Abstract
Background
Quadfurcation of single coronary artery (SCA) from the right is an extremely rare anomaly and acute coronary syndrome in such patients is catastrophic.
Case summary
We report a 56-year-old Bangladeshi male who presented with an acute inferior wall ST-elevation myocardial infarction. He was taken to the Cath lab for primary percutaneous coronary intervention which showed the presence of SCA arising from the right aortic sinus with multiple lesions including a bifurcation lesion. Percutaneous coronary intervention was done successfully in two sessions.
Discussion
Tackling multiple lesions in a case of SCA with quadfurcation was challenging especially in the setting of SCA and bifurcation lesions. This is first reported case of this kind.
Keywords: Single coronary artery, ST-elevation myocardial infarction, Trishul, Percutaneous coronary intervention, Quadfurcation, Case report
Learning points
Quadfurcation of single coronary artery from the right is extremely rare anomaly.
Always activate heart team while managing such patients for a better outcome and treatment strategy.
During coronary angiogram always look for associated congenital anomalies.
The use of 5-Fr catheter is advisable as majority cases have done successfully without any complications. We have treated the patient with the help of 6-Fr catheter without any complications and the choice should be left to the interventional cardiologist.
Introduction
Single coronary artery (SCA) is a condition in which the entire left coronary arterial system arises from right coronary sinus.1 Among the congenital coronary anomalies, SCA arising from the right aortic cusp is rare with a prevalence during coronary angiogram between 0.02% and 0.05%.2
Timeline
28 August 2016 | Presented to emergency room as case ST-elevation in myocardial infarction. |
28 August 2016 | Single coronary artery arising from the right was noted. Primary percutaneous coronary intervention is done to proximal right coronary artery, ostial right posterior descending artery, and right posterior atrioventricular artery with one drug eluting stent in each artery. |
30 August 2016 | Staged angioplasty was done to first obtuse marginal and to proximal left circumflex coronary artery. |
1 September 2016 | Discharged with appointment for computed tomography coronary angiogram. |
13 October 2016 | Contrast-enhanced multidetector computed tomography 64 slices coronary angiogram was performed. |
Case presentation
A 56-year-old Bangladeshi male with no prior medical history presented with an inferior wall ST-elevation myocardial infarction with Killip Class II (Figure 1). The cardiopulmonary examination was normal and the total ischaemic time was 90 min.
Baseline laboratory investigations showed hs-Troponin-i ≥100 ng/mL (Ref. range: 0.01–0.04 ng/mL). Urgent cardiac catheterization was performed which revealed the presence of an SCA arising from the right aortic sinus which quadfurcated into left anterior descending (LAD) coronary artery, first diagonal (D1), left circumflex coronary artery (LCx), and right coronary artery (RCA).
Multiple atherosclerotic lesions were present with 70–90% stenosis in the distal LAD and a severely calcified 70–90% stenosis in the D1 with reference diameter of the vessel at this level less than 1.5 mm. About 70–90% stenosis was present in the proximal circumflex (LCx) and had a 90–99% stenosis in the first obtuse marginal (OM1). Proximal RCA had an acute occlusion (Figure 2). The crux of the RCA had a bifurcation lesion with MEDINA (0,1,1) of 90–99% (Supplementary material online, Video S1). Percutaneous coronary intervention (PCI) was performed on the RCA with the deployment of three stents. First, one stent was implanted into the proximal RCA and two stents were implanted at the level of crux of RCA with inverted TAP stenting strategy. Full anti-ischaemic treatment including dual antiplatelet therapy was initiated.
After 48 h, repeated PCI of the first obtuse marginal (OM1) and proximal LCx were performed (Supplementary material online, Video S2 and Figure 3).
Post-PCI transthoracic echocardiography revealed preserved left ventricle systolic function with an ejection fraction of 55–60%. Mild hypokinesia of the entire inferior wall, inferior septum, and infero-lateral wall detected. We did coronary computed tomography to study the anatomy. Single coronary ostium arising from the right was confirmed. It was found to have three abnormal courses of coronary arteries. Only RCA had a normal course. LCx was found to have retro-aortic course, LAD coronary artery had pre-pulmonic course, and D1 had a sub-pulmonic (septal) course. There was no interarterial course found in this case (Figure 4).
The patient was discharged on the fourth day from admission. The post-PCI period was uneventful.
Discussion
Anomalous origin of the coronary arteries, and, in particular, SCA arising from the right aortic cusp is rare.3 In our case, an SCA, with the entire right and left coronaries originating from right sinus of Valsalva was an incidental finding at the time of cardiac catheterization for acute coronary syndrome. There was no history of any congenital or valvular heart disease. However, SCA is associated with congenital anomalies such as bicuspid aortic valve, coronary arteriovenous fistula, and transposition of the great vessels.4
Our case of an SCA originating from right sinus of Valsalva, with a single ostium that quadrifurcated into LAD, D1, LCx, and a dominant RCA highlights some of the challenges encountered during a PCI in these patients. Associated coarctation has to be ruled out and aortogram is vital in such cases. A DOT sign on left ventricular angiography may be a clue to the presence of an anomalous coronary artery.5 In our case, we did not perform left ventricular angiography due to the need for emergency PCI.
