Right Ventricle Exclusion in Severe Neonatal Ebstein's Anomaly / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
;
: 518-521, 2010.
Artículo
en Coreano
| WPRIM
| ID: wpr-196948
ABSTRACT
A one-day-old baby was transferred for cyanosis and heart murmur. Echocardiographic evaluation revealed that he had severe neonatal Ebstein's anomaly (Carpentier type C), pulmonary atresia, and pulmonary circulation via patent ductus arteriosus. Because the wall of the atrialized right ventricle was very thin, showed decreased contractility, and the small right ventricle showed pulmonary atresia, we decided that a two-ventricular repair was impossible. When the patient was one-month-old, he underwent right atrium reduction-plasty, a right ventricular exclusion procedure (including atrialized right ventricle resection and functional right ventricle plication), and right modified Blalock-Taussig shunt. He was discharged without specific problems. He received a bidirectional cavopulmonary shunt successfully at 4 months later.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Circulación Pulmonar
/
Soplos Cardíacos
/
Atresia Pulmonar
/
Procedimiento de Fontan
/
Cianosis
/
Conducto Arterioso Permeable
/
Anomalía de Ebstein
/
Procedimiento de Blalock-Taussing
/
Atrios Cardíacos
/
Ventrículos Cardíacos
Límite:
Humanos
Idioma:
Coreano
Revista:
The Korean Journal of Thoracic and Cardiovascular Surgery
Año:
2010
Tipo del documento:
Artículo
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