Kawano T, Fukui M, Hashimoto N, Yonekawa Y
Department of Neurosurgery, Fukuoka Tokushukai Hospital.
Neurol Med Chir (Tokyo). 1994 Nov;34(11):744-7. doi: 10.2176/nmc.34.744.
Sixty-four patients with "unilateral" occlusive disease of the circle of Willis were studied to evaluate progression to bilateral disease. Seventeen patients developed bilateral lesions during a period of 1-7 years after the diagnosis of unilateral lesion. Most of these patients had ischemic attack as the initial episode and had repeated attacks before admission. Young children, mostly less than 10 years of age, tended to develop bilateral lesions within 1-2 years, but adults tended to have only a unilateral lesion. Children or young adults with unilateral occlusive lesion of the terminal portion of the internal carotid artery are likely to develop bilateral disease within 1-5 years.
对64例患有Willis环“单侧”闭塞性疾病的患者进行了研究,以评估其进展为双侧疾病的情况。17例患者在单侧病变诊断后的1至7年内出现了双侧病变。这些患者大多以缺血性发作作为首发症状,且在入院前有多次发作。年幼的儿童,大多小于10岁,倾向于在1至2年内发展为双侧病变,但成年人往往只有单侧病变。患有颈内动脉末端单侧闭塞性病变的儿童或年轻成年人很可能在1至5年内发展为双侧疾病。