Common origin of all three coronary arteries from the right sinus of Valsalva – first case study accompanied by mitral valve prolapse and vein anomaly, second case study followed by successful percutaneous coronary intervention of right coronary artery stenosis

Introduction

Congenital anomalies of the coronary arteries can be divided into two broad categories: those that alter myocardial perfusion and those that do not.
In coronary anomalies not altering myocardial perfusion, the coronary arteries originate from the aorta, but their origins are in unusual positions. Although myocardial perfusion is normal, the angiographer may have trouble locating them. These anomalies occur in about 0.5% to 1.0% of adult patients undergoing coronary angiography [1, 2].
Direct visualization of the proximal coronary arteries is also feasible.
With improved technology, especially the development of annular array and transesophageal 2D echocardiographic systems, the resolution required for visualizing the coronary arteries has been improved dramatically. The ultimate resolution value for examining the coronary arteries echocardiographically has yet to be determined. Researchers have indicated the usefulness of several different techniques including 2D, Doppler, color Doppler and transesophageal echocardiography in detecting congenital anomalies of the coronary arteries [3–5]. Recently, the tests that have been described in the literature as the new “gold standard” for diagnosing coronary anomalies are magnetic resonance angiography and multislice computed tomography (MSCT) [6, 7].
Anomalous origin of the left main coronary artery originating from the right or the anterior sinus of Valsalva has been associated with myocardial ischemia, myocardial infarction and sudden death [8–11].
There are a few descriptions of coronary anomalies already available in the medical literature: a case of separate origin of the left anterior descending (LAD) artery and the anomalous origin of the circumflex artery from the right sinus of Valsalva [12–14].
The origin of the left coronary artery from the right sinus of Valsalva can be dangerous during physical activity, whereas the narrowing of the coronary arteries associated with the angle of the origin of the coronary arteries and the pressure between the aorta and the path of right ventricular outflow can lead to sudden cardiac death. We present here two cases of very rare anomalous origin of coronary arteries. The first patient with coronary abnormalities had accompanying venous anomaly of lower extremities and mitral valve prolapse as well, but no atherosclerosis present. The patient was in the follow-up program for six years. The second patient had a history of anterior wall myocardial infarction (MI) and angioplasty with stent implantation. The extraordinary passage of the left coronary artery between the pulmonary trunk and sternum, undetectable in coronarography, was discovered due to MSCT.

