Wackym P Ashley, Wood Scott J, Siker David A, Carter Dale M
Ear and Skull Base Center, 1225 NE 2nd Ave., Suite 305, Portland, OR 97232, USA.
Ear Nose Throat J. 2015 Aug;94(8):E8-E24. doi: 10.1177/014556131509400802.
We conducted a prospective longitudinal study of two cohorts of patients who had superior semicircular canal dehiscence syndrome (SSCDS); one group had radiographically confirmed superior canal dehiscence (SCD), and the other exhibited no identified otic capsule dehiscence on imaging (no-iOCD). We compiled data obtained from prospective structured symptomatology interviews; diagnostic studies; three-dimensional, high-resolution, temporal bone computed tomography; and a retrospective case review from our tertiary care referral center. Eleven adults and 1 child with SSCDS were identified, surgically managed, and followed. Six of these patients-1 man and 5 women, aged 29 to 54 years at first surgery (mean: 41.8)-had radiologically confirmed SCD. The other 6 patients-1 man, 4 women, and 1 girl, aged 1 to 51 years (mean: 32.2)-had no-iOCD. The 6 adults with SCD underwent surgery via a middle cranial fossa approach with plugging procedures. The 5 adults and 1 child with no-iOCD underwent round window reinforcement (RWR) surgery. One SCD patient developed no-iOCD 1.5 years after SCD surgery, and she subsequently underwent RWR surgery. Our main outcome measures were patient symptomatology (with video documentation) and the results of diagnostic studies. Other than the character of migraine headaches, there was no difference in preoperative symptomatology between the two groups. Postoperatively, resolution of SSCDS symptoms ultimately occurred in all patients. Both the SCD and the no-iOCD groups experienced a highly significant improvement in postural control following treatment (Wilcoxon signed rank test, p < 0.001). We conclude that the term otic capsule dehiscence syndrome more accurately reflects the clinical syndrome of SSCDS since it includes both superior semicircular canal dehiscence and no-iOCD, as well as posterior and lateral semicircular canal dehiscence, all of which can manifest as SSCDS. We have also included links to videos in which 4 of the SSCDS patients with no-iOCD in this study discussed their symptoms and the results of their surgery; these links are found in the "References" section in citations 12-15. Links to three other videos of interest are contained in citations 10, 11, and 24.
我们对两组患有上半规管裂综合征(SSCDS)的患者进行了一项前瞻性纵向研究;一组经影像学证实存在上半规管裂(SCD),另一组在影像学上未发现内耳囊裂(无内耳囊裂,no - iOCD)。我们收集了从前瞻性结构化症状访谈、诊断研究、三维高分辨率颞骨计算机断层扫描以及我们三级医疗转诊中心的回顾性病例审查中获得的数据。共识别出11名成人和1名患有SSCDS的儿童,对他们进行了手术治疗并进行随访。其中6例患者(1名男性和5名女性,首次手术时年龄为29至54岁,平均41.8岁)经影像学证实存在SCD。另外6例患者(1名男性、4名女性和1名女孩,年龄为1至51岁,平均32.2岁)为无内耳囊裂。6例患有SCD的成人通过中颅窝入路并采用填塞手术进行治疗。5例成人和1名儿童无内耳囊裂患者接受了圆窗加固(RWR)手术。1例SCD患者在SCD手术后1.5年出现无内耳囊裂,随后接受了RWR手术。我们的主要结局指标是患者症状(有视频记录)和诊断研究结果。除偏头痛头痛的特征外,两组术前症状无差异。术后,所有患者的SSCDS症状最终均得到缓解。SCD组和无内耳囊裂组在治疗后姿势控制方面均有高度显著改善(Wilcoxon符号秩检验,p < 0.001)。我们得出结论,内耳囊裂综合征这一术语更准确地反映了SSCDS的临床综合征,因为它包括上半规管裂和无内耳囊裂,以及后半规管裂和外半规管裂,所有这些都可表现为SSCDS。我们还提供了视频链接,本研究中4例无内耳囊裂的SSCDS患者在视频中讨论了他们的症状和手术结果;这些链接在参考文献部分的引用12 - 15中。引用10、11和24中包含另外三个相关视频的链接。