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.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Artère pulmonaire
/
Malformations
/
Coronarographie
/
Maladie coronarienne
/
Vaisseaux coronaires
/
Dépression
/
Électrocardiographie
/
Syndrome de Bland-White-Garland
/
Cardiopathies congénitales
/
Défaillance cardiaque
Limites du sujet:
Adolescent
/
Adulte
/
Enfant
/
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Medicine
Année:
2005
Type:
Article
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