Chief Neurosurgeon, Neuron Hospital, Vadodara, India.
Br J Neurosurg. 2023 Aug;37(4):808-810. doi: 10.1080/02688697.2019.1668538. Epub 2019 Sep 22.
Bow Hunter's syndrome is a rare disorder usually producing transient ischemic symptoms as a result of dynamic compression of the vertebral artery during head turning. We report a case of a 14 year old male presenting with stroke due to occlusion of vertebral artery due to rotatory atlanto-axial subluxation. The patient presented with sudden onset vertigo and ataxia. History revealed led mild torticollis since childhood which was never investigated. MRI and MRA showed infarcts in the bilateral cerebellar hemispheres and the occipital lobes with a hypoplastic left vertebral artery and kinking of the right vertebral artery at the cranio-vertebral junction due to rotatory atlanto-axial subluxation. The patient was successfully treated by C1 lateral mass and C2 sub-facetal screw with rod fixation. Bow-Hunter's syndrome producing transient ischemia is well reported but stroke in the vertebro-basilar territory in a 14 year old due to rotatory atlanto-axial subluxation is uncommon, and to the best of our knowledge, this is the eighth such reported case.
弓型 hunter 综合征是一种罕见的疾病,通常由于头部转动时椎动脉受到动态压迫而导致短暂性缺血症状。我们报告了一例 14 岁男性病例,因旋转性寰枢关节半脱位导致椎动脉闭塞而发生卒中。患者突发眩晕和共济失调。病史显示自幼轻度斜颈,从未进行过调查。MRI 和 MRA 显示双侧小脑半球和枕叶梗死,左侧椎动脉发育不良,右侧椎动脉在颅颈交界处因旋转性寰枢关节半脱位而扭曲。患者经 C1 侧块和 C2 下关节突螺钉棒固定成功治疗。弓型 hunter 综合征引起短暂性缺血已有充分报道,但 14 岁儿童因旋转性寰枢关节半脱位导致椎基底动脉区域卒中并不常见,据我们所知,这是第八例此类报道病例。