Case report discussion of management of pink tetralogy of Fallot in VACTERL association

Bayushi Eka Putra (Department of Cardiology and Vascular Medicine, Universitas Indonesia Medical School/National Cardiovascular Centre Harapan Kita, Jakarta)
Toto Wisnu Hendrarto (Subdivision of Perinatology, Department of Pediatric, Women and Children Hospital Harapan Kita, Jakarta)

Paediatrica Indonesiana
Vol 59 No 3 (2019): May 2019

Tetralogy of Fallot (TOF) and VACTERL are considered rare entities requiring medical attention with regards to diagnosis and management. When TOF is associated with VACTERL association, case management might differ from a simple case of TOF. Tetralogy of Fallot (TOF) is defined as a complex congenital cardiac abnormality characterized by ventricular septal defect, right outflow tract obstruction, right ventricular hypertrophy, and overriding aorta.1 The term was coined in 1888 by Fallot of Marseilles, even though the defect had been described in 1673 by Steno of Denmark. The entity was then studied extensively to deliver better care management through medical and surgical approaches.2