| Literature DB >> 30546646 |
Seiichi Taniai1, Kazuya Takemoto1, Wataru Nagai1, Yusuke Inaba2, Hidehito Endo2, Mio Noma2, Hiroshi Kubota2, Kenichi Sudo2, Konomi Sakata1, Toru Satoh1, Hideaki Yoshino1.
Abstract
We experienced two adult cases of anomalous origin of the left coronary artery from the pulmonary artery, so-called Bland-White-Garland (BWG) syndrome, that presented with ventricular tachycardia (VT) and ventricular fibrillation during exertion in daily life. They presented to our hospital with syncope due to VT, and recovered following application of an automated external defibrillator with cardiopulmonary resuscitation. We diagnosed BWG syndrome by multi-detector computed tomography angiography and coronary angiography. We analyzed the mechanisms of lethal arrhythmias in relation to myocardial ischemia on exertion. Coronary flow modification and implantable cardioverter defibrillator implantation were performed in order to prevent future lethal arrhythmia due to myocardial ischemia. It is important to be aware of congenital heart disease in ordinary cases. <Learning objective: We experienced two rare cases of patients who were admitted with ventricular tachycardia and ventricular fibrillation who had adult type Bland-White-Garland syndrome during exertion in daily life. It is important to be aware of congenital heart disease in ordinary cases.>.Entities:
Keywords: Anomalous origin of left coronary artery from pulmonary artery; Bland–White–Garland syndrome; Congenital; Ventricular tachycardia
Year: 2016 PMID: 30546646 PMCID: PMC6283018 DOI: 10.1016/j.jccase.2016.03.006
Source DB: PubMed Journal: J Cardiol Cases ISSN: 1878-5409