1Center for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women's Hospital.
2Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital.
J Neurosurg. 2017 Dec;127(6):1268-1276. doi: 10.3171/2016.9.JNS16503. Epub 2017 Jan 13.
Superior semicircular canal dehiscence (SSCD) syndrome is an increasingly recognized cause of vestibular and/or auditory symptoms in both adults and children. These symptoms are believed to result from the presence of a pathological mobile "third window" into the labyrinth due to deficiency in the osseous shell, leading to inadvertent hydroacoustic transmissions through the cochlea and labyrinth. The most common bony defect of the superior canal is found over the arcuate eminence, with rare cases involving the posteromedial limb of the superior canal associated with the superior petrosal sinus. Operative intervention is indicated for intractable or debilitating symptoms that persist despite conservative management and vestibular sedation. Surgical repair can be accomplished by reconstruction or plugging of the bony defect or reinforcement of the round window through a variety of operative approaches. The authors review the etiology, pathophysiology, presentation, diagnosis, surgical options, and outcomes in the treatment of this entity, with a focus on potential pitfalls that may be encountered during clinical management.
上半规管裂(SSCD)综合征是成人和儿童前庭和/或听觉症状日益被认识的原因。这些症状被认为是由于骨壳的缺陷导致病理性可动“第三窗口”进入迷路,从而导致耳蜗和迷路的无意中水声学传输。最常见的上半规管骨缺损位于弓状隆起上方,罕见情况下涉及上半规管后内侧支与岩上窦相关。对于持续存在的难治性或使人虚弱的症状,尽管进行了保守治疗和前庭镇静,仍需要手术干预。手术修复可以通过重建或阻塞骨缺陷或通过各种手术方法加强圆窗来完成。作者回顾了该实体的病因、病理生理学、表现、诊断、手术选择和治疗结果,重点介绍了在临床管理中可能遇到的潜在陷阱。