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Recurrent myocardial infarction due to coronary artery aneurysm in Beh?et’s syndrome: a case report

机译:贝赫特氏综合征因冠状动脉瘤而复发的心肌梗死:一例报告

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Background Beh?et’s syndrome (BS) is a multisystemic vasculitis of unknown aetiology. Coronary involvement is extremely uncommon in BS, with a reported prevalence of 0.5%. The mortality of cardiovascular manifestation in BS is 20%, while there are still considerable challenges in the management of these patients.Case summaryWe report the case of a 30-year-old young man with a 12-year history of BS complicated by left anterior descending coronary (LAD) aneurysms, stenosis, and recurrent myocardial infarction. Percutaneous coronary intervention treated the stenosis and aneurysms of the LAD, but the coronary angiography clearly revealed an acute stent thrombosis after 7?months. This unusual coronary complication of BS treated successfully is presented.DiscussionOur case demonstrated the feasibility of covered stent, immunosuppressive therapy, and escalated antithrombotic regimen in the treatment of BS patients with coronary artery aneurysm (CAA). We also demonstrated that drug-eluting stents may aggravate aneurysmal dilatation of the CAA under inefficient immunosuppressive therapy.
机译:背景行为综合征(BS)是病因不明的多系统性血管炎。冠状动脉受累在BS中极为罕见,据报道患病率为0.5%。 BS的心血管表现的死亡率为20%,但在这些患者的治疗方面仍然存在相当大的挑战。病例总结我们报道了一名30岁的年轻人,该患者具有BS的12年病史并伴有左前冠状动脉(LAD)下降,狭窄和复发性心肌梗塞。经皮冠状动脉介入治疗了LAD的狭窄和动脉瘤,但冠状动脉造影明确显示在7个月后出现急性支架血栓形成。介绍了成功治疗的这种罕见的BS冠状动脉并发症。讨论我们的病例证明了覆膜支架,免疫抑制疗法和逐步的抗血栓形成方案治疗BS冠状动脉瘤(CAA)患者的可行性。我们还证明了在无效的免疫抑制治疗下,药物洗脱支架可能会加剧CAA的动脉瘤扩张。

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