International Journal of the Cardiovascular Academy

CASE REPORT
Year
: 2020  |  Volume : 6  |  Issue : 2  |  Page : 86--88

Coronary artery bypass graft surgery in a rare case of coronary artery anomaly – Single coronary artery originating from the right aortic sinus


Anshuman Darbari1, Devender Singh2, Anish Gupta1, Barun Kumar3,  
1 Department of CTVS, AIIMS, Rishikesh, Uttarakhand, India
2 Department of CTVS, Kovai Medical Center and Hospital, Coimbatore, Tamil Nadu, India
3 Department of Cardiology, AIIMS, Rishikesh, Uttarakhand, India

Correspondence Address:
Dr. Anshuman Darbari
Department of CTVS, AIIMS, Rishikesh - 249 203, Uttarakhand
India

Abstract

Single coronary artery (SCA) is a very rare congenital anomaly, in which the entire coronary system arises from the solitary ostium with the incidence of 0.024%–0.066% in the general population undergoing coronary angiography. It is usually considered a benign entity but may cause chest pain, hemodynamic abnormalities, myocardial ischemia, or sudden cardiac death owing to its course arising between the pulmonary artery and aorta. The diagnosis of congenital coronary artery anomalies is usually made by conventional coronary angiography and very few cases have been reported in the literature. To the best of our knowledge, we report this as a first case, in which successful off-pump coronary artery bypass grafting was done for a SCA system.



How to cite this article:
Darbari A, Singh D, Gupta A, Kumar B. Coronary artery bypass graft surgery in a rare case of coronary artery anomaly – Single coronary artery originating from the right aortic sinus.Int J Cardiovasc Acad 2020;6:86-88


How to cite this URL:
Darbari A, Singh D, Gupta A, Kumar B. Coronary artery bypass graft surgery in a rare case of coronary artery anomaly – Single coronary artery originating from the right aortic sinus. Int J Cardiovasc Acad [serial online] 2020 [cited 2020 Oct 27 ];6:86-88
Available from: https://www.ijcva.com/text.asp?2020/6/2/86/286454


Full Text



 Introduction



Congenital coronary anomalies are found in 0.2%-1.3% of patients undergoing coronary angiography and they are further defined as any unusual pattern in origin, course or termination. In these anomalies, subset of single coronary artery (SCA) is found in approximately 0.066% of the population. This anomaly has been reported in association with and without atherosclerotic changes or in association with other congenital pathologies. Coronary arterial anomalies vary widely in clinical significance and presentations, so treatment and management is still not standardized.

 Case Report



A 63-year-old male patient presented to the cardiology department with chief complaints of left-sided chest pain off and on exertion suggestive of angina for 1½ years without any dyspnea. He was a chronic smoker and occasional alcoholic for 5 years. During the initial evaluation and workup at our hospital, his electrocardiograph was unremarkable and echocardiography was suggestive of normal left ventricular function with no regional wall motion abnormality. The physical examination and laboratory data were normal. His conventional coronary angiography (CAG) was done because of the persistent history of chest pain. We found that the entire coronary system as a common trunk arose from the single ostium and suggested an anomalous origin of the left main stem from the right Ostia, with very long main crossing the right ventricular outflow tract, left anterior descending (LAD) arose from the left main stem, and had moderate-to-severe disease in the proximal LAD artery. The left circumflex artery also arose from the left main stem and had moderate-to-severe disease in the proximal artery [Figure 1]. The right coronary artery (RCA) had severe disease from the mid vessels to the distal vessels. He was posted for off-pump coronary artery bypass grafting. After opening pericardium, purse-string sutures were taken on the aorta and right atrium appendage for possible need of cardiopulmonary bypass in case of hemodynamic instability. Operative findings were suggestive of healthy LAD, but obtuse marginal (OM) OM-1, OM-2, and posterior descending artery (PDA) were diffusely diseased [Figure 2]. Off-pump on beating heart left internal mammary artery (LIMA) to LAD grafting was done under controlled local suction stabilization of the myocardium. After it, reverse saphenous vein grafts to the PDA, OM-1, and OM-2 on the distal side and proximally to the aorta were done [Figure 3]. Intraoperatively, no hemodynamic event occurred. Postoperative recovery was smooth, and the patient was discharged after 8 days of uneventful hospital stay.{Figure 1}{Figure 2}{Figure 3}

