A gross total resection was achieved. Closure included an autologous fat and synthetic cranioplasty. The patient was neurologically stable postoperatively, except for transient swallowing difficulty due to partial cranial nerve IX/X palsies. This case illustrates important considerations when combining surgical approaches for complex tumors involving multiple intracranial compartments.

摘要

前庭神经鞘瘤的发病率估计为每 10 万人中有 1.09 例,占颅内肿瘤的 6%-10%。罕见的巨大前庭神经鞘瘤的定义为外听道直径≥4cm,由于局部神经血管的移位和压迫以及多腔室受累的可能性,治疗较为困难。一名 20 岁女性,既往右侧贝尔麻痹和不明原因听力损失,在晕厥检查时发现右侧后颅窝有一个 9×8×6cm 的巨大神经鞘瘤(视频 1)。它从前上方的 Meckel 腔延伸到颅底下方的颈静脉孔,填满岩骨尖,压迫小脑、脑桥和中脑。她同侧面部无力(House-Brackmann 3/5)、V2 麻木、舌偏、声带麻痹和听力损失。通过曲线切口进行了联合岩骨(经颅窝、扩展中颅窝)和乙状窦后入路,该切口提供了从中颅窝、岩骨尖和后颅窝到达颈静脉孔的通道,包括沿着肿瘤长轴的轨迹(乙状窦后)。尽管我们假设这是一个前庭神经鞘瘤,但由于肿瘤体积巨大,很难确定肿瘤的确切来源。由于肿瘤体积大,为了限制出血,手术分两阶段进行。实现了大体全切除。闭合包括自体脂肪和合成颅骨成形术。患者术后神经功能稳定,除了因部分颅神经 IX/X 麻痹导致短暂吞咽困难外。该病例说明了在涉及多个颅内腔室的复杂肿瘤中结合手术方法时需要考虑的重要问题。

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