Introduction
The right coronary artery (RCA) is a branch of the ascending aorta and arises from the right aortic sinus. It lies in relation to the atrioventricular groove (AVG) submerged in the adipose tissue of the epicardium. It continues towards the posterior interventricular groove and often crosses the crux of the heart. In most of the subjects, the RCA supplies the SA node, AV node, right atrium, most part of right ventricle excluding the part along the anterior interventricular groove and the postero-inferior part of interventricular septum.[1]
Coronary artery disease (CAD) is the single most common cause of death in the developed world. CAD accounts for 1 of every 5 deaths given the unhealthy food habits, sedentary lifestyle etc. On an average, the frequency of critical narrowing of RCA amounts to 30 to 40 %. Hence it becomes important to understand the variations associated with RCA. We report here one such case.
Case Report
The heart of an adult male cadaver (aged about 55 years) was being dissected for the undergraduate medical students. While dissecting the right side of the heart, a small projection was seen to rise above the surface of the heart at the upper part of the border (along the right AVG) of right ventricle. Upon dissection of the right AVG, it was found unoccupied. On further probing, atrial branches bearing a proximal origin were spotted, but no ventricular branches were seen. Exposure of the upper part of the right AVG revealed the presence of the RCA (Fig 1a). Its first branch (ventricular) was atypically looped bearing two bends and passed towards the myocardium of the right ventricle (Fig 1b). The space underneath the loop was filled with adipose tissue. It then went astray in the myocardium of the right ventricle.
RCA further gave rise to many long atrial branches of very thin caliber which coursed across the AVG and went in to right atrium (Fig 1b). Few atrial branches coursed along the right AVG before entering the right atrium. The main trunk then entered the myocardium of the right ventricle. The ventricular branches initially coursed superficially in the right ventricular wall and then passed on to deeper parts. One major branch in particular (muzzled branch) travelled within the myocardium of right ventricle parallel to the right AVG, with the elevation it produced being seen on the surface. It then emerged on to the surface of the heart and continued as the right marginal artery.
For the further part, the RCA was not seen in the AVG (Fig 2) and it did not reach the crux of the heart. The coronary sinus was the sole relation to the AVG.
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Figure 1: Dissection of right coronary artery (RCA) in an isolated heart specimen (a) and closer view of its looped and muzzled branches (b). The muzzled branch is continuing as right marginal artery. SVC : Superior vena cava , AVG- Atrioventricular groove.
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Figure 2: Posterior view of the heart showing absence of right coronary artery (RCA) from atrioventricular groove (AVG) |
Discussion
Number of scientific literatures evidenced the variations in the origin of coronary arterial system of the heart. But, the unusual morphology of their branches are quite rare. Yamanaka and Hobbs in 1990 mentioned that coronary artery anomalies (CAA) are incidentally discovered during coronary angiographic study or while performing an autopsy with incidence rate of 0.64% to 1.3%.[2] In the case we report here, we discovered the variation during cadaveric dissection. Lluri et al [3] classify coronary artery anomalies in to 2 main categories. And both categories pertain to origin of the coronary artery. One category contains those originating from the opposite aortic sinus and the other includes those originating from the pulmonary trunk. Absence of RCA has been reported by few authors.[4,5] Studies on variant origin of RCA have been conducted. Elliott et al [6] and Ayalp et al [7] in their studies involving vast number of subjects enumerate the variant origins of RCA. Papadopaolos et al [8] discuss about the agenesis of the RCA ostium. In the present case, origin of RCA was normal but the variations were seen in its course and some of its branches.
In the literature review, a looped course of the RCA is reported by Satija et al.[9] In their reported case, the RCA was found to loop around the pulmonary trunk. The looping seen in the present case was not near the pulmonary trunk. The passage of the ventricular branches within the myocardium may give the appearance of a myocardial bridge. Angelini et al in their work in 1999, discuss the consequences of the severity of myocardial bridge and conclude that in most cases they are a usual variants.[10]
Olivey et al [11] and Lluri et al [3] elaborate on the embryological basis for such variations of RCA. Olivey et all propose that an elaborate interaction of epicardial cells with myocardial cells leads to the transformation of epicardial cells into mesenchymal cells, as precursors of building blocks of coronary vessels.[11] Lluri et al [3] add on that maturation of developing coronary vessels which includes migration of smooth-muscle cells, proper arrangement of these cells, growth of some vessels, and regression of others through apoptosis. Any abnormalities during this delicate, well controlled process may lead to congenital coronary artery anomalies.
