Year 2021 / Volume 113 / Number 7
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Esophageal perforation secondary to an arterial embolization device in scimitar syndrome

541-542

DOI: 10.17235/reed.2021.7832/2021

Patricia Alonso Carnicero, Ibabe Villalabeitia Ateca, Aingeru Sarriugarte Lasarte, Ángel Barturen Barroso,

Abstract
Scimitar syndrome is a congenital malformation that is usually associated with hypoplasia of the right lung with an abnormal blood supply by direct branches of the aorta. These branches normally require embolization.
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References
1- Al Rukban H, Al Ghaihab M, Tamimi O, et al. S. Clinical spectrum ofinfantile scimitar syndrome: A tertiary center experience. Ann Pediatr Cardiol.2014 Jan;7(1):29-33
2- Korkmaz AA, Yildiz CE, Onan B, et al. Scimitar syndrome: a complex form of anomalous pulmonary venous return. J Card Surg. 2011 Sep;26(5):529-34.
3- Silva JC, Braga P, Coutinho D, et al.. Refractory tracheoesophageal fistula management with Amplatzer Occluder placement. Rev Esp Enferm Dig. 2020 Sep;112(9):733-734.
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Alonso Carnicero P, Villalabeitia Ateca I, Sarriugarte Lasarte A, Barturen Barroso Á. Esophageal perforation secondary to an arterial embolization device in scimitar syndrome. 7832/2021


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Publication history

Received: 27/01/2021

Accepted: 05/02/2021

Online First: 25/02/2021

Published: 07/07/2021

Article revision time: 4 days

Article Online First time: 29 days

Article editing time: 161 days


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