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卵圆窗先天性畸形:放射学诊断及手术技术经验

Congenital malformation of the oval window: experience of radiologic diagnosis and surgical technique.

作者信息

Yang Feng, Liu Yang, Sun Jianjun, Li Jinrang, Song Rendong

机构信息

Department of Otolaryngology, The Second Central Hospital, Baoding, Fanyang Road 57, Zhuozhou, 072750, Hebei, China.

Center of Otolaryngology, PLA Navy General Hospital, Fucheng Road 6, Haidian District, Beijing, 100048, China.

出版信息

Eur Arch Otorhinolaryngol. 2016 Mar;273(3):593-600. doi: 10.1007/s00405-015-3597-6. Epub 2015 Mar 13.

Abstract

The aim of this study was to introduce and discuss the method of preoperative radiological diagnosis to the congenital absence or atresia of the oval window (OW), and the method of surgical treatment. From July 2010 through August 2014, patients with normal external canal and tympanic membrane but conductive hearing loss underwent high resolution CT scan (HRCT). The multi-planar reformation (MPR), a post-processing protocol, was used. The patients with diagnosis of OW atresia and malformed stapes preoperatively underwent surgical treatment. The vestibular drilled-out and promontory drilled-out technique was used to reconstruct the ossicular chain. In the preoperative radiological diagnosis, six patients (ears) were noted to have congenital absence or atresia of the oval window with malformed facial nerve (class 4) and two patients (ears) were found to have footplate fixation (class 2). In the surgical treatment of eight ears, the malformed structure was identified and the ossicular chain reconstruction was made in six ears. The coronal HRCT CT imaging and the MPR post-processing technique can provide us practical and definite information for surgical treatment, especially in the discrimination of OW atresia and the fixed stapedal footplate. The promontory drill-out technique, fenestration in the bottom of the basal turn, provides us a new method in the hearing reconstruction when the area of OW was fully covered by malformed facial nerve. This technique was first reported in the literature.

摘要

本研究的目的是介绍并讨论先天性卵圆窗缺失或闭锁的术前放射学诊断方法以及手术治疗方法。2010年7月至2014年8月,对外耳道及鼓膜正常但有传导性听力损失的患者进行了高分辨率CT扫描(HRCT)。采用了一种后处理方案——多平面重建(MPR)。术前诊断为卵圆窗闭锁及镫骨畸形的患者接受了手术治疗。采用前庭开窗和岬开窗技术重建听骨链。在术前放射学诊断中,6例患者(耳)被发现有先天性卵圆窗缺失或闭锁伴面神经畸形(4级),2例患者(耳)有镫骨足板固定(2级)。在8耳的手术治疗中,识别出畸形结构并对6耳进行了听骨链重建。冠状位HRCT成像及MPR后处理技术可为手术治疗提供实用且明确的信息,尤其是在鉴别卵圆窗闭锁和固定的镫骨足板方面。岬开窗技术,即在鼓室底开窗,为卵圆窗区域被畸形面神经完全覆盖时的听力重建提供了一种新方法。该技术首次在文献中报道。

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