Sheykholeslami Kianoush, Schmerber Sébastien, Habiby Kermany Mohammad, Kaga Kimitaka
Department of Otolaryngology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Acta Otolaryngol. 2005 Jul;125(7):786-91. doi: 10.1080/00016480510029284.
In a patient with bilateral auditory neuropathy (AN), the vestibular-evoked myogenic potential (VEMP) was probably absent because of a neuropathy involving the inferior vestibular nerve and/or its end organ, the saccule. Our result can therefore be interpreted as a concomitant unilateral sacculo-collic neuropathy. We suggest the use of more precise terms to characterize AN patients with involvement of different parts of the inner ear and its innervations. We encourage detailed vestibular assessment in patients with AN in order to assess the co-existence of any symptomatic or asymptomatic vestibular disorder. Information such as that provided in this report will be valuable for clinicians caring for this group of patients.
AN is a disorder characterized by the absence or severe impairment of auditory brainstem responses in the presence of normal cochlear outer hair cell function as revealed by otoacoustic emissions (OAEs) and/or electrocochleography (ECoG). A variety of processes and etiologies are thought to be involved in its pathophysiology. In most literature reports the auditory profile of patients with AN is discussed. However, the extent of vestibular involvement, especially that involving the saccule, is not known. We performed vestibular tests to assess the status of the saccule in a patient with AN.
One patient with AN was studied. The patient was a right-handed 21-year-old female with chief complaints of hearing loss and speech perception difficulty.
The auditory test results were consistent with the diagnosis of AN, i.e. absent auditory brainstem responses, moderate hearing loss, an inappropriately profound speech discrimination score and the presence of OAEs and measurable cochlear microphonics on ECoG. On neurological examination, gait and balance tests were normal. Ice-water caloric testing induced a sensation of dizziness in both ears. Short tone-burst VEMPs showed no response on left-ear stimulation and a biphasic response with normal latency and amplitude on right-ear stimulation.
在一名双侧听觉神经病(AN)患者中,前庭诱发肌源性电位(VEMP)可能缺失,这是由于涉及下前庭神经和/或其终器球囊的神经病变所致。因此,我们的结果可解释为伴有单侧球囊 - 颈神经病变。我们建议使用更精确的术语来描述内耳及其神经支配不同部位受累的AN患者。我们鼓励对AN患者进行详细的前庭评估,以评估任何有症状或无症状的前庭疾病的共存情况。本报告提供的此类信息对照顾这组患者的临床医生将很有价值。
AN是一种在耳声发射(OAEs)和/或耳蜗电图(ECoG)显示耳蜗外毛细胞功能正常的情况下,听觉脑干反应缺失或严重受损的疾病。其病理生理学被认为涉及多种过程和病因。在大多数文献报告中,讨论的是AN患者的听觉特征。然而,前庭受累的程度,尤其是涉及球囊的程度尚不清楚。我们进行了前庭测试以评估一名AN患者的球囊状态。
研究了一名AN患者。该患者为21岁右利手女性,主要症状为听力损失和言语感知困难。
听觉测试结果与AN的诊断一致,即听觉脑干反应缺失、中度听力损失、言语辨别得分异常低以及存在OAEs且ECoG上可测量到耳蜗微音电位。神经系统检查中,步态和平衡测试正常。冷热水试验双耳均诱发头晕感。短纯音VEMP在左耳刺激时无反应,在右耳刺激时出现潜伏期和振幅正常的双相反应。