Di Eusanio G, Mazzola A, Gregorini R, Di Manici G, Esposito G P, Procaccini B, Paparoni S, De Curtis G, Di Luzio V
Dipartimento di Alta Specialità Medico-Chirurgica delle Malattie Cardiovascolari, Ospedale G. Mazzini, Villa Mosca, Teramo, Italy.
J Cardiovasc Surg (Torino). 1989 Jul-Aug;30(4):709-12.
Anomalous origin of one pulmonary artery from the ascending aorta without associated intracardiac defects is a rare congenital malformation. About 60 anatomic and surgical descriptions have been reported in the literature. Up to 1974, 22 of the 50 reported cases underwent surgical correction with a 40% mortality rate. The natural history without surgery is poor with a very high mortality during the first year of life. Successful anatomic correction of anomalous origin of right pulmonary artery from the ascending aorta in a 6 months old female is reported.
一根肺动脉从升主动脉异常起源且无相关心内缺损是一种罕见的先天性畸形。文献中已报道了约60例解剖和手术描述。截至1974年,在50例报道的病例中,有22例接受了手术矫正,死亡率为40%。未经手术的自然病程较差,在生命的第一年死亡率非常高。本文报道了一名6个月大女性升主动脉起源的右肺动脉异常起源的成功解剖矫正病例。