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首页> 外文期刊>Case Reports in Cardiology >Loeys-Dietz Syndrome Complicated by Right Coronary Artery Pseudoaneurysm
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Loeys-Dietz Syndrome Complicated by Right Coronary Artery Pseudoaneurysm

机译：Loeys-Dietz综合征合并右冠状动脉假性动脉瘤

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Loeys-Dietz syndrome is a rare autosomal dominant connective tissue disorder notable for rapidly progressive vascular aneurysmal disease and craniofacial defects. Patients are at an increased risk for aneurysm rupture and dissection at younger ages compared to other aneurysmal syndromes. Early surgical intervention is important for prevention of ruptures and/or dissection. The coronary arterial tree is mostly involved as a result of postoperative complications of an aortic root repair. This fact has been sparsely reported. We report a unique case of LDS2 presenting with chest pain that was later diagnosed as a pseudoaneurysm as a result of a right coronary artery graft dehiscence.
机译：Loeys-Dietz综合征是一种罕见的常染色体显性遗传结缔组织疾病，主要表现为快速进行性血管动脉瘤疾病和颅面缺陷。与其他动脉瘤综合征相比，患者在年轻时发生动脉瘤破裂和解剖的风险增加。早期手术干预对于预防破裂和/或解剖很重要。冠状动脉树主要是由于主动脉根部修复术后并发症所致。这个事实很少被报道。我们报告了LDS2出现胸痛的独特案例，后来被诊断为右冠状动脉移植物裂开的假性动脉瘤。

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