Hypertrophic cardiomyopathy after Takeuchi procedure for anomalous origin of the left coronary artery from the pulmonary artery syndrome
Küçük Resim Yok
Tarih
2022
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Wolters Kluwer Medknow Publications
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) syndrome is a rare condition. Surgical intervention is indicated in all diagnosed patients. Successful repair is expected to correct left ventricle (LV) functions and heart failure, reduce mitral regurgitation, and resolve infarct patterns observed on electrocardiogram. For this reason, compared to idiopathic dilated cardiomyopathy, ALCAPA is considered a curable form of dilated cardiomyopathy. In this article, we present the case of 3-month-old girl who underwent the Takeuchi procedure for ALCAPA syndrome and developed hypertrophic cardiomyopathy despite expectations of improved LV function. © 2022 Authors. All rights reserved.
Açıklama
Anahtar Kelimeler
Anomalous origin of the left coronary artery from the pulmonary artery syndrome, hypertrophic cardiomyopathy, Takeuchi procedure, acetylsalicylic acid, digoxin, enalapril, furosemide, propranolol, spironolactone, troponin T, anastomosis, anomalous origin of the left coronary artery from the pulmonary artery syndrome, Article, cardiomegaly, cardiomyopathy, case report, clinical article, computer assisted tomography, congestive cardiomyopathy, electrocardiography, female, heart failure, heart left ventricle function, human, hypertrophic cardiomyopathy, infant, left coronary artery, mitral valve regurgitation, pulmonary artery, Takeuchi procedure, thorax radiography
Kaynak
Annals of Pediatric Cardiology
WoS Q Değeri
Scopus Q Değeri
Q3
Cilt
15
Sayı
5
