Background: Double chambered right ventricle (DCRV) is a relatively rare congenital heart disease, characterized by the abnormal division of the right ventricle into a high-pressure inlet and low-pressure outlet by anomalous muscle bundles. Extra-cardiac right-to-left shunts may present with clinical symptoms in adulthood and should be sought in patients with previous cavo-pulmonary shunt procedures. Case presentation. We report a case of DCRV in a 29 year old Caucasian male presenting in adulthood with a right-to-left shunt secondary to venous collaterals, following cavopulmonary anastomosis for congenital pulmonary atresia and hypoplastic right ventricle. Conclusion: Multimodality cardiac imaging using echocardiography, cardiac CT, cardiac MRI and cardiac catheterization is often required for complete characterization of complex congenital heart anomalies in adulthood. © 2012 Kha et al.; licensee BioMed Central Ltd.
CITATION STYLE
Kha, L. C., Cassano-Bailey, A., Cleverley, K., Sud, M., Strzelczyk, J., & Jassal, D. S. (2012). Multimodality cardiac imaging of a double chambered right ventricle with intrapulmonary shunting: A case report. BMC Research Notes, 5. https://doi.org/10.1186/1756-0500-5-516
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