Chuang Yu-Ming, Liu Chih-Yang, Pan Po-Jung, Lin Ching-Po
Department of Neurology, Tao-Yuan General Hospital, Tao-Yuan City, Taiwan, ROC.
Eur Neurol. 2007;57(4):208-11. doi: 10.1159/000099160. Epub 2007 Jan 19.
Anterior cerebral artery A1 segment hypoplasia is an uncommon fetal variant of the circle of Willis. The frequency of this congenital variation is 1-13% as derived from angiograms and autopsy reports. Impaired collateral blood flow through the circle of Willis is a recognized risk factor for ischemic stroke. The A1 segment of the anterior cerebral artery is a principal supplier of anterior collateral blood flow. The aim of our study was to determine whether A1 segment hypoplasia may be responsible for acute ischemic stroke. We consecutively examined 280 acute ischemic stroke patients (aged 66.9 +/- 14.2 years). Cerebral magnetic resonance angiography was performed within 72 h of ischemic stroke onset. The overall incidence of A1 variation in our experimental group was 15.0% (n = 42, agenesis/hypoplasia = 18/24), which was statistically higher than in the control group (n = 12). The majority (n = 30, 71.42%) had ipsilateral striatal lacunar infarctions. Based on our results, A1 agenesis/hypoplasia appears to be a risk factor contributing to ischemic stroke, especially to strokes in arteries penetrating the striatal area.
大脑前动脉A1段发育不全是一种罕见的Willis环胎儿变异。根据血管造影和尸检报告,这种先天性变异的发生率为1% - 13%。通过Willis环的侧支血流受损是缺血性中风公认的危险因素。大脑前动脉A1段是前侧支血流的主要供应者。我们研究的目的是确定A1段发育不全是否可能导致急性缺血性中风。我们连续检查了280例急性缺血性中风患者(年龄66.9±14.2岁)。在缺血性中风发作72小时内进行了脑磁共振血管造影。我们实验组中A1变异的总发生率为15.0%(n = 42,缺如/发育不全 = 18/24),在统计学上高于对照组(n = 12)。大多数(n = 30,71.42%)有同侧纹状体腔隙性梗死。根据我们的结果,A1段缺如/发育不全似乎是导致缺血性中风的一个危险因素,尤其是累及穿透纹状体区域动脉的中风。