Complete Hearing Recovery after Retrosigmoid Resection of Jugular Foramen Schwannoma with Concurrent Ipsilateral Vestibular Schwannoma.

IF 0.6 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2025-02-06 eCollection Date: 2025-01-01 DOI:10.1055/a-2516-7311
Achilles A Kanaris, Nicholas E F Hac, Stephen T Magill, Kevin Y Zhan
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Abstract

Introduction  Cerebellopontine angle (CPA) tumors frequently present with hearing loss, which influences whether a hearing-preservation versus hearing ablative surgical approach is chosen. We discuss a case of complete hearing recovery after resection of a jugular foramen schwannoma (JFS) in a patient who also had a small intracanalicular vestibular schwannoma (VS). Case  A 46-year-old woman presented with left ear fullness, tinnitus, and imbalance for 9 months. She had no lower cranial nerve dysfunction. Audiometry demonstrated Class D hearing with 4% word recognition on the left. Vestibular testing showed absent caloric response on the left and subtle central findings. Magnetic resonance imaging demonstrated a left 3.3-cm JFS and separate left 1-cm intracanalicular VS. A retrosigmoid approach was performed for a radical subtotal resection of the JFS, relieving the mass effect on the vestibulocochlear nerve. The small intracanalicular VS was not manipulated. Pathology confirmed schwannoma with neurofibromatosis type 2 (NF2) mutation in the tumor but normal NF2 germline. Postoperative audiometry at 6 weeks showed normal audiometric thresholds with 100% discrimination. Subtle left caloric response was noted on postoperative vestibular testing and central oculomotor findings improved. Discussion  The presented case describes the management of concurrent ipsilateral VS and JFS in the absence of NF2 and demonstrates a unique complete and rapid recovery of hearing following JFS resection without manipulation of concurrent VS. This case supports the use of a hearing-preservation approach in similar cases and corroborates previous reports of hearing recovery following resection of non-VS CPA tumors with hearing-preservation approaches.

乙状窦后切除颈静脉孔神经鞘瘤并发同侧前庭神经鞘瘤后听力完全恢复。
摘要桥小脑角(CPA)肿瘤常伴有听力损失,这影响了选择听力保留还是听力消融手术。我们讨论一例颈静脉孔神经鞘瘤(JFS)切除术后听力完全恢复的病例,该患者同时患有小管内前庭神经鞘瘤(VS)。病例46岁女性,左耳充盈、耳鸣、失衡9个月。她没有下颅神经功能障碍。听力测试显示为D级听力,左侧有4%的单词识别。前庭测试显示左侧没有热反应,中央有细微的发现。磁共振成像显示左侧3.3 cm的JFS和左侧1 cm的管腔内vs,采用乙状结肠后入路对JFS进行根治次全切除,减轻了前庭耳蜗神经的肿块效应。小管内VS未被操纵。病理证实神经鞘瘤伴2型神经纤维瘤病(NF2)突变,但NF2种系正常。术后6周的听力测量显示听力阈值正常,判别率100%。术后前庭测试发现轻微的左热反应,中枢动眼肌结果改善。本病例描述了在没有NF2的情况下对并发同侧VS和JFS的处理,并展示了在不操纵并发VS的情况下,JFS切除后听力的独特完整和快速恢复。该病例支持在类似病例中使用听力保留方法,并证实了先前使用听力保留方法切除非VS CPA肿瘤后听力恢复的报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
12 weeks
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