Key result
Uhl's anomaly of the right ventricle in a 1-year-old male child with severe right ventricular dilation and poor function defied surgical options and required a heart transplant recommendation.
Why the study?
Uhl's anomaly of the right ventricle is a very rare condition with limited reported cases and no satisfactory surgical options except transplant.
Case Report (n=1)
Answers are grounded in this paper and cite their sources.
Heart transplant may be warranted when surgery fails in severe infantile Uhl's anomaly; leaves open optimal strategies given extreme rarity.
Uhl's anomaly of the right ventricle is a rare anomaly. At present, only about 84 cases have been reported in over a century. We report a case of a 1-year-old male child who presented to our outpatient pediatric cardiology clinic with a history of recurrent cough and difficulty in breathing and failure to gain weight in the preceding 2 months. Chest X-ray showed cardiomegaly, whereas electrocardiogram showed a normal sinus rhythm with poor right ventricular (RV) forces. Echocardiography showed severely dilated right ventricle with thinned out right ventricle wall and poor RV function with severe tricuspid regurgitation. He has been placed on aspirin, lasilactone, and clexane. However, there was no satisfactory surgical option available, and heart transplant was recommended. Uhl's anomaly of the right ventricle is a very rare anomaly which defies all surgical option except transplant. Early recognition institution of drugs that improves cardiac function may improve the quality of life of the child.
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Chinawa et al. (2017) conducted a case report in Uhl's anomaly of the right ventricle (n=1). Heart transplantation was evaluated. Uhl's anomaly of the right ventricle in a 1-year-old male child with severe right ventricular dilation and poor function defied surgical options and required a heart transplant recommendation.
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