Ece Ibrahim, Uner Abdurrahman, Cuce Ferhat, Balli Sevket
Department of Pediatric Cardiology, Faculty of Medicine, Yuzuncu Yil University, Van, Turkey,
Cardiovasc Interv Ther. 2014 Oct;29(4):359-62. doi: 10.1007/s12928-013-0240-6. Epub 2014 Jan 4.
A right pulmonary artery-to-left atrial fistula is a very rare cyanotic congenital heart defect and is characterized by cyanosis and normal auscultation of the heart. Interventional closure of the fistula using occluder devices and coils has been rarely reported. We report the successful closure of a RPA-to-left atrial fistula using an Amplatzer muscular ventricular septal defect occluder in a child with cyanosis. The two-dimensional echocardiogram with bubble contrast study demonstrated the communication between right pulmonary artery and left atrium. Computerized tomography confirmed the diagnosis and delineated the anatomy.
右肺动脉至左心房瘘是一种非常罕见的青紫型先天性心脏缺陷,其特征为青紫且心脏听诊正常。使用封堵器和弹簧圈对该瘘进行介入封堵的报道很少。我们报告了1例使用Amplatzer肌部室间隔缺损封堵器成功封堵右肺动脉至左心房瘘的青紫患儿。二维超声心动图造影检查显示了右肺动脉与左心房之间的交通。计算机断层扫描证实了诊断并明确了解剖结构。