{"title":"Bow hunter syndrome","authors":"A. Kühn, G. Mcgillicuddy, Jasmeet Singh","doi":"10.1097/01.cne.0000446651.48346.7a","DOIUrl":null,"url":null,"abstract":"CMAJ | November 7, 2022 | Volume 194 | Issue 43 © 2022 CMA Impact Inc. or its licensors A 59-year-old man presented to our neuroendovascular clinic with a 10-month history of chronic dizziness, described as a spinning sensation, with associated gait instability and blurred vision upon head rotation. On examination, the spinning sensation could be elicited with mostly leftward head rotation. When the patient turned his head to a more neutral position, the symptoms slowly subsided. Flexion or extension of the neck did not elicit vertigo. The Dix–Hallpike manoeuvre did not elicit nystagmus and a Romberg test was negative. We did not observe any other neurologic abnormalities. We initially thought the patient had benign paroxysmal positional vertigo; however, the Epley manoeuvres, vestibular rehabilitation therapy and meclizine were ineffective. Given the refractory nature of the patient’s vertigo, lack of a clear diagnosis and persistent ability to elicit symptoms with head rotation, we ordered cerebral angiography, which showed focal 80% narrowing of the left vertebral artery with a leftward head turn (Figure 1). We diagnosed bow hunter syndrome (BHS) and referred the patient to a neuro surgeon for an anterior cervical discectomy and removal of the uncinate process and associated osteophyte, which was compressing the left vertebral artery. At 3 months postsurgery, the patient described no rotational vertigo with only residual dizziness, which was gradually improving. Bow hunter syndrome is also called rotational vertebral artery occlusion syndrome.1,2 Patients usually present with reproducible, transient vertigo when they rotate or extend their head owing to dynamic stenosis of the affected vertebral artery (most often caused by an osteophyte, less often by disc herniations or tumours).2 The incidence of BHS is not known and there are no guidelines on diagnosis and management. Imaging to diagnose BHS includes computed tomography angiography, magnetic resonance angiography and cerebral angiography.1,3 Some patients can be managed nonoperatively, whereas others benefit from surgery, which appears to have a good prognosis.3","PeriodicalId":10359,"journal":{"name":"CMAJ : Canadian Medical Association Journal","volume":"52 1","pages":"E1486 - E1486"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CMAJ : Canadian Medical Association Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/01.cne.0000446651.48346.7a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
弓猎人综合症
CMAJ | 2022年11月7日|卷194 |第43期©2022 CMA Impact Inc.或其许可方一名59岁男性,因10个月的慢性头晕病史来到我们的神经血管内诊所,描述为旋转感,伴有步态不稳定和头部旋转时视力模糊。在检查中,旋转感觉主要是由头部向左旋转引起的。当病人把头转到一个更中立的位置时,症状慢慢消退。颈部的屈曲或伸展不会引起眩晕。迪克斯-霍尔派克运动没有引起眼球震颤,Romberg试验为阴性。我们未观察到任何其他神经系统异常。我们最初认为患者是良性阵发性位置性眩晕;然而,Epley手法、前庭康复治疗和美唑嗪均无效。考虑到患者眩晕的难治性,缺乏明确的诊断和持续引起头部旋转症状的能力,我们进行了脑血管造影,结果显示左侧椎动脉局灶性狭窄80%,伴有头部向左转动(图1)。我们诊断为弓形猎人综合征(BHS),并将患者转至神经外科医生行颈椎前路椎间盘切除术,去除钩突和相关骨赘。压迫了左椎动脉。术后3个月,患者无旋转性眩晕,仅残留头晕,并逐渐改善。弓猎人综合征也称为旋转椎动脉闭塞综合征。1,2由于受影响的椎动脉动态狭窄,患者在旋转或伸展头部时通常表现为可重复的短暂性眩晕(最常由骨赘引起,较少由椎间盘突出或肿瘤引起)BHS的发病率尚不清楚,也没有诊断和管理指南。诊断BHS的影像学包括计算机断层血管造影、磁共振血管造影和脑血管造影。一些患者可以非手术治疗,而另一些患者则受益于手术,手术预后良好
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