ALCAPA syndrome in an asymptomatic young soccer player

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Atıf İçin Kopyala

RAMOĞLU M. G., Bulut M. O., Epcacan S., Dedemoglu M.

TURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, cilt.27, sa.3, ss.388-391, 2019 (SCI-Expanded)

• Yayın Türü: Makale / Tam Makale
• Cilt numarası: 27 Sayı: 3
• Basım Tarihi: 2019
• Doi Numarası: 10.5606/tgkdc.dergisi.2019.16320
• Dergi Adı: TURK GOGUS KALP DAMAR CERRAHISI DERGISI-TURKISH JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
• Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
• Sayfa Sayıları: ss.388-391
• Anahtar Kelimeler: ALCAPA, asymptomatic, coronary anomaly, left heart failure, LEFT CORONARY-ARTERY, ANOMALOUS ORIGIN
• Ankara Üniversitesi Adresli: Evet

Özet

Anomalous origin of left coronary artery from pulmonary artery syndrome is a rare, but severe congenital cardiac malformation. It is an important cause of dilated cardiomyopathy and left heart failure during infancy and, if left untreated, the prognosis is poor with an overall mortality rate over 90%. About 15% of patients can survive beyond the first year of life, depending on the development of collateral circulation and may present with angina, dyspnea, syncope, and arrhythmias. Myocardial infarction and sudden cardiac death may be the only and the first symptom in some cases. The treatment of choice for this syndrome is urgent surgical intervention with favorable long-term outcomes. Herein, we present an asymptomatic adolescent active sportsman who was diagnosed with anomalous origin of left coronary artery from pulmonary artery syndrome and underwent a successful surgery.