唐氏综合征患者前庭导水管增大及其他内耳异常

C. Clark, Hetal H. Patel, S. Kanekar, Huseyin Isildak
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引用次数: 13

摘要

背景:唐氏综合征患者内耳结构的组织病理学异常已经有了很好的记录;然而,很少有研究检查放射学特征。方法:回顾性研究38例(75耳)唐氏综合征患者颞骨ct图像,评估内耳异常的患病率和前庭导尿管宽度。结果:38例患者中有20例(52.6%)出现内耳异常。在75块颞骨中,有7块(9.3%)的骨密度比先前报道的要高。在本研究组中,内耳道和前庭扩张更为常见,而先前的研究表明内耳道狭窄和前庭缩小。结论:唐氏综合征患者表现出高度普遍的内耳发育不良特征,这赋予了感觉神经性听力损失的巨大风险。计算机断层扫描是检测内耳异常的有用筛查手段,特别是前庭导尿管扩大,这在该人群中引起可预防的感音神经性听力损失。
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Enlarged vestibular aqueducts and other inner-ear abnormalities in patients with Down syndrome
Abstract Background: Histopathological anomalies of inner-ear structures in individuals with Down syndrome have been well documented; however, few studies have examined the radiological features. Methods: A retrospective study was conducted of temporal bone computed tomography images in 38 individuals (75 ears) with Down syndrome to evaluate the prevalence of inner-ear abnormalities and assess vestibular aqueduct widths. Results: Inner-ear anomalies were identified in 20 of the 38 individuals (52.6 per cent). Seven of the 75 temporal bones (9.3 per cent) were found to have higher than previously reported. A dilated internal auditory canal and vestibule were more common among the present study group, while prior studies have demonstrated internal auditory canal stenosis and decreased vestibule size. Conclusion: Down syndrome patients exhibit a high prevalence of dysplastic inner-ear features that confer substantial risk of sensorineural hearing loss. Computed tomography is a useful screening aid to detect inner-ear abnormalities, particularly enlarged vestibular aqueducts, which cause preventable sensorineural hearing loss in this population.
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