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Surgical Rrepair of Ebsteins Anomaly with Ventricular Septal Defect in the Infant  

유지훈 (성균관대학교 의과대학 삼성서울병원 흉부외과)
박표원 (성균관대학교 의과대학 삼성서울병원 흉부외과)
성기익 (성균관대학교 의과대학 삼성서울병원 흉부외과)
박계현 (성균관대학교 의과대학 삼성서울병원 흉부외과)
이영탁 (성균관대학교 의과대학 삼성서울병원 흉부외과)
전태국 (성균관대학교 의과대학 삼성서울병원 흉부외과)
Publication Information
Journal of Chest Surgery / v.35, no.12, 2002 , pp. 890-893 More about this Journal
Abstract
Ebsteins anomaly is a rare congenital cardiac malformation that is the downward displacement of the septal and posterior leaflets of the tricuspid valve into the ventricular apex, aresulting in the formation of an atrialized portion of the right ventricle. In most patients, symptoms such as cyanosis and progressive heart failure occur during the adolescence or young adulthood. The associated anomalies include ventricular septal defect, transposition of the great arteries, and malformation of the mitral valve. An 8-months-old male with Ebsteins anomaly, ventricular septal defect, and duplication of the mitral valve orifice successfully underwent operation with VSD patch closure. Postoperatively, cardiac size was significantly reduced and tricuspid regurgitation was trivial in echocardiography He has been doing well without any cardiac medication during the 18 months follow up after operation.
Keywords
Ebstein′s anomaly; Infant;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
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