Background: Left ventricular to right
atrial communications (LV-RA) or the Gerbode defects are rare and complex types
of ventricular septal defect. Their clinical diagnosis is not specific.
However, the main clue to identifying Gerbode defect comes
fromDoppler-coupled echocardiography (TTE), and the treatment is mainly surgical. Aim:We hereby
report our experience in surgical management of Gerbode defect through two exceptional congenital cases
(type 1 and type 2 of Gerbode defect). CasePresentation: The diagnosis was established in adult patients, the first case is a 27-year-old woman who
had dyspnea, and in whom the TTE
revealed LV-RA communication, with repercussions on the right cavities.
The second case is a 23-year-oldman, with the concept of
statutory weight delay, consulted for progressive dyspnea; the TTE initially revealed a very large perimembranous
ventricular defect associated with
significant pulmonary hypertension. Cardiopulmonary bypass surgery was done for a successful and complete correction.
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