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Cirugía Cardiaca en México

ISSN 2448-5640 (Print)
Diario Oficial de la Sociedad Mexicana de Cirugía Cardiaca, A.C., y del Colegio Mexicano de Cirugía Cardiovascular y Torácica, A.C.
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2019, Number 4

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Cir Card Mex 2019; 4 (4)

Double aortic arch. Case report

Espinosa-Blanco O, Gómez-Martínez L, Medina-Escobedo SG, Landín-Robles R
Full text How to cite this article

Language: English
References: 4
Page: 120-122
PDF size: 195.55 Kb.


Key words:

Aorta, Congenital heart disease, Double aortic arch, Vascular ring.

ABSTRACT

Double aortic arch is a rare pathology but it is the most frequent variant of a complete vascular ring. It occurs when the ascending aorta bifurcates into two arches, one posterior right and the other anterior left. Both arches surround the trachea and esophagus and converging into descending aorta. For all the above, respiratory or digestive symptoms could appear. Management is basically surgical. We report the case of a pediatric patient with double aortic arch successfully treated by surgery.


REFERENCES

  1. Priya S, Thomas R, Magpal P, Sharma A, Steigmer M. Congenital anomalies ofthe aortic arch. Cardiovasc Diagn Ther. 2018;8(Suppl 1):S26-S44.

  2. Nagre SW, Kulkarni DV. Double aortic arch surgery. Indian J Vasc Endovasc Surg2015;2:118-21.

  3. Woods R, Ronald J, Holcomb G, Snyder C, Loflnd G, Ashcraft K, Holder T. VascularAnomalies and Tracheoesophageal Compression: A Single Institution’s 25-Year Experience. Ann Thorac Surg 2001;72:434 –9.

  4. Chun K, Colombani P, Dudgeon D, Haller A. Diagnosis and Management of CongenitalVascular Rings: A 22-Year Experience. Ann Thorac Surg 1992;53:597-603




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Cir Card Mex. 2019;4