Coronary artery patch augmentation for congenital left coronary ostial stenosis in Williams syndrome.
Coronary artery
Coronary artery ostial stenosis
Coronary artery patch augmentation
Williams syndrome
Journal
Multimedia manual of cardiothoracic surgery : MMCTS
ISSN: 1813-9175
Titre abrégé: Multimed Man Cardiothorac Surg
Pays: England
ID NLM: 101495626
Informations de publication
Date de publication:
20 Aug 2021
20 Aug 2021
Historique:
entrez:
12
11
2021
pubmed:
13
11
2021
medline:
26
11
2021
Statut:
epublish
Résumé
Left coronary ostial stenosis, which is associated with sudden death, occasionally occurs in individuals with Williams syndrome. However, surgical methods that provide reliable long-term revascularization remain unknown among infants and young children with coronary ostial stenosis. We describe the case of an 18-month-old boy with Williams syndrome who presented with cardiogenic shock due to left coronary ostial stenosis. We performed patch augmentation of the left coronary ostium using glutaraldehyde-treated autologous pericardium. At the last follow-up, the patient was well without any adverse events or myocardial ischemia.
Identifiants
pubmed: 34767699
doi: 10.1510/mmcts.2021.062
doi:
Types de publication
Case Reports
Video-Audio Media
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author 2021. Published by MMCTS on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.