Erez Eldad, Tam Vincent K H, Doublin Nancy A, Stakes Jeanie
Cook Children's Medical Center, University of North Texas, Fort Worth, Texas 76104, USA.
Ann Thorac Surg. 2006 Sep;82(3):973-7. doi: 10.1016/j.athoracsur.2006.04.089.
Anomalous origin of a coronary artery with subsequent coursing between the great vessels is a rare congenital heart defect that may cause myocardial ischemia and sudden death. Because of the fatality rate of this anomaly, many are diagnosed at the postmortem examination, and reports of surgical correction are few. We present our experience with the diagnosis and surgical treatment of this rare coronary anomaly.
Between June 2003 and August 2005, 9 patients (8 males) were diagnosed with anomalous origin of a coronary artery coursing between the great vessels. The mean age was 12 +/- 5.8 years (range, 4 months to 23 years). Three patients had an intramural origin of the coronary artery. One infant had a single coronary artery and was diagnosed during follow-up of other heart defects. The 8 older patients all presented with exertional syncope or chest pain and echocardiography was used for the initial diagnosis. Six patients had coronary artery reimplantation in the correct aortic sinus, 2 patients had unroofing of the intramural coronary segment, and 1 patient had pericardial patch enlargement of his right coronary artery before reimplantation. One patient, the infant, awaits repair at an older age.
No postoperative deaths occurred. The mean hospital stay was 5.5 +/- 1.2 days (range, 4 to 8 days). Three patients had transient ST segment changes during the first 24 hours postoperatively. Follow-up was 4 months to 2.5 years. All patients underwent an exercise myocardial perfusion scan 3 months postoperatively without evidence of myocardial ischemia, and all patients remain clinically well.
Echocardiography imaging of young patients with exertional syncope or chest pain is reliable for the diagnosis of this coronary anomaly. It is surgically correctable; however, individual coronary anatomy may cause the surgical approach to vary. The postoperative outcome is excellent.
冠状动脉异常起源并走行于大血管之间是一种罕见的先天性心脏缺陷,可导致心肌缺血和猝死。由于这种异常的死亡率较高,许多病例是在尸检时才被诊断出来,手术矫正的报告较少。我们介绍我们对这种罕见冠状动脉异常的诊断和手术治疗经验。
2003年6月至2005年8月期间,9例患者(8例男性)被诊断为冠状动脉异常起源并走行于大血管之间。平均年龄为12±5.8岁(范围为4个月至23岁)。3例患者冠状动脉为壁内起源。1例婴儿为单一冠状动脉,在对其他心脏缺陷进行随访时被诊断出来。8例年龄较大的患者均表现为劳力性晕厥或胸痛,初始诊断采用超声心动图。6例患者在正确的主动脉窦进行了冠状动脉再植入,2例患者对壁内冠状动脉段进行了开窗,1例患者在再植入前用心包补片扩大了右冠状动脉。1例婴儿患者等待年龄稍大时进行修复。
术后无死亡病例。平均住院时间为5.5±1.2天(范围为4至8天)。3例患者术后24小时内出现短暂ST段改变。随访时间为4个月至2.5年。所有患者术后3个月均接受了运动心肌灌注扫描,未发现心肌缺血证据,所有患者临床状况良好。
对于有劳力性晕厥或胸痛的年轻患者,超声心动图成像对这种冠状动脉异常的诊断是可靠的。它可以通过手术矫正;然而,个体冠状动脉解剖结构可能导致手术方法有所不同。术后结果良好。