一个微小的奇迹:在肺动脉手术后的左冠状动脉后,在一个小的新生儿中放置左侧冠状动脉支架
Bekir Yükcü1, Samet Paksoy1, Sezen Ugan Atik1
1Department of Pediatric Cardiology, University of Health Sciences, Istanbul Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey.
Cardiology in the young
|November 11, 2024
概括
来自肺动脉的异常左冠状动脉 (ALCAPA) 是一种罕见的先天性心脏缺陷. 透导管冠状动脉支架为手术后冠状动脉狭窄症的婴儿提供了一种拯救生命的解决方案.
科学领域:
- 心脏病学 心脏病学
- 儿童心脏病学 儿童心脏病学
- 遗传性心脏病是一种先天性心脏病.
背景情况:
- 来自肺动脉的异常左冠状动脉 (ALCAPA) 是一种罕见的先天性心脏缺陷,占所有先天性心脏缺陷 (CHD) 的0.5%.
- 植入鼻腔的左冠状动脉冠状动脉狭窄是ALCAPA手术修复后的一个已知的并发症.
- 在新生儿和婴儿中治疗术后冠状动脉狭窄症具有重大临床挑战.
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