Saylisoy Suzan, Incesulu Armagan, Gurbuz Melek Kezban, Adapinar Baki
From the *Department of Radiology, and †Department of Otorhinolaryngology, Faculty of Medicine, Eskisehir Osmangazi University, Meselik-Eskisehir, Turkey.
J Comput Assist Tomogr. 2014 Jan-Feb;38(1):20-4. doi: 10.1097/RCT.0b013e3182a0d05f.
Congenital mixed hearing loss associated with fixed stapes footplate is a rare disorder transmitted through X-linked inheritance. The purpose of this study was to report the radiologic findings of X-linked deafness with middle ear anomalies in affected children and young patients and in carrier women.
The computed tomographic and audiometric findings of 7 subjects (4 affected children and young patients, 1 of whom is a girl; 2 carrier mothers; and a man who presented with sudden hearing loss) from different families were analyzed.
Computed tomography showed bulbous dilatation of the fundi of the internal auditory canals, incomplete bony separation between the basal turn of the cochleas and the lateral ends of the internal auditory canal, deficiency of the modiolus, enlarged first part of the facial nerve, and dilatation of the superior and the inferior vestibular nerve canal and the singular canal. Besides these characteristic findings, dilatation of the vestibular aqueduct was seen except in the man. Middle ear anomalies including oval and/or round window and/or stapes abnormalities were also detected in three affected patients. The carrier mothers had milder forms of some characteristic findings.
Because of the risks of stapes surgery in X-linked deafness, recognition of the characteristic imaging features of these disorders is important. Especially in young patients with mixed hearing loss, temporal bone computed tomography should be performed before stapes surgery to avoid the complication of stapes gusher. Middle ear anomalies might be highly associated with X-linked deafness.
与镫骨底板固定相关的先天性混合性听力损失是一种通过X连锁遗传传递的罕见疾病。本研究的目的是报告受影响儿童、年轻患者以及携带者女性中伴有中耳异常的X连锁耳聋的影像学表现。
分析了来自不同家庭的7名受试者(4名受影响的儿童和年轻患者,其中1名是女孩;2名携带者母亲;以及一名突发听力损失的男性)的计算机断层扫描和听力检查结果。
计算机断层扫描显示内耳道底部呈球茎状扩张,耳蜗底转与内耳道外侧端之间的骨质分隔不完全,蜗轴缺失,面神经第一部分增粗,前庭上、下神经通道及单孔管扩张。除这些特征性表现外,除该男性外,均可见前庭导水管扩张。在3名受影响的患者中还检测到中耳异常,包括椭圆窗和/或圆窗及/或镫骨异常。携带者母亲的一些特征性表现形式较轻。
由于X连锁耳聋患者进行镫骨手术存在风险,识别这些疾病的特征性影像学表现很重要。特别是对于混合性听力损失的年轻患者,在进行镫骨手术前应进行颞骨计算机断层扫描,以避免镫骨井喷并发症。中耳异常可能与X连锁耳聋高度相关。