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弓猎者卒中中滑膜囊肿所致椎动脉夹层:病例报告

A synovial cyst-induced vertebral artery dissection in bow hunter's stroke: illustrative case.

作者信息

Yamashita Masahito, Hayashi Hideki, Kitamura Kazushi, Ishibashi Ryota, Toda Hiroki

机构信息

Department of Neurosurgery, Tazuke Kofukai Medical Research Institute, Kitano Hospital, Osaka, Japan.

出版信息

J Neurosurg Case Lessons. 2024 Aug 12;8(7). doi: 10.3171/CASE2487.

Abstract

BACKGROUND

Bow hunter's stroke (BHS) is a rare condition characterized by occlusion of the vertebral artery (VA) due to a head rotation. BHS typically results from neck hyperrotation, often due to anatomical factors. The authors present a case of BHS in a young male patient exacerbated by os odontoideum (OD), resulting in atlantoaxial dislocation, which ultimately led to VA dissection.

OBSERVATIONS

A man in his 20s presented with persistent dizziness and nausea and initially received a diagnosis of a brain infarction. However, imaging revealed VA dissection caused by an OD with an associated synovial cyst. Surgical intervention, specifically atlantoaxial posterior fixation, resolved the instability and allowed for natural regression of the synovial cysts, preventing further vascular events. In this case, the OD with atlantoaxial dislocation was identified as the causative factor for BHS. The coexistence of a synovial cyst was a unique finding, likely triggered by chronic irritation caused by the OD.

LESSONS

This case emphasizes the importance of thorough cervical spinal evaluation in young patients presenting with posterior circulation stroke. https://thejns.org/doi/10.3171/CASE2487.

摘要

背景

弓猎者卒中(BHS)是一种罕见疾病,其特征为因头部旋转导致椎动脉(VA)闭塞。BHS通常由颈部过度旋转引起,常因解剖学因素所致。作者报告一例年轻男性患者的BHS,因齿突骨(OD)而加重,导致寰枢椎脱位,最终引发椎动脉夹层。

观察结果

一名20多岁男性出现持续性头晕和恶心,最初被诊断为脑梗死。然而,影像学检查显示由OD伴滑膜囊肿引起的椎动脉夹层。手术干预,特别是寰枢椎后路固定,解决了不稳定问题,并使滑膜囊肿自然消退,防止了进一步的血管事件。在本病例中,伴有寰枢椎脱位的OD被确定为BHS的致病因素。滑膜囊肿的并存是一个独特发现,可能由OD引起的慢性刺激触发。

经验教训

本病例强调了对出现后循环卒中的年轻患者进行全面颈椎评估的重要性。https://thejns.org/doi/10.3171/CASE2487

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e75/11323843/07a77fdeff28/CASE2487_figure_1.jpg

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