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双侧内耳道伴面神经和前庭蜗神经功能障碍。

Duplicate internal auditory canals with facial and vestibulocochlear nerve dysfunction.

作者信息

Kew T Y, Abdullah A

机构信息

Department of Radiology, Medical Faculty, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.

出版信息

J Laryngol Otol. 2012 Jan;126(1):66-71. doi: 10.1017/S0022215111002258. Epub 2011 Aug 26.

Abstract

OBJECTIVE

We report an extremely rare case of duplication of the internal auditory canal associated with dysfunction of both the facial and vestibulocochlear nerves. We also review the literature regarding the integrity of the facial and vestibulocochlear nerves in such cases.

CASE REPORT

A 34-year-old man presented with unilateral, right-sided, sensorineural hearing loss and facial nerve palsy since childhood. Facial nerve function was observed to be House-Brackmann grade III. Computed tomography and magnetic resonance imaging demonstrated ipsilateral duplicate, vacant internal auditory canals. Based on the clinical presentation, we interpreted these radiological findings as aplasia of the vestibulocochlear nerve and severe hypoplasia of the facial nerve.

CONCLUSION

To our best knowledge, this is the first report of vestibulocochlear nerve aplasia and severe facial nerve hypoplasia in a case of ipsilateral duplication of the internal auditory canal. High resolution gradient echo magnetic resonance imaging sequences are advocated for assessment of neural integrity in patients with an abnormal internal auditory canal and facial and/or vestibulocochlear nerve dysfunction.

摘要

目的

我们报告一例极为罕见的内耳道重复病例,该病例伴有面神经和前庭蜗神经功能障碍。我们还回顾了有关此类病例中面神经和前庭蜗神经完整性的文献。

病例报告

一名34岁男性自童年起出现单侧右侧感音神经性听力损失和面神经麻痹。观察到面神经功能为House-Brackmann III级。计算机断层扫描和磁共振成像显示同侧存在重复的、空的内耳道。基于临床表现,我们将这些影像学表现解释为前庭蜗神经发育不全和面神经严重发育不良。

结论

据我们所知,这是首例内耳道同侧重复病例中前庭蜗神经发育不全和严重面神经发育不良的报告。对于内耳道异常且伴有面神经和/或前庭蜗神经功能障碍的患者,建议采用高分辨率梯度回波磁共振成像序列评估神经完整性。

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