A case of anomalous origin of left coronary artery from the pulmonary artery: Report of an adult case / 대한내과학회지
Korean Journal of Medicine
;
: 566-570, 2005.
Artigo
em Coreano
| WPRIM
| ID: wpr-156624
ABSTRACT
Anomalous origin of the left coronary artery from pulmonary artery was first described in a child by Brooks. This ALCAPA syndrome is a rare congenital anomaly occuring in approximately 0.25~0.50% of children having congenital heart disease. Although approximately 80 to 90% of patients develop congestive heart failure and die in infancy, some pateints may present this syndrome in adolescents or adults. This anomaly was detected during elective coronary angiogram in a 63 year-old female patient with typical angina. Down-sloping ST depression was demonstrated on exercise stress ECG. Coronary angiogram and pulmonary angiogram revealed an anomalous origin of left coronary artery from pulmonary artery.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Artéria Pulmonar
/
Anormalidades Congênitas
/
Angiografia Coronária
/
Doença das Coronárias
/
Vasos Coronários
/
Depressão
/
Eletrocardiografia
/
Síndrome de Bland-White-Garland
/
Cardiopatias Congênitas
/
Insuficiência Cardíaca
Limite:
Adolescente
/
Adulto
/
Criança
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Medicine
Ano de publicação:
2005
Tipo de documento:
Artigo
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