A Very Rare Case of Coronary Artery Bypass Grafting in a Progeria Child.

Autor: Cerejo RPS; Cardiothoracic Surgery Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal., Rodrigues RAN; Cardiothoracic Surgery Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal., Martins JD; Pediatric Cardiology Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal., Torres CGEC; Thoracic Surgery Department, Hospital Pulido Valente-Centro Hospitalar Lisboa Norte, Lisbon, Portugal., Sousa LM; Cardiology Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal., Pinto FF; Pediatric Cardiology Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal., Fragata JIG; Cardiothoracic Surgery Department, Hospital de Santa Marta-Centro Hospitalar Lisboa Central, Lisbon, Portugal.
Jazyk: angličtina
Zdroj: World journal for pediatric & congenital heart surgery [World J Pediatr Congenit Heart Surg] 2020 Jul; Vol. 11 (4), pp. NP244-NP246. Date of Electronic Publication: 2019 Apr 23.
DOI: 10.1177/2150135118803596
Abstrakt: Hutchinson-Gilford progeria syndrome is a rare genetic disorder, characterized by progressive premature aging and early death in the first or second decade of life, usually secondary to cardiovascular events (myocardial infarction and stroke). We report a case of a 14-year-old boy with progeria syndrome and cardiac arrest due to myocardial infarction, who was submitted to an immediate coronary angiography which revealed left main stem and three-vessel coronary artery disease. A prompt double bypass coronary artery grafting surgery was performed, and, despite successful coronary reperfusion, the patient remained in coma and brain death was declared on fourth day after surgery.
Databáze: MEDLINE