Ece Ibrahim, Uner Abdurrahman, Cuce Ferhat, Sahin Musa
Department of Pediatric Cardiology, Faculty of Medicine, Yuzuncu Yil University, Van, Turkey,
Cardiovasc Interv Ther. 2015 Apr;30(2):151-4. doi: 10.1007/s12928-014-0264-6. Epub 2014 Apr 17.
Congenital fistula between the aorta and right atrium is a rare congenital anomaly of the heart. We report a new case of this unusual communication, which was successfully closed by transcatheter embolisation using an Amplatzer duct occluder II. A 7-year-old asymptomatic girl was referred to our institute for evaluation of a murmur. Echocardiography revealed intact septae and the right coronary sinus was dilated with a fistulous tract arising from the sinus and opening into the right atrium with continuous flow into the right atrium. Computerized tomography confirmed the diagnosis and delineated the anatomy. Cardiac catheterization performed confirmed the presence of a markedly tortuous and dilated aorto-right atrial fistula. Coronary angiography demonstrated normal coronary arteries arising from the respective sinuses. The fistula was closed antegradely using an Amplatzer duct occluder II (AGA Medical Corporation, Plymouth, MN, USA). The continuous murmur had disappeared after the procedure and an echocardiogram revealed no continuous flow across the fistulous tract. The patient remained well at follow-up 3 months later.
先天性主动脉与右心房瘘是一种罕见的先天性心脏异常。我们报告了一例这种不寻常交通的新病例,使用Amplatzer II型动脉导管封堵器经导管栓塞成功闭合。一名7岁无症状女孩因杂音评估转诊至我院。超声心动图显示房间隔完整,右冠状动脉窦扩张,有一瘘管从窦部发出并开口于右心房,持续有血流进入右心房。计算机断层扫描确诊并明确了解剖结构。心导管检查证实存在明显迂曲扩张的主动脉-右心房瘘。冠状动脉造影显示冠状动脉分别起源于各自的窦部且正常。使用Amplatzer II型动脉导管封堵器(美国明尼苏达州普利茅斯市AGA医疗公司)顺行封堵瘘管。术后连续性杂音消失,超声心动图显示瘘管处无持续血流。3个月后随访,患者情况良好。