一例特殊的听力损失,多年后伴有耳鸣和眩晕

V. Marcelli, M. Cavaliere, M. Mesolella, E. Cantone, A. M. D. Lullo, Carla Laria, P. Apisa, Rita Malesci, E. Bernardo, F. Ricciardiello, Elisabetta Cristiano, Salvatore Mazzone, C. Tripodi, A. Marzetti, G. Auletta, G. Tortoriello
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引用次数: 0

摘要

前庭发作(也称为致残性位置性眩晕)是一种由第八颅神经的症状性神经血管压迫引起的临床综合征。尽管一些作者对此表示怀疑,但必须怀疑存在短暂的位置前庭症状,这些症状与暂时或永久但恶化的耳蜗前庭症状和体征有关,而其他疾病无法解释这一点。我们报告了一例20岁女孩的病例,她从4-5岁起就患有永久性右耳感音神经性听力损失,随后右耳出现间歇性低频耳鸣,并因体位或身体活动而出现眩晕或眩晕。大脑的血管造影MRI显示右侧椎动脉和右侧第八颅神经之间有一个独特的神经血管接触。对卡马西平的良好反应证实了该综合征的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A peculiar case of hearing loss followed years later by tinnitus and vertigo
Vestibular paroxysmia (also known as disabling positional vertigo) is a clinical syndrome generated by a symptomatic neurovascular compression of the eighth cranial nerve. Although doubted by some authors, this syndrome must be suspected in presence of brief spells of positional vestibular symptoms associated with temporary or permanent but worsening cochlea-vestibular symptoms and signs, not explained by other diseases. We report a case of a 20-year-old girl affected by permanent sensorineural hearing loss on the right since the age of 4-5 years, who subsequently developed intermittent low pitch tinnitus on the right ear and spells of vertigo or dizziness generated by position or physical activity. Angio-MRI of the brain showed a singular neurovascular contact between the right vertebral artery and the right eighth cranial nerve. The excellent response to carbamazepine confirms the presence of this syndrome.
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