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Article type: Research Article
Authors: Hartas, Georgios A. | Gupta-Malhotra, Monesha
Affiliations: Division of Cardiology, Department of Pediatrics, University of Texas Health Science Center, Children's Memorial Hermann Hospital, Houston, TX, Texas
Note: [] Corresponding author: Monesha Gupta-Malhotra MBBS, FAAP, FACC, FASE, Fetal Cardiology, Division of Pediatric Cardiology, University of Texas – Houston Medical School, Children's Memorial Hermann Hospital, 6410 Fannin, UTPB Suite 425, Houston, TX 77030, USA. Tel.: +1 713 500 5743; Fax: +1 713 500 5751; E-mail: [email protected]
Abstract: Presence of systemic venous anomalies including a persistent left superior vena cava to a dilated coronary and interrupted inferior vena cava with azygous continuation are extremely rare in absence of heterotaxia or cardiosplenic syndrome. For this reason, the diagnosis of extracardiac venous anomalies can often be missed in absence of a heterotaxia as was the case in our patient whose prior fetal echocardiogram and the first postnatal echocardiogram read by other pediatric cardiologists failed to detect these anomalies. We report these systemic venous anomalies in a fetus in the absence of heterotaxia and further describe the echocardiographic findings helpful in their detection in-utero.
Keywords: Fetus, echocardiogram, interrupted inferior vena cava, persistent left superior vena cava, azygous vein, congenital cardiac malformation, cardiosplenic syndrome, left atrial isomerism, heterotaxia, systemic venous anomalies
DOI: 10.3233/NPM-2010-0134
Journal: Journal of Neonatal-Perinatal Medicine, vol. 3, no. 4, pp. 337-341, 2010
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