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迪乔治综合征中左锁骨下动脉起源于左肺动脉。

Left subclavian artery originating from left pulmonary artery in DiGeorge syndrome.

作者信息

Çivilibal Tang Nazlıcan, Çelik Alaçam Nida, Bornaun Helen, Erdem Abdullah, Yılmaz Güleç Elif

机构信息

Department of Pediatrics, University of Health Sciences, Kanuni Sultan Süleyman Training and Research Hospital, Istanbul, Turkey.

Department of Pediatric Cardiology, Istanbul Medipol University, Istanbul, Turkey.

出版信息

Turk Gogus Kalp Damar Cerrahisi Derg. 2020 Oct 21;28(4):691-694. doi: 10.5606/tgkdc.dergisi.2020.19613. eCollection 2020 Oct.

DOI:10.5606/tgkdc.dergisi.2020.19613
PMID:33403146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7759048/
Abstract

Left subclavian artery originating from the left pulmonary artery is a rare aortic arch anomaly. Herein, we, for the first time in Turkey, present a case of left subclavian artery originating from the left pulmonary artery via ductus arteriosus in DiGeorge syndrome and causing subclavian steal syndrome.

摘要

起源于左肺动脉的左锁骨下动脉是一种罕见的主动脉弓异常。在此，我们在土耳其首次报告了1例DiGeorge综合征患者，其左锁骨下动脉经动脉导管起源于左肺动脉并导致锁骨下动脉窃血综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/3a81677ab56e/TJTCS-2020-28-4-691-694-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/50706d1abe1f/TJTCS-2020-28-4-691-694-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/0df8341a21a3/TJTCS-2020-28-4-691-694-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/3a81677ab56e/TJTCS-2020-28-4-691-694-F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/50706d1abe1f/TJTCS-2020-28-4-691-694-F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/0df8341a21a3/TJTCS-2020-28-4-691-694-F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de5a/7759048/3a81677ab56e/TJTCS-2020-28-4-691-694-F3.jpg

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本文引用的文献

1
Abnormal origin of the left subclavian artery from the left pulmonary artery in a patient with double outlet right ventricle.一名右心室双出口患者左锁骨下动脉起源于左肺动脉异常。
Korean J Thorac Cardiovasc Surg. 2014 Feb;47(1):32-4. doi: 10.5090/kjtcs.2014.47.1.32. Epub 2014 Feb 5.
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Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.与 22q11.2 缺失综合征相关的心血管异常。
Am J Cardiol. 2010 Jun 1;105(11):1617-24. doi: 10.1016/j.amjcard.2010.01.333.
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Anomalies of the derivatives of the aortic arch system.
主动脉弓系统衍生物的异常。
Med Clin North Am. 1948 Jul;32:925-49. doi: 10.1016/s0025-7125(16)35662-0.
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Right aortic arch, isolated left subclavian artery and ductus arteriosus with normal intracardiac anatomy: rare manifestation of chromosome 22q11 deletion.右位主动脉弓、孤立性左锁骨下动脉及动脉导管，心脏内部结构正常：22q11染色体缺失的罕见表现
Pediatr Cardiol. 2006 Nov-Dec;27(6):781-3. doi: 10.1007/s00246-006-6009-2.
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Right aortic arch with isolation of the left subclavian artery and bilateral patent ductus arterioses.右位主动脉弓伴左锁骨下动脉孤立及双侧动脉导管未闭。
Pediatr Cardiol. 2000 Sep-Oct;21(5):497-9. doi: 10.1007/s002460010121.
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Right aortic arch with isolation of the left subclavian artery: case report and review of the literature.右位主动脉弓伴左锁骨下动脉孤立：病例报告及文献复习
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