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舌咽神经鞘瘤:百年回顾

Glossopharyngeal schwannomas: a 100 year review.

作者信息

Vorasubin Nopawan, Sang U Hoi, Mafee Mahmood, Nguyen Quyen T

机构信息

University of California, San Diego School of Medicine, La Jolla, California, USA.

出版信息

Laryngoscope. 2009 Jan;119(1):26-35. doi: 10.1002/lary.20045.

Abstract

OBJECTIVES

To review the literature on glossopharyngeal schwannomas with a focus on clinical presentation, radiologic/audiologic characteristics, and management options, and to propose a mechanism explaining the nature of vestibulocochlear dysfunction seen with these tumors.

STUDY DESIGN

Contemporary review.

METHODS

English literature search for cases of primary isolated glossopharyngeal schwannomas and chart review of two new cases.

RESULTS

A total of 42 glossopharyngeal schwannoma cases between 1908-2008 were reviewed. Of these 84% presented with vestibulocochlear symptoms whereas only 30% presented with glossopharyngeal symptoms. Tumors can occur anywhere along the CNIX; however, the majority of symptomatic cases are intracranial/intraosseous, which present with vestibulocochlear dysfunction. Reviewed cases typically described the caliber of CNVII and VIII on CT/MRI as normal. We present a case where notching and displacement of CNVIII by the tumor can be appreciated on MRI, allowing for the first correlation between clinical symptoms and imaging findings. Mid frequency SNHL was prevalent in contrast to the high-frequency pattern typical of vestibular schwannomas. Tonotopic studies of CNVIII mapped low-to-mid frequency fibers along the posterior medial surface corresponding to the area of greatest compression by glossopharyngeal schwannomas.

CONCLUSION

Glossopharyngeal schwannomas usually present with vestibulocochlear rather than glossopharyngeal symptoms, likely due to CNVIII compression and displacement by tumor, which can be better appreciated with modern imaging. The tumor's location posterior and medial to CNVIII combined with the complex CNVIII tonotopic organization may account for the preferential mid-frequency hearing loss seen in these patients.

摘要

目的

回顾关于舌咽神经鞘瘤的文献,重点关注临床表现、放射学/听力学特征及治疗选择,并提出一种机制来解释这些肿瘤所导致的前庭蜗神经功能障碍的本质。

研究设计

当代综述。

方法

检索英文文献中原发性孤立性舌咽神经鞘瘤的病例,并对两例新病例进行病历回顾。

结果

回顾了1908年至2008年间共42例舌咽神经鞘瘤病例。其中84%出现前庭蜗神经症状,而只有30%出现舌咽神经症状。肿瘤可发生于舌咽神经的任何部位;然而,大多数有症状的病例为颅内/骨内型,表现为前庭蜗神经功能障碍。回顾的病例中,CT/MRI通常描述面神经和位听神经的管径正常。我们报告了一例病例,在MRI上可观察到肿瘤对位听神经的切迹和移位,这首次实现了临床症状与影像学表现之间的关联。与前庭神经鞘瘤典型的高频模式不同,中频感音神经性听力损失较为普遍。对位听神经的音频定位研究显示,低频至中频纤维沿后内侧表面分布,对应于舌咽神经鞘瘤最大压迫区域。

结论

舌咽神经鞘瘤通常表现为前庭蜗神经症状而非舌咽神经症状,可能是由于肿瘤对面听神经的压迫和移位,现代影像学能更好地观察到这一情况。肿瘤位于位听神经后方和内侧,加上位听神经复杂的音频定位组织,可能是这些患者出现中频听力损失的原因。

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