Surgical Repair for Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery
Korean Circulation Journal
; : 144-147, 2017.
Article
en En
| WPRIM
| ID: wpr-121550
Biblioteca responsable:
WPRO
ABSTRACT
Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a very rare congenital heart defect. Herein, we describe three cases of ARCAPA in an 8 months old, 18 months old, and 4 year old child. Two cases were incidentally diagnosed using a computed tomographic angiograph, and the other was incidentally diagnosed using a coronary angiograph. These cases underwent a reimplantation technique on diagnosis and resulting in positive clinical outcomes during the follow-up period which was a mean of 1.5 years.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Arteria Pulmonar
/
Reimplantación
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Anomalías Congénitas
/
Estudios de Seguimiento
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Anomalías de los Vasos Coronarios
/
Vasos Coronarios
/
Diagnóstico
/
Electrocardiografía
/
Cardiopatías Congénitas
/
Procedimientos Quirúrgicos Cardíacos
Tipo de estudio:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Límite:
Child
/
Humans
Idioma:
En
Revista:
Korean Circulation Journal
Año:
2017
Tipo del documento:
Article