Key result
Cardiac CT successfully delineates complex anatomy in uncorrected Tetralogy of Fallot with right hemitruncus.
Why the study?
The association of tetralogy of Fallot with anomalous aortic origin of pulmonary artery (hemitruncus) is exceedingly rare, and survival into adulthood without surgical correction poses a management challenge.
Case Report (n=1)
No
Cardiac CT provides non-invasive, high-resolution anatomical delineation crucial for diagnosing and planning treatment in complex adult congenital heart diseases like TOF with Hemitruncus.
Rare adult TOF-hemitruncus survival via MAPCAs merits inclusion in hemoptysis differentials; leaves optimal management open.
Tetralogy of Fallot (TOF) is one of the most common congenital cardiac anomalies.The association of TOF with anomalous aortic origin of pulmonary artery (Hemitruncus) is, however, exceedingly rare.Survival into adulthood without surgical correction is itself unusual and typically depends on compensatory Major Aortopulmonary Collateral Arteries (MAPCAs).We present a case of a 30-year-old man who presented with recurrent hemoptysis and cough.Electrocardiogram (ECG)-gated cardiac computed tomography (CT) revealed the classical features of TOF, along with an atretic main pulmonary artery, right Hemitruncus, and reformation of the left pulmonary artery by multiple MAPCAs.This case illustrates the role of Cardiac CT for this exceptionally rare congenital heart anomaly in an adult survivor for anatomy delineation and treatment planning in this setting, which poses a management challenge.
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Choudhary et al. (2026) conducted a case report in Uncorrected Tetralogy of Fallot with Right Hemitruncus (n=1). Cardiac Computed Tomography was evaluated. Cardiac computed tomography successfully delineated the complex anatomy of uncorrected Tetralogy of Fallot with right hemitruncus and MAPCA-dependent left pulmonary circulation in an adult survivor.
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