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儿童罕见第三窗疾病的听觉前庭量化

Audiovestibular Quantification in Rare Third Window Disorders in Children.

作者信息

Dasgupta Soumit, Ratnayake Sudhira, Crunkhorn Rosa, Iqbal Javed, Strachan Laura, Avula Shivaram

机构信息

Department of Paediatric Audiology and Audiovestibular Medicine, Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom.

Department of Paediatric Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom.

出版信息

Front Neurol. 2020 Sep 16;11:954. doi: 10.3389/fneur.2020.00954. eCollection 2020.

Abstract

Third window disorders are structural abnormalities in the bony otic capsule that establish a connection between the middle/inner ear or the inner ear/cranial cavity. Investigated extensively in adults, they have hardly been studied in children. This study is a retrospective study of children (aged 5-17 years) diagnosed with rare third window disorders (third window disorders reported rarely or not reported in children) in a tertiary pediatric vestibular unit in the United Kingdom. It aimed to investigate audiovestibular function in these children. Final diagnosis was achieved by high resolution CT scan of the temporal bones. Of 920 children attending for audiovestibular assessment over a 42 month period, rare third windows were observed in 8 (<1%). These included posterior semicircular canal dehiscence ( = 3, 0.3%), posterior semicircular canal thinning ( = 2, 0.2%), X linked gusher ( = 2, 0.2%), and a combination of dilated internal auditory meatus/irregular cochlear partition/deficient facial nerve canal ( = 1, 0.1%). The majority of them (87.5%) demonstrated a mixed/conductive hearing loss with an air-bone gap in the presence of normal tympanometry (100%). Transient otoacoustic emissions were absent with a simultaneous cochlear pathology in 50% of the cohort. Features of disequilibrium were observed in 75% and about a third showed deranged vestibular function tests. Video head impulse test abnormalities were detected in 50% localizing to the side of the lesion. Cervical vestibular evoked myogenic potential test abnormalities were observed in all children in the cohort undergoing the test where low thresholds and high amplitudes classically found in third window disorders localized to the side of the defects in 28.5%. In the series, 71.4% also demonstrated absent responses/amplitude asymmetry, some of which did not localize to the ipsilesional side. Two children presented with typical third window symptoms. This study observes 2 new rare pediatric third window phenotypes and the presence of a cochlear hearing loss in these disorders. It emphasizes that these disorders should be considered as an etiology of hearing loss/disequilibrium in children. It also suggests that pediatric third window disorders may not present with classical third window features and are variable in their presentations/audiovestibular functions.

摘要

第三窗疾病是指在骨迷路囊中的结构异常,其在中耳/内耳或内耳/颅腔之间建立了连接。在成人中对其进行了广泛研究,但在儿童中几乎未被研究。本研究是一项对在英国一家三级儿科前庭单元被诊断为罕见第三窗疾病(在儿童中很少报道或未报道的第三窗疾病)的儿童(5 - 17岁)的回顾性研究。其目的是调查这些儿童的听前庭功能。通过颞骨高分辨率CT扫描做出最终诊断。在42个月期间接受听前庭评估的920名儿童中,发现8例(<1%)有罕见的第三窗疾病。这些包括后半规管裂开(n = 3,0.3%)、后半规管变薄(n = 2,0.2%)、X连锁性耳内积水(n = 2,0.2%)以及内耳道扩张/耳蜗分隔不规则/面神经管缺损的组合(n = 1,0.1%)。其中大多数(87.5%)表现为混合性/传导性听力损失,在鼓室图正常(100%)的情况下存在气骨导差。50%的队列同时存在耳蜗病变时瞬态耳声发射缺失。75%的儿童观察到失衡特征,约三分之一的儿童前庭功能测试异常。视频头脉冲测试异常在50%中被检测到,定位于病变侧。在接受测试的队列中的所有儿童中均观察到颈前庭诱发肌源性电位测试异常,其中28.5%的儿童具有第三窗疾病中典型的低阈值和高振幅,定位于缺损侧。在该系列中,71.4%的儿童也表现出反应缺失/振幅不对称,其中一些并非定位于患侧。两名儿童出现典型的第三窗症状。本研究观察到2种新的罕见儿童第三窗表型以及这些疾病中存在耳蜗性听力损失。它强调这些疾病应被视为儿童听力损失/失衡的病因。它还表明儿童第三窗疾病可能不会表现出典型的第三窗特征,并且其表现/听前庭功能存在差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c42/7526203/67f801f621e0/fneur-11-00954-g0001.jpg

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