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[半规管裂综合征]

[Semicircular canal dehiscence syndrome].

作者信息

Garner Malvina

机构信息

Klinik für diagnostische und interventionelle Neuroradiologie, Universitätskliniken des Saarlandes, Kirrberger Str., 66421, Homburg Saar, Deutschland.

出版信息

Radiologie (Heidelb). 2025 Aug;65(8):595-600. doi: 10.1007/s00117-025-01468-4. Epub 2025 Jun 23.

Abstract

Semicircular canal dehiscence (SCD) is a rare but clinically significant cause of vertigo and auditory symptoms. The clinical presentation is relatively specific and typically includes sound- or pressure-induced rotational vertigo accompanied by nystagmus, autophony, hypersensitivity to bone-conducted sound (hyperacusis), and pseudo-conductive hearing loss. Imaging plays a central role in establishing an accurate diagnosis and in excluding differential diagnoses. High-resolution thin-slice computed tomography (CT), particularly when combined with magnetic resonance imaging (MRI), forms the cornerstone of radiologic assessment. Importantly, a substantial proportion of patients with radiologically confirmed dehiscence remain asymptomatic. While the presence of vestibular symptoms in conjunction with a bony dehiscence should raise suspicion for SCD syndrome, other etiologies must be prioritized in the differential diagnosis based on clinical history, examination, and imaging findings, given the rarity of the condition.

摘要

半规管裂(SCD)是导致眩晕和听觉症状的一种罕见但具有临床意义的病因。其临床表现相对具有特异性,通常包括声音或压力诱发的旋转性眩晕并伴有眼球震颤、自听过强、对骨导声音过敏(听觉过敏)以及假性传导性听力损失。影像学检查在准确诊断和排除鉴别诊断方面起着核心作用。高分辨率薄层计算机断层扫描(CT),尤其是与磁共振成像(MRI)相结合时,构成了放射学评估的基石。重要的是,相当一部分经放射学证实存在裂的患者并无症状。虽然前庭症状与骨质裂同时出现应引起对SCD综合征的怀疑,但鉴于该病症较为罕见,在基于临床病史、检查和影像学表现进行鉴别诊断时,必须优先考虑其他病因。

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