An SCA originating from the right sinus has the following distribution: (i) anterior to aorta and pulmonary artery, (ii) interarterial, (iii) interseptal, and (iv) retroaortic.6 In our case, we had all three abnormal courses except interarterial.
Volume rending three-dimensional computed tomography coronary angiogram of our case confirmed an SCA arising from the right coronary sinus giving rise to right coronary artery (RCA) normal course, LCX with retro-aortic course, the diagonal artery (D1) with subpulmonic (septal) course, and LAD with pre-pulmonic course.
Our patient does not fall in any of the types described in Lipton’s classification.7
Hence, we propose a modified version of this classification of SCA—Type IV (Rajan’s and Vladimir’s) an extremely rare presentation SCA which quadfurcated into RCA, LAD, D1, and LCx.
Abnormal coronary anatomy in SCA accounts for 15% ischaemic events. The risk of having ischaemic heart diseases in SCA is high due to8:
Acute-angle take-off
Atherosclerosis
Coronary spasm
Interarterial course with associated hypoplasia
Intramural course (at the aortic wall) with lateral compression or exercise-related narrowing
Ostial ridge
Slit-like ostium.
Conclusion
Single coronary artery arising from the right aortic cusp with quadfurcation into RCA, LAD, D1, and LCx is rare. In view of the absence of inter-arterial course in our case, the need for surgical correction was not required. For such rare type of SCA, it is always wise to activate the heart team for proper assessment and better outcome.
Lead author biography
Dr Mohammed Al Jarallah is currently the head of cardiology at Sabah al Ahmed cardiac center, Kuwait. He obtained his M.B.Bch form the faculty of medicine, Kuwait University in 1999. Then, he went to do his Internal medicine training at McGill University, Quebec, Canada from the year 2001 to 2004. During which he was certified with the American board of internal medicine in 2004 and became a fellow of the Royal College of Physicians of Canada for internal medicine in 2005. He did his cardiology fellowship at McGill University from 2004 to 2007 followed by a year of fellowship in echocardiography. He was certified with the American board of cardiovascular diseases and became a fellow of the royal college of physicians of Canada for cardiology in 2007.
Supplementary material
Supplementary material is available at European Heart Journal - Case Reports online.
Supplementary Material
Acknowledgements
The authors did not received any kind of honorarium for this article.
Slide sets: A fully edited slide set detailing this case and suitable for local presentation is available online as Supplementary data.
Consent: The author/s confirm that written consent for submission and publication of this case report including image(s) and associated text has been obtained from the patient in line with COPE guidance.
Conflict of interest: none declared.
References
- 1. Fantoni JB. Observationes anatomico medicos selectiores. Turin, Italy: Medicos Selectiores, 1699. [Google Scholar]
- 2. Roberts WC, Waller BF, Roberts CS.. Fatal atherosclerotic narrowing of the right main coronary artery: origin of the left anterior descending or left circumflex coronary artery from the right (the true “left—main equivalent”). Am Heart J 1982;104:638–641. [DOI] [PubMed] [Google Scholar]
- 3. Cheezum MK, Liberthson RR, Shah NR, Villines TC, O’Gara PT, Landzberg MJ, Blankstein R.. Anomalous aortic origin of a coronary artery from the inappropriate sinus of Valsalva. J Am Coll Cardiol 2017;69:1592–1608. [DOI] [PubMed] [Google Scholar]
- 4. Tuzcu EM, Moodie DS, Chambers JL, Keyser P, Hobbs RE.. Congenital heart diseases associated with coronary artery anomalies. Cleve Clin J Med 1990;57:147–152. [DOI] [PubMed] [Google Scholar]
- 5. Laureti JM, Singh K, Blankenship J.. Anomalous coronary arteries: a familial clustering. Clin Cardiol 2005;28:488–490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Lipton MJ, Barry WH, Obrez I, Silverman JF, Wexler L.. Isolated single coronary artery: diagnosis, angiographic classification, and clinical significance. Radiology 1979;130:39–47. [DOI] [PubMed] [Google Scholar]
- 7. Roberts WC, Shirani J.. four subtypes of anomalous origin of the left main coronary artery from the right aortic sinus (or from the right coronary artery). Am J Cardiol 1992;70:119–121. [DOI] [PubMed] [Google Scholar]
- 8. Evrengul H, Ozcan EE, Turhan H, Ozturk A.. Single coronary artery originating from the right sinus of Valsalva and hypoplastic left anterior descending artery: an extremely rare combination of congenital coronary artery anomalies. Exp Clin Cardiol 2012;17:243–244. [PMC free article] [PubMed] [Google Scholar]
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