Clinical data: Infant, 11-month-old, male, diagnosis of Tetralogy of Fallot with
retrotracheoesophageal course of the brachiocephalic vein. Usual findings of
Tetralogy of Fallot on physical examination. Technical description: Chest
radiography showed slightly reduced pulmonary vascular markings and no
cardiomegaly. Normal preoperative electrocardiogram with postoperative right
bundle branch block. Usual findings of Tetralogy of Fallot on echocardiogram.
Postoperative computed tomography angiography confirmed left brachiocephalic
vein with anomalous retrotracheoesophageal course, configuring a U-shaped
garland vein, in addition to postoperative findings of total correction of
Tetralogy of Fallot. Operation: Complete surgical repair was performed with
pulmonary valve commissurotomy and placement of bovine pericardial patch to
solve right ventricular outflow tract obstruction, pulmonary trunk enlargement,
and ventricular septal defect closure. Comments: Systemic venous drainage may
show variations in patients with Tetralogy of Fallot. These abnormalities are
usually of little clinical relevance, as they are asymptomatic. We presented a
rare case of retrotracheoesophageal course of an anomalous left brachiocephalic
vein with intraoperative diagnosis, confirmed by imaging during postoperative
follow-up, without compromising clinical management or surgical approach.