一名患有法洛四联症、合并双主动脉弓及冠状动脉动静脉瘘的青少年的肺动脉异常起源。
Anomalous origin of a pulmonary artery in a teenager with tetralogy of Fallot with associated double aortic arch and coronary arteriovenous fistula.
作者信息
Agrawal Vishal, Solanki Parth, Shah Ritesh, Parmar Divyakant, Mishra Amit
机构信息
Department of Cardiovascular and Thoracic Surgery,U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad),Civil Hospital Campus, Asarwa,Ahmedabad 380016,India.
Department of Cardiac Anaesthesia,U.N. Mehta Institute of Cardiology and Research Center (affiliated to B.J. Medical College, Ahmedabad),Civil Hospital Campus, Asarwa, Ahmedabad 380016,India.
出版信息
Cardiol Young. 2019 May;29(5):727-729. doi: 10.1017/S1047951119000933. Epub 2019 May 28.
We report the case of a 14-year-old female who had tetralogy of Fallot along with anomalous origin of the left pulmonary artery from the ascending aorta with co-dominant double aortic arch forming a complete vascular ring compressing the oesophagus along with a left main coronary artery to right ventricular outflow tract fistula. She underwent surgical correction without conduit placement.
我们报告了一例14岁女性病例，该患者患有法洛四联症，同时左肺动脉起自升主动脉且伴有共同优势型双主动脉弓，形成一个完整的血管环压迫食管，还存在左冠状动脉主干至右心室流出道瘘。她接受了无需置入管道的手术矫正。
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