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耳蜗发育不良:放射学评估与听力康复选择。

Aplasia of the cochlea: radiologic assessment and options for hearing rehabilitation.

机构信息

Department of Otolaryngology, , Hannover Medical School, Hannover, Germany.

出版信息

Otol Neurotol. 2013 Sep;34(7):1253-60. doi: 10.1097/MAO.0b013e318291c48f.

DOI:10.1097/MAO.0b013e318291c48f
PMID:23928521
Abstract

OBJECTIVE

Hearing rehabilitation of patients with severe inner ear malformations remains controversial. Our objective was to describe the radiologic findings of aplasia of the cochlea (AC) and evaluate the existing therapeutic options in such patients.

STUDY DESIGN

Retrospective cohort study.

SETTING

Tertiary referral center.

PATIENTS

Pediatric and adult patients with AC evaluated at our institution from 1995 to 2010.

INTERVENTIONS

The precise radiologic findings were identified using high-resolution computed tomography (HRCT) and magnetic resonance imaging (MRI) scans of the inner ear. In cases of auditory implantation on the AC side, the achieved outcome was recorded using categories of auditory performance (CAP). Related surgical aspects were analyzed.

RESULTS

Twenty-three patients (28 ears) with AC were found. In 5 patients AC was bilateral. The remaining unilateral cases had contralateral normal ears (2 patients), cochlea hypoplasia (5 patients), common cavity (6 patients), incomplete partition Type I (4 patients), and atresia of the internal auditory canal (1 patient). Four patients (3 bilateral, 1 unilateral ACs) were treated with cochlear implants in ears with AC, and 1 patient underwent auditory brainstem implantation. All implanted patients achieved speech perception with limited vocabulary (CAP scores between 4 and 5).

CONCLUSION

AC is defined as the total absence of the cochlea, with a present, although malformed, vestibule. Although a distinct auditory nerve was not seen in these cases of AC, results following cochlear implantation suggest functional cochlear nerve fibers in the remaining dysplastic inner ear structures. In selected cases, cochlear implantation may be a reasonable option for the habilitation of deafness associated with AC.

摘要

目的

内耳畸形患者的听力康复仍然存在争议。我们的目的是描述耳蜗发育不全(AC)的放射学表现,并评估此类患者的现有治疗选择。

研究设计

回顾性队列研究。

设置

三级转诊中心。

患者

1995 年至 2010 年在我院接受 AC 评估的儿科和成人患者。

干预措施

使用内耳高分辨率计算机断层扫描(HRCT)和磁共振成像(MRI)扫描来确定准确的放射学发现。在 AC 侧进行听觉植入的情况下,使用听觉表现类别(CAP)记录所获得的结果。分析了相关的手术方面。

结果

发现 23 例(28 耳)AC 患者。5 例患者为双侧 AC。其余单侧病例对侧为正常耳朵(2 例)、耳蜗发育不全(5 例)、共同腔(6 例)、不完全分隔Ⅰ型(4 例)和内听道闭锁(1 例)。4 例患者(3 例双侧 AC,1 例单侧 AC)在 AC 耳中接受了耳蜗植入治疗,1 例患者接受了听觉脑干植入治疗。所有植入患者均通过有限词汇的言语感知获得(CAP 评分在 4 到 5 之间)。

结论

AC 被定义为耳蜗完全缺失,但前庭存在,尽管发育不良。尽管在这些 AC 病例中没有看到明显的听神经,但耳蜗植入后的结果表明,在剩余的发育不良内耳结构中存在功能性耳蜗神经纤维。在选择的病例中,耳蜗植入可能是与 AC 相关耳聋康复的合理选择。

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