Scimitar Syndrome and H-type Tracheo-esophageal Fistula in a Newborn Infant.

Autor:	Lastinger A; Department of Pediatrics-Internal Medicine, WVU School of Medicine, Morgantown, WV 26505, USA., El Yaman M; Department of Pediatrics, WVU School of Medicine, Morgantown, WV 26505, USA., Gustafson R; Department of Pediatric Cardiovascular and Thoracic Surgery, WVU School of Medicine, Morgantown, WV 26505, USA., Yossuck P; Department of Pediatrics-Internal Medicine, WVU School of Medicine, Morgantown, WV 26505, USA. Electronic address: pyossuck@hsc.wvu.edu.
Jazyk:	angličtina
Zdroj:	Pediatrics and neonatology [Pediatr Neonatol] 2016 Jun; Vol. 57 (3), pp. 236-9. Date of Electronic Publication: 2013 Oct 23.
DOI:	10.1016/j.pedneo.2013.06.010
Abstrakt:	Scimitar syndrome is a rare congenital anomaly characterized by partial anomalous pulmonary venous drainage of the right lung to the inferior vena cava (IVC) creating a tubular opacity paralleling the right cardiac border on chest radiography which resembles a curved Turkish sword or scimitar. Associated pulmonary and vascular anomalies have been reported in cases of Scimitar syndrome, most commonly hypoplasia of right lung, dextroposition of the heart, hypoplasia of the right pulmonary artery, and aberrant arterial supply from the descending aorta to the affected lobe of the right lung. To the best of our knowledge, this is the first case of Scimitar syndrome with an H-type tracheoesophageal fistula that has ever been reported. (Copyright © 2013. Published by Elsevier B.V.)
Databáze:	MEDLINE
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