先天性卵圆窗闭锁截踝2例。

Korean journal of audiology Pub Date : 2013-12-01 Epub Date: 2013-12-13 DOI:10.7874/kja.2013.17.3.152
Sang Hyeon Ahn, Da Hee Kim, Jae Young Choi, Bo Gyung Kim
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引用次数: 4

摘要

先天性卵圆窗畸形伴面神经走行异常是一种罕见的胚胎学缺陷,与第二鳃裂衍生物发育不全有关。有一些改善听力水平的治疗方法;这些包括助听器、前庭切开术、新卵圆窗形成和镫骨手术,包括镫骨包括镫骨切开术和镫骨踝切开术。然而,手术治疗先天性卵圆窗异常很少被报道,通常是在非常小的患者系列中。我们报告两例先天性椭圆窗畸形伴面神经走行异常。1例为40岁男性,诊断为单侧先天性卵圆窗闭锁;另一为10岁男性,诊断为双侧先天性卵圆窗闭锁。我们同时也描述了面神经走行异常的先天性椭圆窗畸形的截踝术的临床表现和治疗结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Two cases of malleostapedotomy in congenital oval window atresia.

Two cases of malleostapedotomy in congenital oval window atresia.

Two cases of malleostapedotomy in congenital oval window atresia.

Congenital anomaly of the oval window with an abnormal facial nerve course is an uncommon embryological defect, which is related to the underdevelopment of second branchial arch derivatives. Some treatments for improving hearing levels are available; these include hearing aids, vestibulotomy, neo-oval window formation, and stapes surgeries, including incudostapedotomy and malleostapedotomy. However, surgery for congenital anomalies of the oval window has rarely been described, usually in very small series of patients. We describe two cases of congenital anomalies of the oval window with aberrant facial nerve courses. One was a 40-year-old male diagnosed with unilateral congenital oval window atresia; the other was a 10-year-old male diagnosed with bilateral congenital oval window atresia. We also describe the clinical manifestations and treatment outcomes of malleostapedotomy for congenital anomalies of the oval window with aberrant facial nerve courses.

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