中国卒中杂志 ›› 2024, Vol. 19 ›› Issue (4): 452-458.DOI: 10.3969/j.issn.1673-5765.2024.04.008

• 病例讨论 • 上一篇    下一篇

伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病患者大脑中动脉闭塞血管内治疗1例并文献复习

刘昱君,刘雷媛,徐炳东,韩建邦,杨冰,丁燕,杨英,孟珩,张玉生   

  1. 广州 510630 暨南大学附属第一医院神经内科
  • 收稿日期:2023-10-30 出版日期:2024-04-20 发布日期:2024-04-20
  • 通讯作者: 张玉生 757181750@qq.com
  • 基金资助:
    广东省自然科学基金面上项目(2020A1515011249)
    中央高校基本科研业务费专项基金(21620406)
    广州市科技计划项目(2023A03J0577)

Endovascular Treatment of Middle Cerebral Artery Occlusion in Patient with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: A Case Report and Literature Review

LIU Yujun, LIU Leiyuan, XU Bingdong, HAN Jianbang, YANG Bing, DING Yan, YANG Ying, MENG Heng, ZHANG Yusheng   

  1. Department of Neurology, The First Affiliated Hospital of Jinan University, Guangzhou 510630, China
  • Received:2023-10-30 Online:2024-04-20 Published:2024-04-20
  • Contact: ZHANG Yusheng, E-mail: 757181750@qq.com

摘要: 伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy,CADASIL)是NOTCH3基因突变所致的遗传性脑小血管病,主要病变血管为颅内小动脉,累及大脑皮质和颅内大/中动脉的报道较罕见,目前缺乏特效治疗方法。本文报道1例大脑中动脉急性闭塞成功接受血管内治疗的CADASIL病例,并结合文献进行讨论,旨在引起临床医师对CADASIL可累及大脑皮质和颅内大/中动脉的重视。

关键词: 伴皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病; 血管内治疗; 大脑中动脉

Abstract: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary cerebral small vessel disease caused by mutations in the NOTCH3 gene. The main vascular pathological changes in CADASIL are intracranial small arteries, with rare reports of involvement in the cerebral cortex and intracranial large/middle arteries. There is currently a lack of specific treatment for CADASIL. This paper reported a case of CADASIL patient who successfully received endovascular treatment for acute occlusion of middle cerebral artery, and discussed the literature with the aim of raising clinical awareness of the potential involvement of CADASIL in the cerebral cortex and intracranial large/middle arteries.

Key words: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; Endovascular treatment; Middle cerebral artery

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