Right Ventricle Exclusion in Severe Neonatal Ebstein's Anomaly / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
;
: 518-521, 2010.
Artigo
em 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:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Circulação Pulmonar
/
Sopros Cardíacos
/
Atresia Pulmonar
/
Técnica de Fontan
/
Cianose
/
Permeabilidade do Canal Arterial
/
Anomalia de Ebstein
/
Procedimento de Blalock-Taussig
/
Átrios do Coração
/
Ventrículos do Coração
Limite:
Humanos
Idioma:
Coreano
Revista:
The Korean Journal of Thoracic and Cardiovascular Surgery
Ano de publicação:
2010
Tipo de documento:
Artigo
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