Case report of rare congenital cardiovascular anomalies associated with truncus arteriosus type 2
Leona S. Alizadeh,
Vitali Koch,
Leon D. Grünewald,
Ibrahim Yel,
Daniel Mathies,
Dominic Rauschning,
Thomas J. Vogl,
Christian Booz
Affiliations
Leona S. Alizadeh
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Department of Diagnostic and Interventional Radiology, Bundeswehrzentralkrankenhaus Koblenz, Koblenz, Germany; Corresponding author.
Vitali Koch
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany
Leon D. Grünewald
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany
Ibrahim Yel
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany
Daniel Mathies
Department of Internal Medicine, Bundeswehrzentralkrankenhaus Koblenz, Koblenz, Germany
Dominic Rauschning
Department of Internal Medicine, Bundeswehrzentralkrankenhaus Koblenz, Koblenz, Germany
Thomas J. Vogl
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany
Christian Booz
Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany; Division of Experimental Imaging, Department of Diagnostic and Interventional Radiology, University Hospital Frankfurt, Germany
Truncus arteriosus (TA) is a very rare congenital anomaly with complex cardiovascular anatomy and high lethality also due to severe associated anatomical variants and pathologies. As TA has a massive impact on the survival of a newborn and usually has to be surgically treated. Thus, it is of high importance to understand this congenital cardiovascular disease and associated complications, to improve life expectancy and outcome of these patients. We recently came across a newborn female patient with a rare complex case of persistent TA type 2 associated with further complex cardiovascular anomalies, who received a contrast enhanced CT scan on the 3 rd day post-partum, showing complex cardiovascular abnormalities that were ultimately incompatible with life.