Podwall Arthur, Podwall David, Gordon Toni G, Lamendola Paula, Gold Arnold P
Syosset Speech & Hearing Center, New York 11791, USA.
J Child Neurol. 2002 Apr;17(4):306-9. doi: 10.1177/088307380201700415.
This article reports on an 11-year-old boy who was diagnosed with unilateral auditory neuropathy. After failing his annual medical and school hearing screenings, he was referred for audiologic testing, which identified a profound sensorineural hearing loss in his left ear that has remained stable for the past 3 1/2 years. Subsequently, otoacoustic emissions revealed findings that were consistent with an auditory neuropathy. Neurologic evaluation was remarkable only for a left ear hearing loss. Radiologic studies were unremarkable. Auditory neuropathy is a condition in which patients, on audiologic evaluation, are found to have normal outer hair cell function and abnormal neural function at the level of the eighth nerve. These patients, on clinical testing, are found to have normal otoacoustic emissions, whereas auditory brainstem response audiometry reveals the absence of neural synchrony. Unlike space-occupying lesions, radiologic evaluation reveals normal results. This case is noteworthy because only a handful of the cases of auditory neuropathy reported to date have been unilateral.
本文报道了一名11岁男孩,他被诊断为单侧听觉神经病。在年度医学和学校听力筛查未通过后,他被转介进行听力学测试,结果发现他左耳存在严重的感音神经性听力损失,且在过去3年半中一直保持稳定。随后,耳声发射显示的结果与听觉神经病相符。神经学评估仅显示左耳听力损失较为明显。放射学检查未见异常。听觉神经病是一种在听力学评估中发现患者外毛细胞功能正常但第八神经水平神经功能异常的病症。这些患者在临床测试中,耳声发射正常,而听觉脑干反应测听显示神经同步性缺失。与占位性病变不同,放射学评估结果正常。该病例值得关注,因为迄今为止报告的听觉神经病病例中只有少数是单侧的。