Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2020 / Cilt: 28 - Sayı: 4

Left subclavian artery originating from left pulmonary artery in DiGeorge syndrome

DiGeorge sendromunda sol pulmoner arterden köken alan sol subklavyen arter

Pages
691–694
Publication Date
2022-09-02
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

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.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Left subclavian artery originating from the left pulmonary artery is a rare aortic arch anomaly.
📊
Key Findings & Data:Left subclavian artery originating from the left pulmonary artery is a rare aortic arch anomaly.
💡
Conclusion & Impact: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.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

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.

Özet

Sol pulmoner arterden köken alan sol subklavyen arter, nadir bir arkus aorta anomalisidir. Bu yazıda, Türkiye’de ilk kez, DiGeorge sendromunda duktus arteriyozus ile bağlantılı sol pulmoner arterden köken alan ve subklavyen çalma sendromuna neden olan sol subklavyen arter olgusu sunuldu.

🔖

Cite This Article

GÜLEÇ, E. Y., BORNAUN, H., ERDEM, A., TANG, N. Ç., ALAÇAM, N. Ç. (2022). Left subclavian artery originating from left pulmonary artery in DiGeorge syndrome. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 28 - Sayı: 4, 691–694. https://ajindex.com/articles/423648

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (7)

  1. Momma K. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 2010;105:1617-24.
  2. Abe M, Isobe T, Atsumi N. Right aortic arch with isolation of the left subclavian artery and bilateral patent ductus arterioses. Pediatr Cardiol 2000;21:497-9.
  3. Madan N, Schneider DJ, Jacobs ML. Right aortic arch, isolated left subclavian artery and ductus arteriosus with normal intracardiac anatomy: rare manifestation of chromosome 22q11 deletion. Pediatr Cardiol 2006;27:781-3.
  4. Luetmer PH, Miller GM. Right aortic arch with isolation of the left subclavian artery: case report and review of the literature. Mayo Clin Proc 1990;65:407-13. Edwards JE. Anomalies of the derivatives of the aortic arch system. Med Clin North Am 1948;32:925-49.
  5. Perler BA, Becker GJ, editors. Vascular intervention: A clinical approach. London: Thieme; 1998.
  6. Boztosun B, Avcı A, Saglam M, Meriç M. Coronary subclavian steal syndrome: a case report. Turk Gogus Kalp Dama 2010;18:141-4.
  7. Lee Y, Hong SW. Abnormal origin of the left subclavian artery from the left pulmonary artery in a patient with double outlet right ventricle. Korean J Thorac Cardiovasc Surg 2014;47:32-4