已发表论文

产后主动脉弓闭锁一例

 

Authors Yang ZX, Han Y, Zhang J, Yu YH, Zhu M

Received 18 July 2023

Accepted for publication 12 September 2023

Published 26 September 2023 Volume 2023:16 Pages 4265—4270

DOI https://doi.org/10.2147/JIR.S428231

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Professor Ning Quan

Background: Aortic arch atresia is a rare congenital cardiac defect that may occur after birth. Pregnant women with gestational diabetes mellitus may increase the risk of aortic arch atresia in newborns after birth.
Case Description: A 16-day-old infant was referred to our hospital on the 15th postnatal day after an interrupted or atretic aortic arch was discovered. No obvious abnormality was detected in the infant during the prenatal ultrasound. Laboratory tests showed elevated inflammatory marker levels. Transthoracic echocardiography showed stenosis of the transverse arch of the aorta and a blind end at the distal end of the left subclavian artery. During surgery, it was found that the isthmus of the aorta was uninterrupted but completely occluded due to inflammation.
Conclusion: This case demonstrates that type A interrupted aortic arch and coarctation of the aorta can be acquired after birth, and if coarctation of the aorta is complicated by inflammation or if the pregnant women have gestational diabetes mellitus, it can result in aortic arch atresia as the patient’s condition worsens. It is advised to consider aortic arch atresia when imaging reveals type A interrupted aortic arch.
Keywords: aortic arch atresia, congenital heart disease, congenital obstruction and anomaly of the aortic arch, gestational diabetes mellitus