成人右肺动脉异常起源于升主动脉外科治疗2例报道  

Surgical treatment of the anomalous origin of the right pulmonary artery from ascending aorta in adults:a report of 2 cases

作　　者：杨兆华 杨晔 张红强 孙晓宁 刘欢 郭克芳 王春生 YANG Zhao-hua;YANG Ye;ZHANG Hong-qiang;SUN Xiao-ning;LIU Huan;GUO Ke-fang;WANG Chun-sheng(Department of Cardiac Surgery,Zhongshan Hospital,Fudan University,Shanghai 200032,China;Department of Anesthesiology,Zhongshan Hospital,Fudan University,Shanghai 200032,China)

机构地区：[1]复旦大学附属中山医院心外科,上海200032 [2]复旦大学附属中山医院麻醉科,上海200032

出　　处：《复旦学报（医学版）》2022年第6期1013-1016,共4页Fudan University Journal of Medical Sciences

摘　　要：肺动脉异常起源于升主动脉(anomalous origin of pulmonary artery from ascending aorta,AOPA)是一种罕见的先天性心脏病,通常合并动脉导管未闭。AOPA患者多在出生后不久即出现症状,如不及时治疗,很少能活到成年。本文报道2例成人右肺动脉起源于升主动脉的病例,通过正确的诊断和适当的手术治疗,获得良好的早中期疗效。Anomalous origin of pulmonary artery from ascending aorta(AOPA)is a rare congenital heart disease and the most common coexisting lesion is patent ductus arteriosus.Most patients present with this anomalous symptom during infancy and do not survive to adulthood without treatment.This paper reports two cases of adult right pulmonary artery originating from ascending aorta.Through correct diagnosis and appropriate surgical treatment,good early-and medium-term result was obtained.

关 键 词：先天性心脏病 肺动脉异常起源于升主动脉(AOPA) 肺动脉高压 

分 类 号：R654.2[医药卫生—外科学]