Anomalous origin of Left Coronary Artery from Pulmonary Artery; Congenital Anomaly Presenting with Dyspnea. A rare Case Study
Abstract
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is rare congenital anomaly. Most of these patients die is infancy. Presentation in adulthood is very rare. Clinical manifestation in teenagers or young adult contains arrhythmia, myocardial perfusion likely causes significant chest pain and these symptoms of myocardial ischemia may be misinterpreted as routine infantile colic and sudden death.
Keywords
Kaynakça
- Nicholas T. Kouchoukos, Eugene H. Blackstone, Frank L. Hanley, and James K. Kirklin, Cardiac surgery: kilkilin Barratt — boyes. Fourth edition. 2013. p. 1650-62.
- Jonas RA. Comprehensive surgical management of congenital heart disease. 2014. p. 663-71.
- Parale GP, Pawar SS. Adult type anomalous left coronary artery from pulmonary artery, case report. 2006; 54:397-9.
- Brooks H. two case of abnormal coronary artery of the heart, arising from pulmonary artery, with some remarks upon the effect of this anomaly in producing cricoid dilatation of vessel. Journal of anatomy and physiology. 1885; 20:26-9.
- Aykan AC, Yıldız M, Kahveci G, Ozkan M. Two adult cases of anomalous left coronary artery from the pulmonary artery. Turk Kardiyol Dern Ars. 2012;40(1):48-51.
- Liu Y, Miller BW. ALCAPA Presents in an Adult with Exercise Intolerance but Preserved Cardiac Function. Case Reports in Cardiology. 2012;2012:3.
Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
-
Yayımlanma Tarihi
14 Temmuz 2015
Gönderilme Tarihi
23 Haziran 2015
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 2015 Cilt: 2 Sayı: 6