Donofrio M T, Ramaciotti C, Weinberg P M, Murphy J D
Division of Cardiology, Children's Hospital of Philadelphia, PA 19104, USA.
Pediatr Cardiol. 1995 May-Jun;16(3):147-9. doi: 10.1007/BF00801916.
We present a case of interruption of the aortic arch (IAA) in association with aortic atresia. A pulmonary artery to ascending aorta fistulous channel at the level of the sinuses of Valsalva of the pulmonary artery was present and supplied the ascending aorta and coronary arteries. The communication had a significant length, so embryologically it is not an aortopulmonary window. There have been only three reported cases in the literature of IAA with aortic atresia; in none was a pulmonary artery to ascending aorta fistulous tract present.
我们报告一例主动脉弓中断(IAA)合并主动脉闭锁的病例。在肺动脉瓣窦水平存在一条从肺动脉到升主动脉的瘘管通道,为升主动脉和冠状动脉供血。该交通支有相当长的长度,因此从胚胎学角度来看,它并非主肺动脉窗。文献中仅报道过三例IAA合并主动脉闭锁的病例;均未发现有从肺动脉到升主动脉的瘘管。