内耳道发育不全伴双侧前庭耳蜗神经发育不全及面神经走行异常:1例报告及MRI表现。

IF 0.7 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal of Radiology Case Reports Pub Date : 2021-05-31 eCollection Date: 2021-05-01 DOI:10.3941/jrcr.v15i5.3912
Luiz Ricardo Araújo Uchôa, Licia Pacheco Luna, Luis Arthur Brasil Gadelha Farias, Debora Lilian Nascimento Lima, Pablo Picasso de Araujo Coimbra
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引用次数: 1

摘要

随着世界范围内人工耳蜗植入数量的增加,内耳道和耳蜗的评估变得越来越重要。这一区域的解剖研究是必不可少的人工耳蜗手术使用磁共振成像作为选择的方法。我们报告一例6岁男性病患,诊断为罕见的双侧内听道畸形,并伴有面神经异常及前庭耳蜗神经发育不全。本报告提出了识别这种罕见畸形的重要性,以进行适当的管理,并加强对可能的并发症的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Internal auditory canal hypoplasia associated with bilateral vestibulocochlear nerve aplasia and deviant facial nerve course: A case report and MRI findings.

The evaluation of internal auditory canals and cochlea has gained significant importance due to the increasing number of cochlear implantations worldwide. This region's anatomical study is essential for cochlear implant surgery using magnetic resonance imaging as the method of choice. We report a case of a 6-year-old male patient diagnosed with a rare bilateral malformation of the internal auditory canals associated with an aberrant course of the facial nerve and vestibulocochlear nerve aplasia. This report raises the importance of identifying this rare malformation for appropriate management and reinforces awareness of possible complications.

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来源期刊
Journal of Radiology Case Reports
Journal of Radiology Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
1.10
自引率
0.00%
发文量
25
审稿时长
24 weeks
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