双侧骨性耳蜗神经管狭窄伴听力阈接近正常1例。

Korean journal of audiology Pub Date : 2012-12-01 Epub Date: 2012-12-18 DOI:10.7874/kja.2012.16.3.141
Jae-Cheul Ahn, Shin-Hye Kim, Byung Yoon Choi
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引用次数: 1

摘要

先天性感音神经性听力损失患者在高分辨率颞骨计算机断层扫描中经常发现狭窄的骨性耳蜗神经管。但这种骨结构异常并不能决定耳蜗神经的功能结局。在这里,我们提出一个病例14个月大的女孩有狭窄的双侧骨耳蜗神经管。在核磁共振成像中,两个耳蜗神经被确定为完整的。此外,声学脑干反应阈值和听觉稳态反应显示听力阈值接近正常。因此,我们认为狭窄的骨性耳蜗神经管本身并不一定表明听力损失的严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A case with the bilateral narrow bony cochlear nerve canals associated with near normal hearing thresholds.

A case with the bilateral narrow bony cochlear nerve canals associated with near normal hearing thresholds.

A case with the bilateral narrow bony cochlear nerve canals associated with near normal hearing thresholds.

A case with the bilateral narrow bony cochlear nerve canals associated with near normal hearing thresholds.

The narrow bony cochlear nerve canal in high resolution temporal bone computed tomography is frequently found in patients of congenital sensorineural hearing loss. But this bony structural anomaly could not conclude the functional outcome of cochlear nerve. Here, we present a case of a 14-month-old girl having bilateral narrow bony cochlear nerve canals. In magnetic resonance imaging, both the cochlear nerves were identified to be intact. Moreover, acoustic brainstem response threshold and auditory steady state response revealed nearly normal hearing thresholds. Therefore, we suggest that the narrow bony cochlear nerve canal itself does not necessarily indicate a substantial degree of hearing loss.

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