一例巨大前庭分裂瘤患者的独特外展神经重复变体

Ufuk Erginoglu, Mario Wolak Junior, Cagdas Ataoglu, Abdullah Keles, Mustafa K. Baskaya
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引用次数: 0

摘要

前庭分裂瘤(VS)是一种生长缓慢的良性肿瘤,常见于小脑视角,有可能压迫大脑结构和颅神经,包括负责侧视的外展神经(AN)。虽然大的VS可能会压迫AN,但手术后AN麻痹的情况并不多见,AN变异的临床意义,尤其是VS病例中的AN变异,仍不清楚。我们报告了一例独特的病例,患者是一名 29 岁女性,患有左侧前庭大面积分裂瘤。患者接受了左侧显微外科两期切除术,术后恢复顺利(House-Brackmann 面部分级 I 级)。在手术过程中,发现了一种罕见的前庭裂隙瘤变异。这条AN起源于两条独立的主干,在同一节段起源远端3毫米处合并。据我们所知,AN变异在蝶骨段的起源和合并以前从未报道过。识别AN变异对颅底手术的成功至关重要,尤其是在前庭裂孔瘤手术中保留两个分支并确保眼部功能。
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A unique variant of abducens nerve duplication in a case of a large vestibular schwannoma

Vestibular schwannomas (VS) are slow-growing benign tumors commonly found in the cerebellopontine angle, potentially compressing brain structures and cranial nerves, including the abducens nerve (AN), responsible for lateral gaze. Although large VSs may compress the AN, postsurgical AN palsy is rare, and the clinical significance of AN variations, particularly in VS cases, remains unclear. We report a unique case of a 29-year-old female with a large left vestibular schwannoma. The patient underwent a left-sided microsurgical two-stage excision with an uneventful recovery (House-Brackmann facial grade I). During surgery, a rare variant of the AN was identified. This AN originated as two separate trunks and merged 3 mm distal to its origin in the same segment. To the best of our knowledge, arising and merging in the cisternal segment of AN variation has not been reported previously. Recognizing AN variations is vital for successful skull base surgeries, especially in preserving both branches during vestibular schwannoma surgery and ensuring ocular function.

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CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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