 Discussion



In a large series of 126,595 patients undergoing CAG, a single coronary artery (SCA) from the right sinus of Valsalva was found in 0.019%. About 40% of SCA anomaly cases are associated with congenital heart diseases such as Fallot tetralogy, transposition of great arteries, persistent truncus arteriosus, and pulmonary atresia.

Initially, the classification of SCA is made by Lipton. Later, modified Lipton classification included features such as the anatomical distribution, the ostial location, and the course of the transverse trunk. Ogden in 1970 classified “SCA” into 14 basic distribution patterns. Later, Shirani and Roberts classified a SCA into 20 categories based on the location of the solitary coronary ostium and the presence or absence of an aberrant coronary artery and the course taken by the aberrant-coursing coronary artery.

In this type of SCA, the entire coronary tree arises as a common trunk from the right coronary sinus dividing into the RCA, which has a normal course and the left main coronary artery (LMCA). Then, the LMCA crosses the base of the heart turning anteriorly the aorta and dividing it into LAD and circumflex arteries. In the malignant or interarterial type of this anomaly when LMCA crosses between the aorta and pulmonary artery, patients might present with sudden death due to the compression and kinking of LMCA, especially during physical exertion. The SCA anomaly is usually asymptomatic but may present as myocardial ischemia, syncope, or sudden cardiac death (SCD) depending on its course and the presence and severity of atherosclerosis. Myocardial ischemia or SCD is usually associated with its course between the aorta and the main pulmonary artery or posterior variant.[1] Yet, there is not an established treatment strategy guide for a SCA. The course of these anomalous coronary arteries and association with atherosclerotic disease determine the treatment strategy.[2]

Terminology

In 2005, Rigatelli et al. based his classification on clinical significance of the anomaly and launched a global practical classification of four categories (Class A: benign; Class B: relevant due to fixed myocardial ischemia; Class C: severe, involved in SCD; and Class D: critical due to worsened clinical picture).[3] Due to the risk of sudden death in patients whose anomalous coronary artery courses between the aorta and pulmonary artery, coronary artery bypass surgery is useful even if patients have not severe atherosclerotic coronary stenosis. Symptomatic carriers have three treatment options: medical treatment/observation, coronary angioplasty with stent deployment, and surgical repair. Despite the limitations of our current knowledge of such anomalies, intervention may be justified in selected cases to prevent sudden death and improve the quality of life.[4],[5] Surgical strategy involves the replacement of the anomalous coronary artery to the coronary sinus appropriately or bypass surgery as in our case.

 Conclusion



The determination of the anomalous origin of the coronary artery is of great clinical importance due to its severe life-threatening complications. The new imaging modalities such as multislice computed tomography and cardiovascular magnetic resonance imaging have also emerged to enable the accurate visualization of the anatomical configurations and the detection of this structural malformation. Both these tests in addition of conventional CAG have the additional advantage of three-dimensional reconstruction of the areas of the coronaries relative to the aorta and pulmonary artery and a definitive diagnosis of squeezed aberrant coronary arteries between these great vessels. Most of the structural cardiovascular abnormalities are incidentally detected and may be symptomatic; however, a few are potentially significant and can trigger sudden death also.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

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3Rigatelli G, Rigatelli G. Congenital coronary artery anomalies in the adult: A new practical viewpoint. Clin Cardiol 2005;28:61-5.
4Said SA, de Voogt WG, Bulut S, Han J, Polak P, Nijhuis RL, et al. Coronary artery disease in congenital single coronary artery in adults: A Dutch case series. World J Cardiol 2014;6:196-204.
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