Liesting Crista, Brugts Jasper Jan, Kofflard Marcellinus Johannes Maria, Dirkali Attila
Crista Liesting, Jasper Jan Brugts, Marcellinus Johannes Maria Kofflard, Attila Dirkali, Department of Cardiology, Albert Schweitzer Hospital, 3318 AT Dordrecht, The Netherlands.
World J Cardiol. 2012 Aug 26;4(8):264-6. doi: 10.4330/wjc.v4.i8.264.
Coronary artery anomalies are usually encountered as coincidental findings during coronary angiography or at autopsy. Life threatening symptoms, such as arrhythmias, syncope, myocardial infarction, or sudden death, can occur in up to 20% of patients. However, the majority of anomalies (80%) are benign and asymptomatic. A single coronary artery (SCA) is one of the most rarely seen coronary anomalies with an incidence of 0.05%. We report the case of a 55-year old male patient who presented with symptoms of chest pain associated with an acute myocardial infarction. Coronary angiography revealed an anomalous left main coronary artery (LMCA) originating from the right coronary ostium, and an occluded distal right coronary artery. The occluded distal right coronary artery was successfully treated by thrombosuction and stenting. In order to confirm the origin and course of the SCA, multi-slice computed tomography (MSCT) of the heart was performed after coronary angiography. MSCT showed that the anomalous LMCA originated from the right coronary artery ostium and then passed the interventricular septum, instead of being intra arterial, and under the right ventricular infundibulum. The anomalous LMCA was classified as R-II S subtype according to Lipton's classification.
冠状动脉异常通常是在冠状动脉造影或尸检时偶然发现的。高达20%的患者可能出现危及生命的症状,如心律失常、晕厥、心肌梗死或猝死。然而,大多数异常情况(80%)是良性且无症状的。单支冠状动脉(SCA)是最罕见的冠状动脉异常之一,发病率为0.05%。我们报告一例55岁男性患者,其出现与急性心肌梗死相关的胸痛症状。冠状动脉造影显示异常的左主干冠状动脉(LMCA)起源于右冠状动脉开口,右冠状动脉远端闭塞。通过血栓抽吸和支架置入成功治疗了闭塞的右冠状动脉远端。为了确认SCA的起源和走行,在冠状动脉造影后进行了心脏多层计算机断层扫描(MSCT)。MSCT显示异常的LMCA起源于右冠状动脉开口,然后穿过室间隔,而不是走行于动脉内,且位于右心室漏斗部下方。根据Lipton分类,异常的LMCA被归类为R-II S亚型。