双侧水平声道发育不良,表现为听力损失并伴有模仿梅尼埃病的复发性眩晕。

Wonyong Baek, Young Jae Lee, Gi-Sung Nam
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引用次数: 0

摘要

我们报告了一例极其罕见的病例,患者双侧水平半规管(HSC)发育不良,表现为听力损失并伴有反复眩晕,模仿美尼尔氏病,患者之前健康,现年 49 岁。水平半规管畸形是骨性迷宫常见的孤立发育异常之一,通常伴有不同程度的听力损失。他反复发作眩晕,持续时间超过 20 分钟,伴有左耳听力损失和耳鸣,已有 3 年之久。纯音测听显示左耳低频听力轻度至中度下降。双耳热量测试显示左侧耳道明显麻痹,但其他前庭测试正常。颞骨计算机断层扫描(CT)显示,左侧造血干细胞发育不良,缺乏与前庭扩大融合在一起的中央骨岛,右侧发育不良,最终诊断为双侧造血干细胞发育不良。梅尼埃病的反复眩晕发作和听力损失被怀疑是由随后的内淋巴水肿引起的,而内淋巴水肿可能是造血干细胞发育不良所致。
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Bilateral Horizontal Canal Dysplasia Presenting as Hearing Loss With Recurrent Vertigo Mimicking Meniere's Disease.

We report an extremely rare case with bilateral horizontal semicircular canal (HSC) dysplasia presenting as hearing loss with recurrent vertigo mimicking Meniere's disease in a previously healthy 49-year-old male patient. HSC malformation is one of the common isolated developmental anomalies of the bony labyrinth usually associated with varying degree of hearing loss. He suffered from recurrent episodes of vertigo lasting more than 20 minutes accompanied by left hearing loss and tinnitus for 3 years. Pure-tone audiometry revealed a mild to moderate hearing loss at low frequencies in the left ear. Bithermal caloric testing revealed significant left-sided canal paralysis, but other vestibular testing was normal. Computerized tomography (CT) of the temporal bone showed the left HSC hypoplasia lacking a central bony island fused together with an enlarged vestibule, and right dysplasia, finally diagnosed with bilateral HSC dysplasia. Meniere's disease-like recurrent vertigo attack and hearing loss were suspected to be caused by subsequent endolymphatic hydrops which could be due to HSC dysplasia.

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