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先天性外耳道闭锁面神经管的影像学研究。

An imaging study of the facial nerve canal in congenital aural atresia.

作者信息

Zhao Shouqin, Han Demin, Wang Zhenchang, Li Jie, Qian Yanni, Ren Yuanyuan, Dong Jiyong

机构信息

Department of Otolaryngology-Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, No. 1 Dong Jiao Min Xiang Rd., Dong Cheng District, Beijing, China 100730.

出版信息

Ear Nose Throat J. 2015 Oct-Nov;94(10-11):E6-13.

Abstract

We conducted a prospective study to investigate the abnormalities of the facial nerve canal in patients with congenital aural atresia by computed tomography (CT). Our study population was made up of 99 patients--68 males and 31 females, aged 6 to 22 years (mean: 13.5)--who had unilateral congenital aural atresia without any inner ear malformations. We compared our findings in these patients with those in 50 controls-33 males and 17 females, aged 5 to 22 years (mean: 15.0)-who had normal ears. We classified the congenital aural atresia patients into three groups (A, B, and C) according to their Jahrsdoerfer grading scale score (≥8; 6 or 7; and ≤5, respectively). The course of the facial nerve canal in both the controls and the study patients was determined by temporal bone CT with multiplanar reconstruction. The distances from different parts of the facial nerve canal to surrounding structures were also measured. The course of the facial nerve canal in the normal ears did not vary much, and there were no statistically significant differences according to head side and sex. In groups B and C, the tympanic segment, mastoid segment, and angle of the second genu of the facial nerve canal were all significantly smaller than those of the controls (p < 0.01 in all cases). Statistically, the tympanic segment of the facial nerve canal in patients with congenital aural atresia was downwardly displaced. The mastoid segment of the facial nerve canal in these patients was more anterior than that of the controls. We conclude that congenital aural atresia is often accompanied by abnormalities of the facial nerve canal, especially in the tympanic segment, the mastoid segment, and the second genu. We found that the lower the Jahrsdoerfer score was, the shorter the tympanic segment was and the more forward the mastoid segment was.

摘要

我们进行了一项前瞻性研究,旨在通过计算机断层扫描(CT)调查先天性耳道闭锁患者面神经管的异常情况。我们的研究对象包括99例患者,其中男性68例,女性31例,年龄在6至22岁之间(平均:13.5岁),均为单侧先天性耳道闭锁且无任何内耳畸形。我们将这些患者的检查结果与50名对照者进行比较,对照者中男性33例,女性17例,年龄在5至22岁之间(平均:15.0岁),耳朵正常。我们根据Jahrsdoerfer分级量表评分将先天性耳道闭锁患者分为三组(A组、B组和C组)(分别为≥8分;6或7分;≤5分)。通过颞骨CT多平面重建确定对照组和研究患者面神经管的走行。还测量了面神经管不同部位与周围结构的距离。正常耳朵的面神经管走行变化不大,根据头侧和性别也无统计学显著差异。在B组和C组中,面神经管的鼓室段、乳突段和第二膝状弯曲角度均显著小于对照组(所有病例p<0.01)。从统计学角度来看,先天性耳道闭锁患者面神经管的鼓室段向下移位。这些患者面神经管的乳突段比对照组更靠前。我们得出结论,先天性耳道闭锁常伴有面神经管异常,尤其是鼓室段、乳突段和第二膝状弯曲处。我们发现Jahrsdoerfer评分越低,鼓室段越短,乳突段越靠前。

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