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首页> 外文期刊>European Heart Journal - Case Reports >Case report: spontaneous coronary artery dissection and suspicion of takotsubo cardiomyopathy in a patient presenting with T-wave inversions, severe QTc prolongation, elevated cardiac biomarkers, and apical akinesia
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Case report: spontaneous coronary artery dissection and suspicion of takotsubo cardiomyopathy in a patient presenting with T-wave inversions, severe QTc prolongation, elevated cardiac biomarkers, and apical akinesia

机译:案例报告:自发性冠状动脉解剖和涉及患者T波逆转,严重的QTC延长,心肌生物标志物和顶端疾病的患者患者患者

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Background In patients suspected of acute coronary syndrome, but where the coronary angiography (CAG) has shown unobstructed coronary arteries differential diagnoses include spontaneous coronary artery dissection and takotsubo cardiomyopathy. This case report presents a patient with spontaneous coronary artery dissection but diagnostic signs suspicious of takotsubo cardiomyopathy. Which leads to a consideration of the co-existence of the diseases. Case summary A 57-year-old woman was acutely admitted to the emergency ward with sudden development of chest discomfort, palpitations, and dyspnoea. At hospitalization, the electrocardiography showed T-wave inversions in I, aVL, and V2, and Troponin I was elevated. Initial echocardiography revealed apical akinesia consistent with takotsubo cardiomyopathy. Initially, a diagnosis of acute coronary syndrome or takotsubo cardiomyopathy was suspected. The patient was further diagnostically assessed with CAG including optical coherence tomography which showed spontaneous coronary artery dissection in the left anterior descending artery. At follow-up 3 months later, CAG showed a fully healed coronary artery, and repeated echocardiography showed normalization of the left ventricular function. Discussion In this case report, initially, acute coronary syndrome was suspected due to electrocardiography with T-wave inversions and elevated cardiac biomarkers. Takotsubo cardiomyopathy was suspected when echocardiography showed apical ballooning, but CAG with optical coherence tomography revealed a spontaneous coronary artery dissection. Interestingly no severe obstructions of coronary arteries were seen, and follow-up echocardiography showed fully regained myocardial function. This leads to the debate as to whether this might be a case of co-existing spontaneous coronary artery dissection and takotsubo cardiomyopathy.
机译:涉嫌急性冠状动脉综合征的患者的背景,但在冠状动脉血管造影(CAG)所示的情况下,冠心动脉鉴别诊断包括自发性冠状动脉解剖和Takotubo心肌病。本病例报告呈现出自发性冠状动脉解剖的患者,但诊断迹象可疑takotsubo心肌病。这导致审议疾病的共存。案例摘要一名57岁的女子急于进入急诊病房,突然发展胸部不适,心悸和呼吸困难。在住院期间,心电图显示I,AVL和V2中的T波逆转,肌钙蛋白I升高。初始超声心动图显示出与Takotsubo心肌病的顶端疾病症。最初,怀疑急性冠状动脉综合征或Takotubo心肌病的诊断。患者进一步用CAG进行诊断地评估,包括光学相干断层摄影,其在左前期下降动脉中显示出自发性冠状动脉夹层。在3个月后,CAG显示出完全愈合的冠状动脉,反复超声心动图显示左心室功能的标准化。在本例报告中讨论,最初,由于具有T波逆转和升高的心脏生物标志物的心电图,怀疑急性冠状动脉综合征。当超声心动图显示出顶线膨胀时,怀疑Takotubo心肌病,但具有光学相干断层扫描的CAG显示出自发性冠状动脉夹层。有趣地没有看到冠状动脉的严重障碍,随访超声心动图显示出完全恢复的心肌功能。这导致辩论,以及这是否可能是共同存在的自发性冠状动脉解剖和Takotubo心肌病的情况。

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