| Literature DB >> 35072407 |
Lys Molina Hernandes Estephan1, Aline Simões Aranda1, Carlos Henrique De Marchi1, Ulisses Alexandre Croti1.
Abstract
CLINICAL DATA: Patient diagnosed with common arterial trunk, submitted to pulmonary artery banding in another center and lost to clinical follow-up. Referred to our center at four years old, extremely cyanotic. Chest radiography: Cardiomegaly; attenuated peripheral vascular markings. Electrocardiography: Right ventricular hypertrophy. Echocardiography: Common arterial trunk, but it was not possible to analyze all the structures. Computed tomography angiography: Van Praagh type A4 common arterial trunk. Extremely hypoplastic right and left pulmonary arteries. DIAGNOSIS: Association of aortic arch interruption type A is uncommon and should be considered. OPERATION: Debanding of pulmonary arteries allowing for possible future complete repair.Entities:
Keywords: Aortic Coarctation; Cyanosis; Heart Defects, Congenital; Infant, Newborn; Truncus Arteriosus
Mesh:
Year: 2022 PMID: 35072407 PMCID: PMC8973140 DOI: 10.21470/1678-9741-2021-0008
Source DB: PubMed Journal: Braz J Cardiovasc Surg ISSN: 0102-7638