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类风湿关节炎患者颅内和颅外多发性动脉夹层动脉瘤:一例报告。

Intracranial and extracranial multiple arterial dissecting aneurysms in rheumatoid arthritis: A case report.

机构信息

Department of Neurosurgery, Kumamoto University Hospital, Kumamoto, Japan.

Department of Cerebrovascular Medicine & Surgery, Division of Neurosurgery, Saiseikai Kumamoto Hospital, Kumamoto, Japan.

出版信息

Interv Neuroradiol. 2021 Apr;27(2):212-218. doi: 10.1177/1591019920965359. Epub 2020 Oct 20.

Abstract

OBJECTIVE

We describe a case of intracranial and extracranial multiple arterial dissecting aneurysms in rheumatoid arthritis (RA).

CASE PRESENTATION

A 29-year-old man with a medical history of RA since 18 years of age was admitted to our hospital for vomiting, dysarthria, and conscious disturbance. At 23, he underwent ligation of the left internal carotid artery (ICA) with superficial temporal artery to middle cerebral artery anastomosis because of acute infarct of the left hemisphere caused by arterial dissection of the left ICA. During the current admission, computed tomography (CT) revealed subarachnoid hemorrhage, and digital subtraction angiography (DSA) demonstrated dissecting aneurysms of the left intracranial vertebral artery (VA) and right extracranial VA. We diagnosed him with a ruptured dissecting aneurysm of the left intracranial VA and performed endovascular parent artery occlusion on the left VA. For the right unruptured VA aneurysm, we performed coil embolization simultaneously. At 2 weeks after the endovascular treatment, follow-up DSA revealed that multiple dissecting aneurysms developed on the origin of the left VA and left and right internal thoracic arteries. Those aneurysms were treated with coil embolization. Other remaining aneurysms on the left thyrocervical trunk, right transverse cervical artery, and both common iliac arteries were treated by conservative therapy. While continuing medical treatment for RA, the patient recovered and was discharged to a rehabilitation hospital.

CONCLUSION

Considering that RA-induced vasculitis can be a potential risk of vascular complications including multiple arterial dissections, physicians should carefully perform endovascular interventional procedures for patients with long-term RA.

摘要

目的

我们描述一例类风湿关节炎(RA)并发颅内和颅外多发性动脉夹层动脉瘤。

病例介绍

一名 29 岁男性,18 岁时被诊断为 RA,因左颈内动脉(ICA)夹层导致左半球急性梗死,行左侧颈内动脉结扎术+颞浅动脉-大脑中动脉吻合术。此次入院前,患者因呕吐、构音障碍和意识障碍就诊。入院时 CT 提示蛛网膜下腔出血,数字减影血管造影(DSA)显示左侧颅内椎动脉(VA)和右侧颅外 VA 夹层动脉瘤。诊断为左侧颅内 VA 破裂性夹层动脉瘤,行左侧 VA 血管内母动脉闭塞术。右侧未破裂 VA 动脉瘤同期行弹簧圈栓塞术。血管内治疗 2 周后,随访 DSA 显示左侧 VA 及左、右内乳动脉起始处多发性夹层动脉瘤。采用弹簧圈栓塞治疗。左颈总干、右横突颈及双侧髂总动脉残余动脉瘤采用保守治疗。在继续 RA 治疗的同时,患者恢复并出院至康复医院。

结论

考虑到 RA 引起的脉管炎可能是包括多发性动脉夹层在内的血管并发症的潜在危险因素,对于长期 RA 患者,医生应慎重进行血管内介入治疗。

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