Asymptomatic Purely Intracranial Vagal Schwannoma: Clinical Case Report and Literature Review.

Zhong Yao, Shuo Xu
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Abstract

Vagus nerve schwannoma is an infrequently occurring schwannoma, in which a distinct subtype exists wherein the tumor is confined to the cerebellomedullary cistern without invading the jugular foramen. This unique tumor is called purely intracranial vagal schwannoma. In this case report, we present a case of purely intracranial vagal schwannoma in its asymptomatic early phase, incidentally discovered during surgery performed on a patient with hemifacial spasm. Because of the small size of the tumor, we definitively recognized that it originated from the second rootlet on the caudal side. The tumor was totally resected uneventfully and a favorable prognosis was achieved. Furthermore, we conducted a comprehensive literature review to summarize the classification, origin, and surgical complications associated with this rare tumor type. Based on our literature review, we propose that: 1) the origin of tumor is related to the time of onset of symptoms, 2) nearly all purely intracranial vagal schwannomas can be entirely resected and favorable prognosis can be achieved, and 3) surgeons should be aware of potential cardiovascular complications during surgical procedures.

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无症状纯颅内迷走神经丛神经瘤:临床病例报告和文献综述。
背景:迷走神经分裂瘤是一种不常发生的分裂瘤,其中有一种独特的亚型,即肿瘤局限于小脑髓腔而不侵犯颈静脉孔。这种独特的肿瘤被称为纯颅内迷走神经分裂瘤。临床表现:在本报告中,我们介绍了一例无症状早期纯颅内迷走神经分裂瘤病例,该病例是在为一名半面痉挛患者进行手术时偶然发现的。由于肿瘤体积较小,我们最终确定它来自尾侧的第二根小根。肿瘤被顺利完全切除,预后良好。此外,我们还进行了全面的文献综述,总结了这种罕见肿瘤的分类、起源和手术并发症。结论:据我们所知,这是第一例无症状纯颅内迷走神经分裂瘤的病例报告。根据文献综述,我们认为1)肿瘤的来源与症状出现的时间有关;2)几乎所有的纯颅内迷走神经分裂瘤都可以完全切除,并获得良好的预后;3)外科医生在手术过程中应注意潜在的心血管并发症。
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