Management of Pentalogy of Cantrell with complete ectopia cordis and Double Outlet Right Ventricle
نویسندگان
چکیده
منابع مشابه
Pentalogy of Cantrell Associated With Thoracoabdominal Ectopia Cordis
A 4-day-old female infant with a partially extrathoracic heart in her supraumbilical abdominal wall (Figure 1A) presented with symptoms of tachypnea and mild cyanosis. Physical examination showed a thoracoabdominal wall defect with thoracoabdominal ectopia cordis. The xyphoid was absent and the sternum was short. Oxygen room air saturation was 85%. Chest x-ray showed dextrocardia and descensus ...
متن کامل[Cardiac malformations in patients with pentalogy of Cantrell and ectopia cordis].
We studied 21 patients who presented with a diagnosis of pentalogy of Cantrell. Their mean age was 40 days. All patients presented with congenital heart disease. Six presented with ectopia cordis. Every patient was subjected to echocardiography. Double outlet right ventricle, an atrial septal defect and dextrocardia were seen in 5 patients (24%). Four patients survived. Seventeen died, 12 from ...
متن کاملImages in cardiovascular medicine: Pentalogy of Cantrell associated with thoracoabdominal ectopia cordis.
A 4-day-old female infant with a partially extrathoracic heart in her supraumbilical abdominal wall (Figure 1A) presented with symptoms of tachypnea and mild cyanosis. Physical examination showed a thoracoabdominal wall defect with thoracoabdominal ectopia cordis. The xyphoid was absent and the sternum was short. Oxygen room air saturation was 85%. Chest x-ray showed dextrocardia and descensus ...
متن کاملdouble-outlet right ventricle
In a previous study the possibility that tetralogy of Fallot and transposition of the great arteries may arise as a result of embryonic arrests in the normal rotation of the junction of the outflow tract and the great arteries was investigated. The results suggested that the development of other transposition complexes such as double-outlet right ventricle might also be related to arrests in th...
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ژورنال
عنوان ژورنال: Congenital Anomalies
سال: 2015
ISSN: 0914-3505
DOI: 10.1111/cga.12096