Extremely late presentation of children with transposition the great arteries

Fakhri, Dicky; Busro, Pribadi Wiranda; Rahmat, Budi; Purba, Salomo; Roebiono, Poppy Surwianti; Ardiansyah, Ardiansyah

doi:10.1177/0218492320976291

Cited by 1 publication

(1 citation statement)

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“…Our index case had complete TGA Type 1, with intact interventricular septum (IVS) although it presented late due to high level of intracardiac mixing occurring thought the moderate sized ASD and a large PDA. Similar presentations have been earlier mentioned by many other authors [8][9][10][11].…”

Section: Discussionsupporting

confidence: 90%

Echocardiographic imaging of neonatal transposition of great arteries: Rare case report and review of literature

Akhil Mehrotra,

Faiz Illahi Siddiqui,

Ujala Shakya

et al. 2024

World J. Bio. Pharm. Health Sci.

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Transposition of the great arteries (TGA) is a congenital conotruncal abnormality characterized by discordant connections between the ventricles and great arteries, with the aorta originating from the right ventricle (RV), and the pulmonary artery (PA) originating from the left ventricle (LV). The two main types of TGA are complete transposition or dextro-transposition of the great arteries (D-TGA), commonly referred to as D-loop, and congenitally corrected transposition (CCTGA), commonly referred to as L-loop or L-TGA. In D-TGA, the connections between the ventricles and atria are concordant, whereas in CCTGA they are discordant, with the left atrium connected to the RV, and the right atrium connected to the LV. Imaging plays an important role in the evaluation of TGA, both before and after surgery, for helping define the anatomy, quantify hemodynamics, and evaluate complications. Transthoracic echocardiography is the first-line imaging modality for pre-surgical planning in children with TGA. MRI provides comprehensive morphologic and functional information, particularly in adults after surgery. CT is performed when MRI is contraindicated or expected to generate artifacts. We are reporting an extremely rare and unique case of 25-day old male neonate, suffering from TGA with a side to side alignment of great arteries, accompanied by a moderate sized restrictive atrial septal defect (ASD) and an ascending aortic aneurysm (AAA).

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Section: Discussionsupporting

confidence: 90%