Zhang Xing, Su Zhongjian, Yang Yanfei, Ge Liping, Li Bin
Department of Cardiology, Kunming Children's Hospital, Kunming, China.
Front Pediatr. 2020 Sep 8;8:524. doi: 10.3389/fped.2020.00524. eCollection 2020.
Congenital descending aorta-right atrial tunnel is a rare congenital heart defect. Herein, a new case successfully treated by transcatheter closure using a new type of ventricular septal defect occluder from the aortic side was reported. An 11-month-old Chinese girl presenting with a cardiac murmur was suspected with partial anomalous pulmonary venous connection as assessed by echocardiography. Descending aorta-right atrial tunnel was confirmed by computed tomography angiography and cardiac catheterization. Subsequently, transcatheter closure was performed successfully using a new type of ventricular septal defect occluder from the aortic side. The cardiac murmur disappeared after the intervention, and echocardiography did not reveal any abnormal flow inside the right atrium. At 6 months, the patient had no murmur, and no residual shunt was found using the echocardiogram. Descending aorta-right atrial tunnel is a rare anomaly. Transcatheter closure was successful in our case. Long-term follow-up is needed to assess any progressive growth of the residual tunnel.
先天性降主动脉-右心房通道是一种罕见的先天性心脏缺陷。在此,报告了一例使用新型室间隔缺损封堵器经导管从主动脉侧成功封堵的新病例。一名11个月大的中国女童因心脏杂音就诊,经超声心动图评估怀疑为部分性肺静脉异位连接。计算机断层血管造影和心导管检查证实为降主动脉-右心房通道。随后,使用新型室间隔缺损封堵器经导管从主动脉侧成功进行了封堵。干预后心脏杂音消失,超声心动图未显示右心房内有任何异常血流。6个月时,患者无杂音,超声心动图未发现残余分流。降主动脉-右心房通道是一种罕见的异常情况。我们的病例经导管封堵成功。需要长期随访以评估残余通道是否有任何渐进性生长。