Malekahmadi M, Shahmohammadi A
Pediatic Department, Hajar Hospital, Shahrekord University of Medical Sciences, Iran.
Pediatr Cardiol. 2005 Jul-Aug;26(4):328-30. doi: 10.1007/s00246-004-0656-y.
Coronary artery fistula (CAF) is a rare congenital anomaly that can be complicated by endocarditis, myocardial infarction, or coronary aneurysms. This article reviews the clinical characteristics and surgical outcome of 10 patients with CAF in Rajae Heart Center. From 1990 to 2000, 10 patients (age, 6 months to 15 years; mean age, 8.5 years) were diagnosed with CAF by echocardiography and cardiac catheterization. Six were female and 4 were male. All patients with isolated CAF (9) were asymptomatic. One patient with associated anomaly (mitral valve prolapse with severe mitral regurgitation) had dyspnea on exertion and palpitation. Five fistulas originated from the right coronary artery-three from the left and two from the left circumflex. Drainage was to the right ventricle (7), right atrium (2), and pulmonary artery (1). The ratio of pulmonary to systemic flow ranged between 1 and 1.6. All patients had surgical ligation. In the symptomatic patient, in addition to ligation, mitral valve replacement was performed. There was no operative or late death. Follow-up evaluation (range, 1-6 years; mean, 4.2 years) showed no evidence of recurrent or residual CAF. Surgical management of CAF is a safe and effective treatment resulting in 100% survival and clousure rate.
冠状动脉瘘(CAF)是一种罕见的先天性异常,可并发心内膜炎、心肌梗死或冠状动脉瘤。本文回顾了拉贾伊心脏中心10例CAF患者的临床特征和手术结果。1990年至2000年,10例患者(年龄6个月至15岁;平均年龄8.5岁)经超声心动图和心导管检查确诊为CAF。6例为女性,4例为男性。所有孤立性CAF患者(9例)均无症状。1例合并异常(二尖瓣脱垂伴严重二尖瓣反流)的患者有劳力性呼吸困难和心悸症状。5例瘘起源于右冠状动脉,3例起源于左冠状动脉,2例起源于左旋支。引流至右心室(7例)、右心房(2例)和肺动脉(1例)。肺循环与体循环血流量之比在1至1.6之间。所有患者均接受了手术结扎。有症状的患者除结扎外,还进行了二尖瓣置换术。无手术或晚期死亡病例。随访评估(范围1至6年;平均4.2年)显示无CAF复发或残留迹象。CAF的手术治疗是一种安全有效的治疗方法,生存率和闭合率均为100%。