Suppr超能文献

颈部舌下神经鞘瘤:病例报告及文献综述

Hypoglossal Schwannoma of Neck: Case Report and Review of Literature.

作者信息

Plitt Aaron, El Ahmadieh Tarek Y, Bindal Shivani, Myers Larry, White Jonathan, Gluf Wayne

机构信息

Department of Neurological Surgery, University of Texas Southwestern, Dallas, Texas, USA.

School of Medicine, University of Texas Southwestern, Dallas, Texas, USA.

出版信息

World Neurosurg. 2018 Feb;110:240-243. doi: 10.1016/j.wneu.2017.11.069. Epub 2017 Nov 22.

Abstract

BACKGROUND

Schwannomas are benign, slow-growing neoplasms of the myelin-producing Schwann cells of peripheral nervous system that most commonly affect sensory nerves. Hypoglossal schwannomas, tumors of purely motor nerves, comprise <5% of all head and neck schwannomas. Since the first description of a hypoglossal schwannoma in 1933, there have been few case reports of extracranial origins. The most common location of an extracranial hypoglossal schwannoma is in the parapharyngeal space and can mimic paragangliomas. We describe the case of a woman presenting with an enlarging neck mass originally thought to be a paraganglioma but ultimately discovered to be a hypoglossal schwannoma at surgery.

CASE DESCRIPTION

A 63-year-old woman had a well-circumscribed, mobile, nontender, 3-cm firm mass at the mandibular angle. On computed tomography, the mass was at the level of the carotid bifurcation, splaying the branching vessels. It was further evaluated with magnetic resonance imaging, which revealed a homogeneous, T2-hyperintense, T1-isointense mass with homogeneous contrast enhancement and scant flow voids. Biopsy revealed a spindle cell mass with positive S-100 staining. She underwent resection with the mass originating from the hypoglossal nerve.

CONCLUSIONS

Hypoglossal schwannomas are rare lesions with a variable location along the course of the nerve. An extracranial lesion was described here, which was initially mistaken for a paraganglioma. Surgical resection is the consensus recommendation and is often well tolerated with low risk of long-term recurrence.

摘要

背景

施万细胞瘤是起源于外周神经系统产生髓磷脂的施万细胞的良性、生长缓慢的肿瘤,最常累及感觉神经。舌下神经施万细胞瘤是一种纯运动神经肿瘤,占所有头颈部施万细胞瘤的比例不到5%。自1933年首次描述舌下神经施万细胞瘤以来,颅外起源的病例报告很少。颅外舌下神经施万细胞瘤最常见的部位是咽旁间隙,可类似副神经节瘤。我们描述了一例女性患者,其颈部肿块逐渐增大,最初被认为是副神经节瘤,但手术时最终发现是舌下神经施万细胞瘤。

病例描述

一名63岁女性在下颌角处有一个边界清晰、可活动、无压痛的3厘米实性肿块。计算机断层扫描显示,肿块位于颈动脉分叉水平,使分支血管分开。进一步进行磁共振成像评估,结果显示为一个均匀的、T2高信号、T1等信号肿块,有均匀的对比增强且血流空洞较少。活检显示为梭形细胞肿块,S-100染色呈阳性。她接受了手术切除,肿块起源于舌下神经。

结论

舌下神经施万细胞瘤是罕见病变,沿神经走行位置多变。本文描述了一例颅外病变,最初被误诊为副神经节瘤。手术切除是一致推荐的治疗方法,通常耐受性良好,长期复发风险低。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验