Rafay Mubeen F, Armstrong Derek, Deveber Gabrielle, Domi Trish, Chan Anthony, MacGregor Daune L
Division of Neurology, The Hospital for Sick Children, Toronto, ON, Canada.
J Child Neurol. 2006 Jan;21(1):8-16. doi: 10.1177/08830738060210010101.
Craniocervical arterial dissection is a recognized cause of arterial ischemic stroke in children. Whether children with craniocervical arterial dissection have dissection characteristics different from those of adults is unclear. A retrospective review of children, 1 month to 18 years of age, with dissection from two Canadian pediatric ischemic stroke registry centers was conducted. From 213 patients with arterial ischemic stroke, 16 (7.5%) were identified with dissection, 37.5% had warning symptoms, and 50% had a history of head or neck trauma. The clinical presentation included headache (44%), altered consciousness (25%), seizures (12.5%), and focal deficits (87.5%). Dissection involved extracranial vessels in 75% and anterior circulation in 56%. Follow-up included complete recovery in 43%, mild to moderate deficits in 44%, and severe deficits in 13%. Fourteen (87.5%) children received antithrombotic treatment. Follow-up angiography showed resolution of abnormalities in 60% of vessels. Total occlusion had the worst outcome for recanalization. In conclusion, the etiology of arterial dissection in the majority of children appears to be either trauma or idiopathic. Long-term angiography shows variable outcomes, depending on the initial findings. The relationship of angiographic outcomes with recurrent strokes requires further study in pediatric dissection. (J Child Neurol 2006;21:8-16).
颅颈动脉夹层是儿童动脉缺血性卒中的一个公认病因。颅颈动脉夹层患儿是否具有与成人不同的夹层特征尚不清楚。对来自两个加拿大儿科缺血性卒中登记中心的1个月至18岁患有夹层的儿童进行了回顾性研究。在213例动脉缺血性卒中患者中,16例(7.5%)被确诊为夹层,37.5%有预警症状,50%有头颈部外伤史。临床表现包括头痛(44%)、意识改变(25%)、癫痫发作(12.5%)和局灶性神经功能缺损(87.5%)。75%的夹层累及颅外血管,56%累及前循环。随访结果显示,43%完全恢复,44%有轻至中度神经功能缺损,13%有严重神经功能缺损。14例(87.5%)儿童接受了抗栓治疗。随访血管造影显示60%的血管异常消失。完全闭塞的血管再通预后最差。总之,大多数儿童动脉夹层的病因似乎是外伤或特发性。长期血管造影显示预后各异,取决于初始检查结果。血管造影结果与复发性卒中的关系需要在儿科夹层中进一步研究。(《儿童神经病学杂志》2006年;21:8 - 16)