Brantberg Krister, Greitz Dan, Pansell Tony
Departments of Audiology, Karolinska Hospital, St. Eriks Eye Hospital, Stockholm, Sweden.
Otol Neurotol. 2004 Nov;25(6):993-7. doi: 10.1097/00129492-200411000-00022.
To present a patient with symptoms similar to those of superior canal dehiscence syndrome due to another cause.
Case report.
University hospital, tertiary referral center.
The 65-year-old woman had suffered for 4 years from hearing loss, tinnitus, and pressure-induced vertigo.
Audio-vestibular testing, high-resolution computed tomography, and magnetic resonance angiography.
The superior canal dehiscence syndrome is caused by failure of normal postnatal bone development in the middle cranial fossa leading to absence of bone at the most superior part of the superior semicircular canal. The typical features for this syndrome are sound and pressure-induced vertigo with torsional eye movements, pulse synchronous tinnitus and apparent conductive hearing loss in spite of normal middle ear function. We present a patient with very similar symptoms and findings, who instead had a superior canal dehiscence close to the common crus. Neuroradiologic findings suggested that the dehiscence was related to a venous malformation.
Symptoms and findings suggesting superior canal dehiscence syndrome can have a different cause.
报告一名因其他病因出现类似半规管裂综合征症状的患者。
病例报告。
大学医院,三级转诊中心。
一名65岁女性,听力损失、耳鸣和压力性眩晕4年。
听-前庭测试、高分辨率计算机断层扫描和磁共振血管造影。
半规管裂综合征是由中颅窝出生后正常骨发育失败导致上半规管最上部无骨质引起的。该综合征的典型特征是声音和压力诱发的眩晕伴眼球扭转运动、脉搏同步性耳鸣以及尽管中耳功能正常但明显的传导性听力损失。我们报告一名有非常相似症状和检查结果的患者,其在靠近总脚处存在半规管裂。神经放射学检查结果提示该裂与静脉畸形有关。
提示半规管裂综合征的症状和检查结果可能有不同病因。