Ugurlucan Murat, Sayin Omer Ali, Dayioglu Enver, Tireli Emin
Cardiovascular Surgery Clinic, Duzce Ataturk State Hospital, Duzce, Turkey.
J Card Surg. 2011 Jan;26(1):107-10. doi: 10.1111/j.1540-8191.2010.01165.x. Epub 2010 Dec 16.
Patent ductus arteriosus is one of the most common congenital cardiac pathologies, besides patency of ductus may be somewhat vital for various congenital cardiac defects, otherwise death is inevitable. Anatomically, ductus is single and located between the descending aorta and the pulmonary artery. The review of the literature reveals presence of more than one ductus arteriosi in sporadic cases, most commonly associated with aortic arch anomalies. In this report, we present a nine-month-old baby with the diagnosis of ventricular septal defect (VSD), pulmonary atresia (PA), nonconfluent pulmonary arteries, and bilateral patent ductus arteriosi. He underwent a successful pulmonary reconstruction and central-shunt operation with modified aortopulmonary window technique without cardiopulmonary bypass. This is a very rare case with double ductus arteriosi associated with VSD, PA, and nonconfluent pulmonary arteries.
动脉导管未闭是最常见的先天性心脏病变之一,此外,动脉导管的通畅对于各种先天性心脏缺陷可能至关重要,否则死亡不可避免。从解剖学上讲,动脉导管是单一的,位于降主动脉和肺动脉之间。文献回顾显示,在散发病例中存在不止一条动脉导管,最常见于与主动脉弓异常相关的情况。在本报告中,我们介绍了一名9个月大的婴儿,诊断为室间隔缺损(VSD)、肺动脉闭锁(PA)、肺不融合以及双侧动脉导管未闭。他接受了成功的肺重建和中心分流手术,采用改良的主肺动脉窗技术,无需体外循环。这是一例非常罕见的伴有双动脉导管未闭且与室间隔缺损、肺动脉闭锁和肺不融合相关的病例。