Taylor et al [12] postulate that in an anomalous course of right coronary artery in the sulcus between the pulmonary trunk and the aorta there is an increased risk of malignant arrhythmias and sudden death. In the reported case the presence of the looping above the surface of the heart may also pose similar increased risks. As said by Lluri et al [3] discrepancies in reporting suggests that not all myocardial bridges cause symptoms and symptoms if present usually act secondary to ischemia. Eckart et al in their 25-year review of autopsies in military recruits mention that cardiac abnormality accounted for 51% of sudden deaths in young adults, with coronary artery abnormality accounting for 61% of it.[13] These reports provide substantial proof that knowledge of coronary artery variations and abnormalities are highly important and not to be ignored. Angelini et al propose that choice of treatment for such CAA as supported by most of literature is surgical revascularization.[10] Coronary angioplasty with stent deployment may be employed here provided normal anatomy of the concerned coronary artery.
Conclusion
In this case, the branches of RCA present a unique loop and appears to have gone astray and are muzzled in the myocardium of the right ventricle. The course of the RCA was also incomplete and atypical as compared to its normal anatomy. Such a variation in the course of RCA accompanied by the unique looping and muzzling pattern is rare. It may pose a tough challenge to the radiologists and cardiologists in performing various procedures such as coronary stenting involving the RCA.
References
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- Yamanaka O, Hobbs RE, Coronary Artery Anomalies in 126,595 Patients Undergoing Coronary Arteriography. Cathet Cardiovasc Diagn. 1990;21(1):28-40.
- Lluri G, Aboulhosn J., Coronary Arterial Development: A Review of Normal And Congenitally Anomalous Patterns. Clin Cardiol. 2014;37(2):126-30.
- Roba S. Alhasan, Osama Qaqi, MD, Mahir D. Elder, MD. An Absent Right Coronary Artery Anomaly. In: Cath Lab Digest 2012;20(12):46-48.
- Blaschke F, Zimmermann E, Greupner J, Zohlnhoefer D, Krackhardt F, Haverkamp W, et al. A Rare Case of a Congenital Single Coronary Artery: Right Coronary Artery Originating From the Distal Left Circumflex Artery. Vascular Disease Management 2013;10(11):E244-E247.
- Elliott GE, Martin AH. Congenital absence of the right coronary artery with a unique origin of the artery to the sinu-atrial node: A case study. IJAV 2012;5:120–125.
- Ayalp R, Mavi A, Serçelik A, Batyraliev T, Gümüsburun E. Frequency in the anomalous origin of the right coronary artery with angiography in a Turkish population. Int J Cardiol. 2002;82(3):253-7.
- Papadopoulos DP, Moyssakis I, Athanasiou A, Anagostopoulou S, Benos I, Votteas VE.Right Coronary Ostium Agenesis With Absence of The Right Coronary Artery: A Rare Case Of Non-ST Elevation Coronary Syndrome, Clin Anat. 2006;19(4):345-6.
- Satija B, Sanyal K, Katyayini K. Malignant Anomalous Right Coronary Artery Detected By Multidetector Row Computed Tomography Coronary Angiography, J Cardiovasc Dis Res. 2012;3(1): 40–42.
- Angelini P, Villason S, Albert V Chan, Jose G Diez. Coronary Artery Anomalies: A Comprehensive Approach, edited by P. Angelini (chapter 4). Lippincott Williams & Wilkins, Philadelphia O 1999; pp 27-63
- Olivey HE, Svensson EC. Epicardial-myocardial signaling directing coronary vasculogenesis. Circ Res 2010;106:818–832.
- Taylor AJ, Rogan KM, Virmani R. Sudden Cardiac Death Associated With Isolated Congenital Coronary Artery Anomalies. J Am Coll Cardiol. 1992;20:640–647.
- Eckart RE, Scoville SL, Campbell CL. Sudden Death In Young Adults: A 25-year Review Of Autopsies In Military Recruits. Ann Intern Med. 2004;141:829–34.
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