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对侧椎动脉 parent 动脉闭塞后新发椎动脉夹层动脉瘤

De Novo Vertebral Artery Dissecting Aneurysm after Parent Artery Occlusion of the Contralateral Vertebral Artery.

作者信息

Tsuji Yuichiro, Murase Sho, Kuroda Yuzo, Wanibuchi Masahiko

机构信息

Department of Neurosurgery, Kano General Hospital, Osaka, Japan.

Department of Neurology, Kano General Hospital, Osaka, Japan.

出版信息

J Korean Neurosurg Soc. 2024 Jan;67(1):115-121. doi: 10.3340/jkns.2022.0263. Epub 2023 May 4.

Abstract

After treatment of unilateral vertebral artery dissecting aneurysm (VADA), de novo VADA rarely occurs on the contralateral side. In this article, we report a case of subarachnoid hemorrhage (SAH) due to de novo VADA in the contralateral vertebral artery (VA) 3 years after parent artery occlusion of unilateral VADA, with a review of the literature. A 47-year-old woman was admitted to our hospital complaining of headache and impaired consciousness. Head computed tomography showed SAH, and three-dimensional computed tomography angiography showed a fusiform aneurysm in the left VA. We performed an emergency parent artery occlusion. Three years and 3 months after the initial treatment, the patient presented to our hospital with complaints of headache and neck pain. Magnetic resonance imaging revealed SAH, and magnetic resonance angiography revealed de novo VADA in the right VA. We performed a stent-assisted coil embolization. The patient had a good postoperative course and was discharged with a modified Rankin scale score of 0. Long-term follow-up is necessary in patients with VADA because contralateral de novo VADA can develop even several years after the initial treatment.

摘要

单侧椎动脉夹层动脉瘤(VADA)治疗后,对侧很少发生新生VADA。在本文中,我们报告1例单侧VADA母动脉闭塞3年后对侧椎动脉(VA)发生新生VADA导致蛛网膜下腔出血(SAH)的病例,并进行文献复习。一名47岁女性因头痛和意识障碍入院。头部计算机断层扫描显示SAH,三维计算机断层扫描血管造影显示左椎动脉有一个梭形动脉瘤。我们进行了急诊母动脉闭塞术。初始治疗3年零3个月后,患者因头痛和颈部疼痛再次入院。磁共振成像显示SAH,磁共振血管造影显示右椎动脉有新生VADA。我们进行了支架辅助弹簧圈栓塞术。患者术后恢复良好,出院时改良Rankin量表评分为0分。VADA患者需要长期随访,因为即使在初始治疗数年之后,对侧也可能发生新生VADA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aee9/10788547/d2e242fbda14/jkns-2022-0263f1.jpg

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