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Huge Left Atrial Myxoma and Concomitant Silent Coronary Artery Disease in a Young Man

机译:一名年轻男子的巨大左心房粘液瘤和伴随的无声冠状动脉疾病

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摘要

Severe but silent coronary artery disease may rarely exist in young patients with a low-risk profile but with a family history of coronary artery disease. We describe the case of a 33-year-old Caucasian male with progressive shortness of breath caused by a huge left atrial myxoma who was diagnosed to have significant coronary artery disease in the preoperative assessment. After investigations, the patient underwent resection of the left atrial tumor and coronary artery bypass grafting (CABG) with a successful outcome. Even in the case of a young male, it may be prudent to investigate silent coronary artery disease in the presence of cardiovascular risk factors and family history of coronary artery disease. The learning objective of this case is to debate about the usefulness of a preoperative coronary study even in the young population with cardiac nonischemic pathologies (ie, valve pathology, cardiac tumors, etc.).
机译:低危型但有冠心病家族史的年轻患者可能很少存在严重但无声的冠状动脉疾病。我们描述了一名33岁的白人男性患者的病例,该患者由巨大的左心房粘液瘤引起的进行性呼吸急促,在术前评估中被诊断为患有严重的冠状动脉疾病。经过调查,该患者接受了左心房肿瘤切除术并冠状动脉搭桥术(CABG)取得了成功的结果。即使是年轻男性,在存在心血管危险因素和冠心病家族史的情况下,也应谨慎研究无症状冠心病。该病例的学习目标是就术前冠状动脉研究的有用性进行辩论,即使在患有心脏非缺血性病变(即瓣膜病变,心脏肿瘤等)的年轻人群中也是如此。

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