PDF herunterladen
J Pediatr Intensive Care 2021; 10(01): 079-082
DOI: 10.1055/s-0040-1709997
Case Report

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

Nak Hyun Choi
1   Division of Pediatric Cardiology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
,
Jenna Piccininni
1   Division of Pediatric Cardiology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
,
Michael Pollaro
2   Division of Neonatology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
,
Sabrina Law
1   Division of Pediatric Cardiology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
,
Sandhya Brachio
2   Division of Neonatology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
,
Allison Levey
1   Division of Pediatric Cardiology, Morgan Stanley Children's Hospital of NewYork-Presbyterian, Columbia University Medical Center, New York, United States
› Institutsangaben
› Weitere Informationen
Auch verfügbar auf
    Lizenzen und Reprints

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.

Keywords

coronary ostial atresia - coronary - myocardial ischemia


Publikationsverlauf

Eingereicht: 29. Januar 2020

Angenommen: 30. März 2020

Artikel online veröffentlicht:
29. April 2020

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 

  • References

  • 1 Polito A, Barrett CS, Wypij D. et al. Neurologic complications in neonates supported with extracorporeal membrane oxygenation. An analysis of ELSO registry data. Intensive Care Med 2013; 39 (09) 1594-1601
    CrossrefPubMedSuche in Google Scholar
  • 2 Morales DL. S, Rossano JW, VanderPluym C. et al; Pedimacs Investigators. Third annual pediatric interagency registry for mechanical circulatory support (Pedimacs) report: preimplant characteristics and outcomes. Ann Thorac Surg 2019; 107 (04) 993-1004
    CrossrefPubMedSuche in Google Scholar
  • 3 Olabiyi O, Kearney D, Krishnamurthy R, Morales D, Cabrera AG. First description of coronary artery ostial atresia with fistulous origin from a normal right ventricle. Pediatr Cardiol 2013; 34 (08) 1877-1881
    CrossrefPubMedSuche in Google Scholar
  • 4 Wein CE, Weinberg PM, Guleserian KJ. Congenital absence of coronary ostia in a single/common coronary system. Cardiol Young 2019; 29 (07) 993-995
    CrossrefPubMedSuche in Google Scholar
  • 5 Giglia TM, Mandell VS, Connor AR, Mayer Jr JE, Lock JE. Diagnosis and management of right ventricle-dependent coronary circulation in pulmonary atresia with intact ventricular septum. Circulation 1992; 86 (05) 1516-1528
    CrossrefPubMedSuche in Google Scholar