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Clinical case of congenital heart disease: aorta arc break

https://doi.org/10.25789/YMJ.2020.71.33

Abstract

Aortic arch interruption (AAI) is a rare congenital anomaly characterized by the absence of one of the segments of the aortic arch with a violation of its continuity and the ductus-dependent nature of the blood flow through the descending aorta. In this article, we present a clinical case of AAI in a child born in 2019 and examined at the Perinatal Center of “Republican Hospital №1 - National Medical Center”.

Timely diagnosis of AAI, conservative treatment for preoperative stabilization of the child’s condition allowed positive solving the question of surgical treatment in Novosibirsk cardiac surgery center.

About the Authors

S. N. Alekseeva
РБ №1-НЦМ
Russian Federation


V. B. Egorova
МИ СВФУ им. М.К. Аммосова
Russian Federation


I. P. Govorova
РБ №1-НЦМ
Russian Federation


V. M. Konstantinova
РБ №1-НЦМ
Russian Federation


N. I. Douglas
МИ СВФУ им. М.К. Аммосова
Russian Federation


S. B. Ksenofontova
МИ СВФУ им. М.К. Аммосова
Russian Federation


References

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2. Zatikyan EP. Cardiology of the fetus / E.P. Zatikyan. – M.: Triad-X, 2009. - 216 p.

3. Saidova V.T. Early detection of critical congenital heart defects in newborns using NT-proBNP / V.T. Saidova D.R. Sabirova, E.M. Nemirovskaya, L.M. Mirolyubov // Practical medicine. – 2013. – Vol. 6 (75). – P. 144-146.

4. Sokolov A.A. Comparison of the results of fetal and postnatal echocardiography / A.A. Sokolov, G.I. Martsinkevich // Russian Bulletin of Perinatology and Pediatrics. – 2014. – Vol. 59 (3). – P. 66-70.

5. Yalynskaya T.A. Aortic arch interruption: diagnosis of malformation by multidetector computed tomography / T.A. Yalinskaya // Promeneva diagnostics, promeneva therapy. – 2012. – Vol. 4. – P. 17-20


Review

For citations:


Alekseeva S.N., Egorova V.B., Govorova I.P., Konstantinova V.M., Douglas N.I., Ksenofontova S.B. Clinical case of congenital heart disease: aorta arc break. Yakut Medical Journal. 2020;(3):131-133. (In Russ.) https://doi.org/10.25789/YMJ.2020.71.33

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ISSN 1813-1905 (Print)
ISSN 2312-1017 (Online)