Kelainan Kongenital Tidak Terbentuknya Arteri Koroner Kiri Utama, dan Sumber Left Anterior Descending Coronary Artery Berasal dari Sinus Aorta Kanan.

Authors

  • fatimah shahab Mataram university

DOI:

https://doi.org/10.29303/jku.v11i2.665

Keywords:

Anomali arteri koroner, Tidak terbentuknya LMCA, Anomali origin.

Abstract

Congenital coronary artery anomalies are rare. Clinically, coronary artery anomalies can be benign or life-threatening depending on the prognosis. This case report aims to describe a patient who presented with atypical chest pain as an early symptom who underwent CT scan. The CT scan image showed total calcium score 0, anomalous origin of the LAD from the right aortic sinus, and no evidence of plaque or stenosis at LM, LAD, LCX, RCA. This anomaly is included in the classification of  anomalous origin. LAD originates from the right aortic sinus, with a pre-pulmonic pathway so that the hemodynamics is still good and is classified as an anomaly without ischemia.

 

Keywords: Coronary artery anomaly, Absence of LMCA, Anomalous origin.

References

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2. Ajayi NO, Lazarus L, Vanker EA, Satyapa K. 2015. Absent Left Main Coronary Artery with Variation in the Origin of its Branches in a South African Populatio. Anat. Histol. Embryol. 44 (2015) 81–85. doi: 10.1111/ahe.12109
3. Angelini P. 2007. Coronary Artery Anomalies. Circulation. 2007;115:1296-1305. DOI: 10.1161/CIRCULATIONAHA.106.618082
4. Villa DM, Sammut E, Nair A, Rajani R, Bonamini, Chiribiri.2016. Coronary artery anomalies overview: The normal and the abnormal. World J Radiol 2016 June 28; 8(6): 537-555 ISSN 1949-8470 (online). DOI: 10.4329/wjr.v8.i6.537.
5. Siharini J. 2018. Isolated Coronary Artery Anomalies. Available at: https://emedicine.medscape.com/article/153512

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Published

2022-06-30

How to Cite

shahab, fatimah. (2022). Kelainan Kongenital Tidak Terbentuknya Arteri Koroner Kiri Utama, dan Sumber Left Anterior Descending Coronary Artery Berasal dari Sinus Aorta Kanan. Jurnal Kedokteran, 11(2), 866–869. https://doi.org/10.29303/jku.v11i2.665

Issue

Section

Case Report

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