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本文引用的文献

1
Congenital absence of coronary ostia in a single/common coronary system.单支/共同冠状动脉系统中冠状动脉口先天性缺失
Cardiol Young. 2019 Jul;29(7):993-995. doi: 10.1017/S1047951119001100. Epub 2019 Jun 21.
2
Third Annual Pediatric Interagency Registry for Mechanical Circulatory Support (Pedimacs) Report: Preimplant Characteristics and Outcomes.第三届儿科机械循环支持机构间注册研究（Pedimacs）报告：植入前特征和结局。
Ann Thorac Surg. 2019 Apr;107(4):993-1004. doi: 10.1016/j.athoracsur.2019.01.038. Epub 2019 Feb 26.
3
Neurologic complications in neonates supported with extracorporeal membrane oxygenation. An analysis of ELSO registry data.体外膜肺氧合支持新生儿的神经并发症。ELSO 登记数据的分析。
Intensive Care Med. 2013 Sep;39(9):1594-601. doi: 10.1007/s00134-013-2985-x. Epub 2013 Jun 8.
4
First description of coronary artery ostial atresia with fistulous origin from a normal right ventricle.首例起源于正常右心室且伴有瘘管的冠状动脉开口处闭锁的描述。
Pediatr Cardiol. 2013;34(8):1877-81. doi: 10.1007/s00246-012-0427-0. Epub 2012 Aug 8.
5
Diagnosis and management of right ventricle-dependent coronary circulation in pulmonary atresia with intact ventricular septum.
Circulation. 1992 Nov;86(5):1516-28. doi: 10.1161/01.cir.86.5.1516.

一名足月新生儿产后早期死亡，其冠状动脉开口闭锁。

Atretic Coronary Artery Ostia in a Full-Term Infant with Early Postnatal Demise.

作者信息

Choi Nak Hyun, Piccininni Jenna, Pollaro Michael, Law Sabrina, Brachio Sandhya, Levey Allison

机构信息

Division of Pediatric Cardiology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States.

Division of Neonatology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States.

出版信息

J Pediatr Intensive Care. 2021 Mar;10(1):79-82. doi: 10.1055/s-0040-1709997. Epub 2020 Apr 29.

DOI:10.1055/s-0040-1709997
PMID:33585067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7870342/
Abstract

Congenital coronary artery anomalies are extremely rare causes of early cardiac failure. Several cardiac lesions are associated with coronary anomalies such as pulmonary atresia with intact ventricular septum. Isolated coronary ostial atresia is extremely rare and described in only a few published case reports. To our knowledge, there were two reports of bilateral coronary ostial atresia in which the entire coronary arterial system originated from the right ventricle without other intracardiac defects. We present a case of a full-term infant who presented with severely depressed biventricular function secondary to bilateral coronary ostial atresia.

摘要

先天性冠状动脉异常是早期心力衰竭极为罕见的病因。几种心脏病变与冠状动脉异常相关，如室间隔完整的肺动脉闭锁。孤立性冠状动脉开口处闭锁极为罕见，仅有少数已发表的病例报告对此进行了描述。据我们所知，有两份关于双侧冠状动脉开口处闭锁的报告，其中整个冠状动脉系统起源于右心室且无其他心内缺陷。我们报告一例足月婴儿，因双侧冠状动脉开口处闭锁继发严重的双心室功能不全。