A case of anomalous right coronary artery from the pulmonary trunk, aortopulmonary window, and interrupted aortic arch type a in a term neonate.

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Annals of Pediatric Cardiology Pub Date : 2025-01-01 Epub Date: 2025-07-14 DOI:10.4103/apc.apc_171_24
Ahlam Salim Atiq, Madan Mohan Maddali, Salim Nasser Al-Maskari, Faiza Abdullah Al Kindi, Sunny Zacharias
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引用次数: 0

Abstract

We report a case of a term neonate presenting with anomalous origin of the right coronary artery from the pulmonary trunk, an aortopulmonary window, interrupted aortic arch type A, and an atrial septal defect within the oval fossa. The infant, admitted in cardiogenic shock, was stabilized with fluid resuscitation, intubation, and inotropic support. Comprehensive imaging revealed the complex cardiac anomalies. Surgical intervention successfully addressed all the lesions. The patient showed excellent postoperative recovery, with no complications at 6 months. Our experience underscores the critical need for detailed preoperative assessment in managing complex congenital heart defects.

1例足月新生儿右冠状动脉异常,肺动脉窗,A型主动脉弓中断。
我们报告一例足月新生儿表现为右冠状动脉异常起源于肺动脉干,主动脉肺动脉窗,a型主动脉弓中断,以及卵圆窝内的房间隔缺损。该婴儿因心源性休克入院,经液体复苏、插管和肌力支持稳定。综合影像学显示复杂的心脏异常。手术治疗成功地解决了所有病变。患者术后恢复良好,6个月无并发症发生。我们的经验强调了在处理复杂的先天性心脏缺陷时进行详细的术前评估的重要性。
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来源期刊
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.40
自引率
14.30%
发文量
51
审稿时长
23 weeks
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