一例罕见的成人主肺动脉窗合并右肺动脉起源于主动脉异常并导致艾森曼格综合征
A Rare Case of Adult Aortopulmonary Window Combined with Anomalous Origin of the Right Pulmonary Artery from the Aorta Leading to Eisenmenger Syndrome.
作者信息
Cui Mingyue, Xia Binfeng, Wang Heru, Liu Haihui, Yin Xia
机构信息
Center for Cardiovascular Medicine, The First Hospital of Jilin University, Changchun, China.
Department of Cardiac Ultrasound, The First Hospital of Jilin University, Changchun, China.
出版信息
J Int Med Res. 2021 Jan;49(1):300060520984656. doi: 10.1177/0300060520984656.
Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery.
主肺动脉窗是一种罕见的先天性心脏病，可增加肺血管阻力，加重左向右分流，并导致心力衰竭和呼吸道感染。大多数患者在儿童期死亡。我们报告一例53岁男性患者，患有大型主肺动脉窗并合并右肺动脉起源于主动脉异常，患有艾森曼格综合征且未接受手术治疗。
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