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伴有咔哒声的弓猎综合征:一种伴有强直阵挛性发作的短暂意识丧失的罕见病因。

Bow Hunter's syndrome with clicking sounds: A rare etiology of transient loss of consciousness with tonic-clonic seizure.

作者信息

Wang Lijuan, Dong Yanan, Chen Hongxiu, Bai Jing, Zhu Mingqin, Xing Yingqi

机构信息

Department of Neurology, The First Hospital of Jilin University, Changchun, China.

Department of Vascular Ultrasonography, Xuanwu Hospital Capital Medical University, Beijing, China.

出版信息

Front Neurol. 2023 Jan 12;13:1088842. doi: 10.3389/fneur.2022.1088842. eCollection 2022.

Abstract

We present the case of a young male patient experiencing a transient loss of consciousness and manifesting a seizure when he tilted his head backward. Transcranial Doppler ultrasound (TCD) and carotid artery ultrasound (CAU) examination were normal when the patient's neck was in the neutral position. However, the CAU revealed vertebral artery (VA) transient occlusion during neck rotation or backward movement. Electroencephalogram (EEG) monitoring was performed with multiple neck rotation-induced tests. The patient developed dizziness, which was the same as the prodromal symptoms of the first seizure, and the EEG showed a large number of spinal slow waves and sharp slow waves in the frontal-to-frontal midline area, with an occasional generalization trend. CT angiography revealed occipitalization of the atlas and the lack of contrast agent filling in the local area of the VA when the patient's head was turned contralaterally. Thus, the patient was diagnosed with Bow Hunter's syndrome (BHS) and treated conservatively with neck immobilization. No recurrence occurred at 3 and 6 months of follow-up. Therefore, this case alerts neurologists to suspect BHS on observing seizure manifestations during neck rotation, and CAU may be a recommended dynamic screening method for BHS. This report is accompanied by a discussion of the phenomenon and diagnosis in the context of the existing literature.

摘要

我们报告一例年轻男性患者,该患者在向后仰头时出现短暂意识丧失并伴有癫痫发作。当患者颈部处于中立位时,经颅多普勒超声(TCD)和颈动脉超声(CAU)检查结果正常。然而,CAU显示在颈部旋转或向后移动时椎动脉(VA)出现短暂闭塞。通过多次颈部旋转诱发试验进行脑电图(EEG)监测。患者出现头晕,与首次癫痫发作的前驱症状相同,EEG显示额部至额中线区域出现大量脊髓慢波和尖慢波,偶尔有泛化趋势。CT血管造影显示当患者头部向对侧转动时,寰椎枕化且VA局部区域无造影剂充盈。因此,该患者被诊断为Bow Hunter综合征(BHS),并采用颈部固定进行保守治疗。随访3个月和6个月时均未复发。因此,该病例提醒神经科医生,在观察到颈部旋转时出现癫痫发作表现时要怀疑BHS,CAU可能是推荐用于BHS的动态筛查方法。本报告还结合现有文献对该现象及诊断进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aded/9878292/4f12c7668cb5/fneur-13-1088842-g0001.jpg

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