Left Innominate Artery With Anomalous Origin From the Pulmonary Trunk: A Case Report of an Unnoticed Malformation

Juan D. Ayala Torres, Marcia Mejía Velasquez, Mónica Royero-Arias
Universidad de Antioquia. Clínica las Américas. Servicios de Salud San Vicente Fundación.
Columbia

Cureus
Cureus 2025; 17:
DOI: 10.7759/cureus.79661

Abstract
Thoracic vascular congenital anomalies are malformations with significant clinical implications. One of the rarest anomalies is the anomalous origin of the brachiocephalic trunk from the pulmonary trunk, often associated with serious complications such as pulmonary hypertension. Diagnosis is facilitated by advanced imaging techniques, including MRI and CT scans. We present a case of a premature newborn with congenital heart disease (hypoplastic right ventricle) who developed respiratory and septic complications. A CT angiography revealed a left innominate artery arising from the pulmonary trunk. Despite valvuloplasty and multidisciplinary management, the infant passed away at two and a half months due to multi-organ failure. Early diagnosis and interdisciplinary management, aided by advanced imaging techniques such as CT angiography, are crucial for improving outcomes in patients with complex congenital heart malformations.

Category
Class I. Pulmonary Hypertension Associated with Congenital Cardiovascular Disease
Diagnostic Testing for Pulmonary Vascular Disease. Non-invasive Testing

Age Focus: Pediatric Pulmonary Vascular Disease

Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication

Article Access
Free PDF File or Full Text Article Available Through PubMed or DOI: Yes

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