Abstract Number ‐ 138: Complex symptomatic dissecting pseudoaneurysm with inflow zone stenosis required angioplasty before flow‐diversion‐a technical report.

IF 2.1 Q3 CLINICAL NEUROLOGY
Y. Lodi, J. Campos
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引用次数: 0

Abstract

16.4 percent of patients diagnosed with fibromuscular dysplasia (FMD) are found to have internal carotid artery (ICA) dissection [1] which may lead to life threatening ICA dissecting pseudoaneurysm (ICADPA). Endovascular repair of ICADPA may be urgent when ICADPA is symptomatic, potential for rupture with no good alternatives. Tortuous anatomy with FMD and ICADS can represent a significant endovascular challenge, especially if there is an aneurysmal inflow‐zone stenosis.Objective: We present a unique case of right ICADPA with an inflow‐zone parent artery stenosis underwent angioplasty and repair with surpass evolve flow diverter (SEFD). Case report and chart review. 49‐year‐old man history of hypertension, hyperlipidemia, and left ICADPA status post stenting/stent‐assisted coiling in 2017, who presented with right‐sided pulsatile tinnitus after a facial injury. Cerebral angiography revealed a tortuous right ICA with FMD, and presence of a right ICADPA at the skull base measuring 16×8 mm with inflow zone stenosis and a post‐stenotic dilatation. An emergency repair was performed with an informed consent under general anesthesia. In order for the SEFD to deploy properly, an angioplasty of inflow‐zone parent artery stenosis was performed with a 3×20mm Maverick balloon. Subsequently, a SEFD measuring 5×40 mm was deployed to cover the dissecting pseudoaneurysm, and a second SEFD measuring 5×20 mm was deployed covering the ICADS resulting in good apposition of SEFD and securement of ICADS.Use of a metal self‐deployable stent prior to flow diversion was not an option due to the presence of extreme tortuosity and acute angulations on the parent artery.patient was discharged home after 24 hours with 325 mg of aspirin and 75 mg of clopidogrel and good blood pressure control. 90‐days follow‐up, demonstrated good recovery with modified Rankin score of 0 with no symptoms. ICADPA with aneurysmal inflow zone parent artery stenosis and the presence of extream tortuosity and acute angulations, may require angioplasty prior to the flow diversion for successful repair. Further studies are required.
摘要编号-138:复杂症状的夹层假性动脉瘤伴流入区狭窄,需要在分流前进行血管成形术——一份技术报告。
16.4%被诊断为纤维肌发育不良(FMD)的患者被发现有颈内动脉(ICA)夹层[1],这可能导致危及生命的颈内动脉夹层假性动脉瘤(ICADPA)。当ICADPA有症状时,ICADPA的血管内修复可能是紧急的,有可能破裂,没有好的替代方案。FMD和ICADS的扭曲解剖可能是一个重大的血管内挑战,尤其是在动脉瘤流入区狭窄的情况下。目的:我们报告了一例独特的右ICADPA患者,其母动脉流入区狭窄,采用超进化分流器(SEFD)进行血管成形术和修复。病例报告和图表审查。2017年,49岁男性,有高血压、高脂血症史,支架植入/支架辅助螺旋术后左ICADPA状态,面部损伤后出现右侧搏动性耳鸣。脑血管造影术显示右侧ICA弯曲伴FMD,颅底存在右侧ICADPA,尺寸为16×8 mm,流入区狭窄,狭窄后扩张。在全身麻醉下,在知情同意的情况下进行了紧急修复。为了使SEFD正确展开,使用3×20mm Maverick球囊对流入区母动脉狭窄进行了血管成形术。随后采用5×40mm的SEFD覆盖夹层假性动脉瘤,第二个尺寸为5×20mm的SEFD覆盖ICADS,从而使SEFD良好附着并固定ICADS。由于母体动脉存在极度扭曲和锐角,因此在分流前不能选择使用金属自展开支架。患者在服用325 mg阿司匹林和75 mg氯吡格雷24小时后出院血压控制。90天的随访显示,恢复良好,改良Rankin评分为0,无症状。ICADPA伴动脉瘤流入区母动脉狭窄,存在束外弯曲和急性成角,可能需要在分流前进行血管成形术才能成功修复。还需要进一步研究。
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