Dağkıran Muhammed, Dağkıran Nermin, Sürmelioğlu Özgür, Ballı Tuğsan, Tuncer Ülkü, Akgül Erol, Çetik Fikret
Department of Otorhinolaryngology, Çukurova University School of Medicine, Adana, Turkey.
J Int Adv Otol. 2016 Apr;12(1):43-8. doi: 10.5152/iao.2015.1450.
The aim of this study was to determine and classify inner ear abnormalities in patients who had cochlear implants because of congenital sensorineural hearing loss using preoperative temporal bone computed tomography and magnetic resonance imaging.
Patients in the otolaryngology department who had cochlear implants because of congenital sensorineural hearing loss between January 2011 and December 2013 were included in the study. There were 167 male and 133 female patients, a total of 300. All of the patients were evaluated with 4-detector-row computed tomography and 1.5 Tesla magnetic resonance imaging.
Inner ear abnormalities were found in 136 of 600 ears (20.3%). There were six ears with incomplete partition-II (4.4%), five ears with incomplete partition-I (3.6%), two ears with Michel deformity (1.4%), two ears with cochlear hypoplasia (1.4%), two ears with cochlear otosclerosis (1.4%), and one ear with common cavity deformity (0.7%). Dilatation of the internal acoustic canal was found in 42 ears (30.9%); also, 21 ears with cochlear nerve aplasia/hypoplasia (15.4%), 5 ears with internal acoustic canal aplasia, and 1 ear with internal acoustic canal hypoplasia (0.73%) were detected. There were 10 ears with posterior semicircular canal (7.3%), 10 ears with lateral semicircular canal (7.4%), 8 ears with superior semicircular canal aplasia/hypoplasia (5.9%), and 8 ears with lateral semicircular canal-vestibular dysplasia. An enlarged vestibular aqueduct was found in 16 ears (11.7%). High jugular bulbs were found in 21 ears; however, this variation was not considered to be an inner ear abnormality.
Computed tomography and magnetic resonance imaging are essential for the evaluation, determination, and classification of inner ear abnormalities in patients with congenital sensorineural hearing loss who are candidates for cochlear implant operations. Also, these radiological instruments aid in determining contraindications and predicting intraoperative difficulties. Computed tomography and magnetic resonance imaging findings for these patients should be evaluated by an experienced radiologist before the operation.
本研究旨在利用术前颞骨计算机断层扫描和磁共振成像,确定并分类因先天性感音神经性听力损失而接受人工耳蜗植入的患者的内耳异常情况。
本研究纳入了2011年1月至2013年12月间因先天性感音神经性听力损失而在耳鼻喉科接受人工耳蜗植入的患者。其中男性患者167例,女性患者133例,共300例。所有患者均接受了4排螺旋计算机断层扫描和1.5特斯拉磁共振成像检查。
600只耳中发现内耳异常136只(20.3%)。其中不完全分隔-II型6只耳(4.4%),不完全分隔-I型5只耳(3.6%),米歇尔畸形2只耳(1.4%),耳蜗发育不全2只耳(1.4%),耳蜗耳硬化2只耳(1.4%),共同腔畸形1只耳(0.7%)。发现内耳道扩张42只耳(30.9%);此外,检测到耳蜗神经发育不全/发育不良21只耳(15.4%),内耳道发育不全5只耳,内耳道发育不良1只耳(0.73%)。后半规管发育异常10只耳(7.3%),外半规管发育异常10只耳(7.4%),上半规管发育不全/发育不良8只耳(5.9%),外半规管-前庭发育异常8只耳。发现扩大的前庭导水管16只耳(11.7%)。发现高位颈静脉球21只耳;然而,这种变异不被认为是内耳异常。
计算机断层扫描和磁共振成像对于评估、确定和分类先天性感音神经性听力损失且适合人工耳蜗植入手术的患者的内耳异常至关重要。此外,这些放射学检查有助于确定禁忌证并预测术中困难。这些患者的计算机断层扫描和磁共振成像结果应由经验丰富的放射科医生在手术前进行评估。