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首页> 外文期刊>Journal of Medical Cases >The Simultaneity of Coronary Artery Ectasia and Intracranial Arterial Dolichoectasia: A Case Report and Literature Review
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The Simultaneity of Coronary Artery Ectasia and Intracranial Arterial Dolichoectasia: A Case Report and Literature Review

机译:冠状动脉畸位和颅内动脉培养基型分子的同时性:案例报告和文献综述

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In the present study, we report a case of multiple coronary artery ectasias (CAE) and multiple intracranial arterial dolichoectasias (IADEs). A 60-year-old female presented to the emergency department twice with chest pain and mild elevation of troponin and T-wave changes. Peripheral coronary angiography showed severe ectasia and stenosis of certain segments of the left main coronary artery (LMCA), left anterior descending (LAD), first obtuse marginal (OM1), distal left circumflex (LCX), and bilateral subclavian arteries. The patient was treated medically. Two weeks later, she presented with dizziness. Head computerized tomography (CT) angiography showed severe IADE involving the vertebrobasilar system, intracranial internal carotid arteries, and bilateral middle cerebral arteries. No neurovascular intervention was performed due to the complexity of the findings. CAE is an abnormal dilatation of a coronary artery segment of at least 1.5 times the size of a normal coronary artery. The slow flow phenomenon may lead to ischemia and thrombosis, which can result in acute coronary syndrome. IADE comprises a dilatation and elongation of the arteries that affects both the anterior and posterior cerebral circulation, often causing neurological complications such as ischemic stroke, intracranial hemorrhage, or compression of surrounding neural structures. We report this case due to the rarity of coexisting IADE and CAE. A rarefaction of elastic tissue of the media with degeneration of the internal elastic lamina, in addition to matrix metalloproteinase dysfunction, is a common pathological mechanism for this condition. The management of CAE and IADE is mostly conservative, essentially treating the risk factors and administering antiplatelet and anticoagulant agents. In some patients, angioplasty vs. surgical treatment may be applied.
机译:在本研究中,我们报告了多个冠状动脉异位(CAE)和多个颅内动脉培养基酶(IADES)的情况。一位60岁的女性向急诊肿部呈现两次,胸痛和肌钙蛋白和T波的温和升高。外周冠状动脉造影显示左主冠状动脉(LMCA)的某些区段的严重异位和狭窄,左前期下降(LAD),首先钝边(OM1),远端左环(LCX)和双侧锁骨伏妇动脉。患者医学治疗。两周后,她带着头晕。头部计算机断层扫描(CT)血管造影显示严重的IADE涉及椎体系统,颅内内颈动脉和双侧中脑动脉。由于调查结果的复杂性,没有进行神经血管干预。 CAE是冠状动脉区段的异常扩张,其常规冠状动脉尺寸的至少1.5倍。缓慢的流动现象可能导致缺血和血栓形成,这可能导致急性冠状动脉综合征。 IADE包含影响前脑循环的动脉的扩张和伸长,通常导致神经系统并发症如缺血性卒中,颅内出血或周围神经结构的压缩。由于共存IADE和CAE的罕见,我们报告此案例。除了基质金属蛋白酶功能障碍之外,内部弹性薄层的变性具有变性的介质的弹性组织的稀疏性是这种条件的常见病理机制。 CAE和IADE的管理大多是保守的,基本上治疗危险因素和抗血小板和抗凝血剂。在一些患者中,可以应用血管成形术与手术治疗。

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