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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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2023, Number 2

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Cir Card Mex 2023; 8 (2)

Berry syndrome: One-Stage Surgical Repair

Yagual-Gutiérrez E, García-Mora R, De La Cruz-Rodríguez L, Bautista-Ramírez TZ, Ortega-Zhindón DB, Cervantes-Salazar JL
Full text How to cite this article

Language: English
References: 9
Page: 41-44
PDF size: 261.09 Kb.


Key words:

Aortopulmonary window, Anomalous implantation of the right pulmonary artery, Berry syndrome, Congenital malformation, Interruption of the aortic arch, 3D vascular reconstruction.

ABSTRACT

Berry Syndrome is characterized by the sum of several abnormalities; namely, aortopulmonary window, aortic origin of the right pulmonary branch, interruption of the aortic arch and intact interventricular septum. First described by Berry et al. in 1982. We present the case of a 21-day-old infant weighing 3.3kg, with a progressive increase in respiratory effort, vomiting, and irritability. Complementary studies were carried out reporting the anomalies that make up the Berry Syndrome.


REFERENCES

  1. Bi WJ, Xiao YJ, Liu YJ, Hou Y, Ren WD. Berry syndrome: a case report andliterature review. BMC Cardiovasc Disord. 2021;21(1):15. doi: 10.1186/s12872-020-01837-y.

  2. Park SY, Joo HC, Youn YN, Park YH, Park HK. Berry syndrome: two cases ofsuccessful surgical repair. Circ J. 2008;72(3):492-5. doi: 10.1253/circj.72.492.

  3. Habibie YA, Busro PW, Roebiono PS, Fakhri D. Berry syndrome; a successfulone-stage repair in neonate periods, evaluation result after 9 years, a case report.Ann Med Surg (Lond). 2021;64:102200. doi: 10.1016/j.amsu.2021.102200.

  4. Shi XC, Weng JB, Yu J, Ma XH, Pu YQ, Ying LY, Yu JG. Outcomes of One-Stage Surgical Repair for Berry Syndrome in Neonates. Front Cardiovasc Med.2022;8:790303. doi: 10.3389/fcvm.2021.790303.

  5. Berry TE, Bharati S, Muster AJ, et al. Distal aortopulmonary septal defect, aorticorigin of the right pulmonary artery, intact ventricular septum, patent ductus arteriosusand hypoplasia of the aortic isthmus: a newly recognized syndrome. Am JCardiol. 1982;49:108–16. doi: 10.1016/0002-9149(82)90284-3.

  6. Yoo SJ, Choi HY, Park IS, Hong CY, Song MG, Kim SH. Distal aortopulmonarywindow with aortic origin of the right pulmonary artery and interruption of theaortic arch (Berry syndrome): diagnosis by MR imaging. AJR Am J Roentgenol.1991;157(4):835-6. doi: 10.2214/ajr.157.4.1892045.

  7. Choi CH, Kim WH, Kwak JG, et al. One stage repair of Berry syndrome in aneonate. Korean J Thorac Cardiovasc Surg 2004; 37: 918 – 921.

  8. Hu R, Zhang W, Liu X, Dong W, Zhu H, Zhang H. Current outcomes of onestagesurgical correction for Berry syndrome. J Thorac Cardiovasc Surg.2017;153(5):1139-1147. doi: 10.1016/j.jtcvs.2016.11.058.

  9. Binsalamah ZM, Greenleaf CE, Heinle JS. Type A interrupted aortic arch and typeIII aortopulmonary window with anomalous origin of the right pulmonary arteryfrom the aorta. J Card Surg. 2018;33(6):344-347. doi: 10.1111/jocs.13717.




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Cir Card Mex. 2023;8