Ebstein's anomaly in persistent common atrioventricualr canal
Autor: | T G Losekoot, G Caruso, Anton E. Becker |
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Rok vydání: | 1978 |
Předmět: |
Male
medicine.medical_specialty Internal medicine Ebstein's anomaly Deformity medicine Humans cardiovascular diseases Angiocardiography Heart septal defect medicine.diagnostic_test business.industry Heart Septal Defects Infant Newborn Infant medicine.disease Infant newborn Ebstein Anomaly Child Preschool cardiovascular system Cardiology Atrioventricular canal Female Persistent atrioventricular canal Abnormality medicine.symptom Cardiology and Cardiovascular Medicine business Research Article |
Zdroj: | Heart. 40:1275-1279 |
ISSN: | 1355-6037 |
DOI: | 10.1136/hrt.40.11.1275 |
Popis: | This report documents 2 patients who presented with cyanosis early in life. In both instances the necropsy showed the simultaneous occurrence of an imcomplete type of persistent atrioventricular canal and an Ebstein's malformation of the "tricuspid" valve component. In the first patient no clinical investigations were done. In the second patient the electrocardiogram was consistent with persistent atrioventricular canal and the angiocardiogram showed the characteristic goose-neck deformity. Moreover, an abnormality of the right cardiac contour was seen, which in retrospect was correlated with the right-sided Ebstein's malformation. Ebstein's anomaly may significantly alter the clinical and haemodynamic profile of atrioventricular canal and should be considered in atypical cases. The presence of Ebstein's anomaly will complicate surgical repair of the atrioventricular canal. |
Databáze: | OpenAIRE |
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