Demir Mehmet
Department of Cardiology, Isparta State Hospital, Isparta, Turkey.
Turk Kardiyol Dern Ars. 2009 Oct;37(7):490-2.
Bicuspid aortic valve is one of the most common congenital heart valve disorders. We present the development of acute myocardial infarction (AMI) in an 18-year-old male patient with unrecognized bicuspid aortic valve and moderate aortic regurgitation. He presented with chest pain. The electrocardiogram showed ST-segment elevation in leads V2 to V6. Creatine kinase-MB level was elevated to 97 U/l and troponin I was very high (45,000 ng/ml). The diagnosis was made as anterior wall AMI. Following treatment with intravenous rt-PA, ST-segment elevation completely returned to normal. Transthoracic echocardiography showed a bicuspid aortic valve, moderate aortic regurgitation, and apical wall hypokinesia; left ventricular global systolic function was normal. The patient had no risk factors for coronary atherosclerosis, nor a history of substance addiction or a family history of coronary artery disease. Protein C, protein S and homocysteine levels were normal. He refused any further intervention. Two weeks after discharge, he presented again with chest pain. Electrocardiography, cardiac markers, and coronary arteriography were normal. He was discharged on appropriate medical treatment. The presented case is the first report of AMI in a patient with bicuspid aortic valve.
二叶式主动脉瓣是最常见的先天性心脏瓣膜疾病之一。我们报告了一名18岁男性患者,患有未被识别的二叶式主动脉瓣和中度主动脉瓣反流,发生了急性心肌梗死(AMI)。他因胸痛就诊。心电图显示V2至V6导联ST段抬高。肌酸激酶-MB水平升高至97 U/l,肌钙蛋白I非常高(45,000 ng/ml)。诊断为前壁AMI。静脉注射rt-PA治疗后,ST段抬高完全恢复正常。经胸超声心动图显示二叶式主动脉瓣、中度主动脉瓣反流和心尖壁运动减弱;左心室整体收缩功能正常。该患者没有冠状动脉粥样硬化的危险因素,也没有药物成瘾史或冠心病家族史。蛋白C、蛋白S和同型半胱氨酸水平正常。他拒绝了任何进一步的干预。出院两周后,他再次因胸痛就诊。心电图、心脏标志物和冠状动脉造影均正常。给予适当药物治疗后出院。本病例是二叶式主动脉瓣患者发生AMI的首例报告。