血管内治疗血管型Ehlers-Danlos综合征患者,伴有双侧椎动脉V3和V4段夹层狭窄和动脉瘤

Y. Cherednychenko, A.Yu. Miroshnychenko, L. Dzyak, N. A. Zorin, S. Grygoruk, E. Gavva, A. N. Tolubaiev
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引用次数: 0

摘要

描述了一例4型埃勒斯-丹洛斯综合征患者的治疗病例,该患者患有椎动脉V3和V4段的双侧夹层狭窄和动脉瘤。另一个血管异常也被证实:异常的右锁骨下动脉(卢索里亚动脉)。颈部动态旋转的脑血管造影显示了弓猎人综合征,该综合征包括当头部向左旋转时右椎动脉的血流受到限制。对两条椎动脉进行了分期血管内重建。首先,将LVIS支架植入解剖病变水平的左椎动脉。然后,用可拆卸线圈栓塞左椎动脉瘤。使用顺应性球囊导管Scepter在支架段进行球囊血管成形术。在一系列血管造影照片上:动脉瘤被完全排除,动脉狭窄被消除。1个月后,在右侧椎动脉进行相同体积的第二阶段血管内治疗。尝试使用血管闭合装置进行止血时,两次手术均未成功。通过手动按压穿刺部位成功止血。负责III型前胶原合成的COL3A1基因突变在随后的患者基因分型中被4型(血管型)埃勒斯-丹洛斯综合征证实。病人的神经系统症状在很大程度上消退了。血管内方法可有效治疗血管型埃勒斯-丹洛斯综合征患者的椎动脉夹层病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endovascular treatment of the patient with vascular type of Ehlers–Danlos syndrome with bilateral dissection stenoses and aneurysms in V3- andV4- segments of vertebral arteries
A case of treatment of a patient with type 4 of Ehlers–Danlos syndrome and bilateral dissection stenoses and aneurysms in V3and V4-segments of vertebral arteries is described. Also another vascular anomaly was verified: the aberrant right subclavian artery (arteria lusoria). Сerebral angiography with dynamic rotation of the neck revealed a bow hunter's syndrom, which consists in the restriction of blood flow in the right vertebral artery when the head is turned to the left. Stage-by-stage endovascular reconstruction of both vertebral arteries was performed. Firstly, LVIS stent was implanted in the left vertebral artery on the level of the dissection lesion. Then, the aneurysm of the left vertebral artery was embolized by detachable coils. Balloon angioplasty was performed in the stented segment with the compliance balloon-catheter Scepter. On the series of angiograms: the aneurysm is totally excluded, the stenosis of the artery is eliminated. After 1 month, the second stage of endovascular treatment in the same volume in the right vertebral artery was performed. At attempts of a hemostasis with the vascular closure device Аngioseal were unsuccessful in both operations. Hemostasis was successfully performed by manual compression of the puncture site. A mutation in the gene COL3A1, responsible for the synthesis of procollagen III type, was confirmed by Ehlers–Danlos syndrome of type 4 (vascular type) at the subsequent genotyping of the patient. The patient's neurological symptoms regressed to a great extent. Endovascular methods can be effective in the treatment of vertebral arteries dissection lesions in patients with vascular type of Ehlers–Danlos syndrome.
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