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Date Published:
30/03/2023
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Nguyễn, Đình M. ., & Trịnh , A. T. . (2023). CONGENITAL ABSENCE OF LEFT CIRCUMFLEX ARTERY: A CASE REPORT. Vietnam Medical Journal, 524(2). https://doi.org/10.51298/vmj.v524i2.4838
CONGENITAL ABSENCE OF LEFT CIRCUMFLEX ARTERY: A CASE REPORT
Main Article Content
Abstract
Congenital absence of left circumflex artery is a rare coronary malformation with few reported cases in the literature. The risk of stroke can occur when the patient on exertion. Most cases are discovered incidentally during coronary percutaneous angiography or computed tomography angiography. We report 2 cases incidentally discovered congenital absence of left circumflex artery and dominant right coronary artery on 256-slices CT. Thereby, we would like to review the literature on clinical manifestations and diagnostic methods also managements of this anomaly in the article.
Article Details
Keywords
LCX, absence of left LCX, 256-slices MSCT.
References
1. Saad Ullah, Muzammil Khan, Noman Ahmed Jang Khan và các cộng sự. (2017). Absence of Left Circumflex Artery: A Rare Congenital Disorder of Coronary Arteries. Case Reports in Cardiology, 2017, 8710135.
2. Setri Fugar, Lydia Issac, Alexis Kofi Okoh và các cộng sự. (2017). Congenital Absence of Left Circumflex Artery: A Case Report and Review of the Literature. Case reports in cardiology, 2017, 6579847-6579847.
3. D. Varela, M. Teleb, S. Said và các cộng sự. (2015). Congenital Absence of Left Circumflex Presenting After an Emotional Stressor. Pol J Radiol, 80, 529-31.
4. Marcos Danillo Peixoto Oliveira, Fernando Roberto de Fazzio, José Mariani Junior và các cộng sự. (2015). Superdominant Right Coronary Artery with Absence of Left Circumflex and Anomalous Origin of the Left Anterior Descending Coronary from the Right Sinus: An Unheard Coronary Anomaly Circulation. Case Reports in Cardiology, 2015, 721536.
5. P. Jariwala, K. Jadhav và S. S. Kale. (2021). Congenital absence of the left circumflex artery: Case series and review. Asian Cardiovasc Thorac Ann, 29(8), 826-835.
6. Y. Majid, M. Warade, J. Sinha và các cộng sự. (2011). Superdominant right coronary artery with absent left circumflex artery. Biomed Imaging Interv J, 7(1), e2.
7. S. S. A. Shaikh, V. Deshmukh, V. Patil và các cộng sự. (2018). Congenital Absence of the Left Circumflex Artery With Super-Dominant Right Coronary Artery: Extremely Rare Coronary Anomaly. Cardiol Res, 9(4), 264-267.
8. O. Ince, K. Gülşen, S. Tuğrul và các cộng sự. (2020). Congenital absence of the left circumflex artery in a patient presenting with acute inferior myocardial infarction. Anatol J Cardiol, 24(4), E11-e12.
2. Setri Fugar, Lydia Issac, Alexis Kofi Okoh và các cộng sự. (2017). Congenital Absence of Left Circumflex Artery: A Case Report and Review of the Literature. Case reports in cardiology, 2017, 6579847-6579847.
3. D. Varela, M. Teleb, S. Said và các cộng sự. (2015). Congenital Absence of Left Circumflex Presenting After an Emotional Stressor. Pol J Radiol, 80, 529-31.
4. Marcos Danillo Peixoto Oliveira, Fernando Roberto de Fazzio, José Mariani Junior và các cộng sự. (2015). Superdominant Right Coronary Artery with Absence of Left Circumflex and Anomalous Origin of the Left Anterior Descending Coronary from the Right Sinus: An Unheard Coronary Anomaly Circulation. Case Reports in Cardiology, 2015, 721536.
5. P. Jariwala, K. Jadhav và S. S. Kale. (2021). Congenital absence of the left circumflex artery: Case series and review. Asian Cardiovasc Thorac Ann, 29(8), 826-835.
6. Y. Majid, M. Warade, J. Sinha và các cộng sự. (2011). Superdominant right coronary artery with absent left circumflex artery. Biomed Imaging Interv J, 7(1), e2.
7. S. S. A. Shaikh, V. Deshmukh, V. Patil và các cộng sự. (2018). Congenital Absence of the Left Circumflex Artery With Super-Dominant Right Coronary Artery: Extremely Rare Coronary Anomaly. Cardiol Res, 9(4), 264-267.
8. O. Ince, K. Gülşen, S. Tuğrul và các cộng sự. (2020). Congenital absence of the left circumflex artery in a patient presenting with acute inferior myocardial infarction. Anatol J Cardiol, 24(4), E11-e12.