We report a 67-year-old woman who was diagnosed at adulthood a rare and complex congenital heart disease: a corrected transposition of the great vessels and situs inversus.
Patient presented with progressive worsening right heart failure (NYHA class 2).
A cardiac MDCT scan was scheduled to plan surgical tricuspid replacement.
According to the segmental analysis using axial slices, MDCT showed situs inversus and atrio-ventricular discordance ( Fig. 1 ), associated with ventriculo-arterial discordance ( Fig. 2 ). In addition, unique coronary artery was disclosed using 3D images ( Fig. 3 ).