Case reports

First case

A 38-year-old patient was admitted to the hospital with a year long history of substernal chest pain, exacerbated by stress and lasting about 10 min. The patient also reported experiencing several syncope episodes, each lasting a few minutes, over the course of about one year. He also had an 18-year history of cigarette smoking of 20 cigarettes a day, except for the last 2 months, when he quit smoking. The patient also had a family history of coronary diseases. His brother and father had myocardial infarction at the age of 40 and 62 respectively and his mother was diagnosed with ischemic heart disease.
Physical examination revealed quiet systolic murmur in the mitral area, blood pressure (BP) 120/80 mm Hg, lungs clear by auscultation and huge superficial varicose veins of both lower extremities, especially on the left side.
Electrocardiogram showed regular sinus rhythm, approx. 62/min, significant Q wave in lead III, a low voltage R wave in aVF, a flat and inverted T wave in lead III and a flat T wave in lead aVF.
The exercise (treadmill) test with the Bruce protocol showed submaximal rhythm 157/min, achieved rhythm 160/min, and metabolic equivalent (MET) 11.5. The reason for stopping the submaximal rhythm was tiredness. Blood pressure before and after the test was respectively 95/60 mm Hg, and 130/70 mm Hg. The stress test was negative. 24-hour EKG with Holter method: heart rate (HR) 75/min; no arrhythmia or heart blocks were present.
Chest X-ray: except for small degenerative changes of cervical vertebra there were no pathological changes present.
Transthoracic echocardiography (Hewlett-Packard Sonos 2000) visualized normal size left ventricle with proper contractility both general and segmental, ejection fraction (EF) 55%, mitral valve cusps with myxomatous changes and prolapse tendency with small mitral insufficiency.
Transesophageal echocardiography in short axis view visualized the left descending artery originating from the right coronary sinus and passing between the aorta and pulmonary artery.
Perfusion scintigraphy showed no significant ischemia of the heart in exertional recording, and slight hypokinesis of the apex area in resting recording.
The MSCT of the coronary arteries was performed. It revealed a strong right coronary artery. The left anterior descending artery also originates from the right sinus of Valsalva very close to the right coronary artery (RCA). It passes in an unusual way between the pulmonary trunk and sternum. The circumflex artery has its own origin at the right sinus of Valsalva, passes between the aorta and pulmonary trunk and is very weak. The system of RCA is dominating. There was no sign of coronary heart disease (Figs. 1 A, B).
However, it was decided to perform catheterization. It confirmed the MSCT diagnosis.
X-ray contrast coronary angiography: the LAD artery originates from the right coronary sinus and passes behind the aorta reaching the mid point of the anterior-lateral segment; the circumflex (CX) artery is a small artery and has a separate place of origin from the right coronary sinus; the RCA is a very big vessel supplying both of the inferior and posterior walls as well as the apex and part of the anterior wall. Hemodynamic study showed the coronary arteries without any stenosis. All of the coronary arteries originate from the right coronary sinus with the right coronary artery dominating (Figs. 2, 3).
Selective coronary angiography of the family members was performed. Both the father (the indication for the test was a typical cardiac chest pain) suggested therapy was coronary artery bypass graft (CABG) and the brother showed no coronary anomalies.
Peripheral vascular sonography:
– Right leg: Deep venous system without thrombosis and sufficient. Both of the superficial veins – the greater saphenous vein (GSV) and long saphenous vein (LSV) – are also sufficient. The posterior saphenous auxiliary vein is dilated, 13–15 mm in diameter without thrombosis. Perforating veins are sufficient as well. Antegrade venous flows show appropriate respiratory phases.
– Left leg: The deep venous system is sufficient. The GSV show no thrombosis. There is insufficiency of the common origin with the anterior saphenous auxiliary vein. The trunk is dilated 10 mm in diameter. The anterior saphenous auxiliary vein shows no thrombosis. The anterior surface of the thigh and calf show presence of the connecting vein conglomerations, 3–9 mm in diameter, without thrombosis. The GSV is sufficient. The perforating veins of the calf on the medial, posterior and lateral surface show medium degree dilatation with 4–5 mm diameter. Conclusion: Chronic, bilateral venous insufficiency especially on the left side (Fig. 4).
Cardiosurgical consultation: Suggested follow-up examination every 6 months.
Stress test: (5 years later) submaximal rhythm 154/min, achieved rhythm 130/min, exertion 8.5 MET; the reason for stopping the test was shortness of breath.
Follow-up echocardiography (same period as above): somewhat worse general contractility, EF 50%, otherwise no changes compared to the original test.
The MSCT and X-ray coronary angiography show no atherosclerosis in coronary vessels.

Second case

A 68-year-old woman was referred to our Cardiological Department with unstable angina (positive troponin assay) after she suffered an anterior wall MI without a significant Q wave 3 weeks before. She had no history of cardiac pain until the recent MI, but she had a long history of hypertension and 3 incidents of ischemic stroke (17, 10 and 2 years ago). There was a significant family history – the patient’s sister died from sudden cardiac death at the age of 70.
The physical examination at the time of admission showed: BP 160/90 mm Hg, regular heart rate 60/min, lungs clear in auscultation, quiet systolic murmur in Erb point, bilateral varicose veins of both calves, more significant on the left side, and also obesity of medium degree with body mass index (BMI) 31 kg/m².
Additional tests revealed:
– EKG: regular sinus rhythm 60/min, left axis deviation, right bundle branch block, T waves inverted in all chest leads.
– Echocardiography: end diastolic volume of left ventricle 80 ml, without segmental contractility disturbances, thickness of interventricular septum 1.4 cm, posterior wall 1.2 cm, left atrium area 18 cm², right atrium area 16 cm², right ventricle not enlarged 2.4 cm, ascending aorta 3.5 cm in diameter, mitral valve shows minimal retrograde wave and thick, incrusted cusps, additionally the posterior mitral cusp has limited mobility without significant gradient, aortic valve shows punctuate calcifications, without gradient; the tricuspid and pulmonic valves are without organic changes.
– X-ray contrast coronary angiography revealed coronary artery anomalies with common origin of the left and right coronary arteries from the aortic bulb. The trunk showed no changes, both left descending and diagonal arteries closed, circumflex artery (CX) regression of obtuse marginal (OM), no changes, right circumflex artery greatly dominating, with critical narrowing in segment 2.
After pre-dilation of the right coronary artery with a 2.5/20 mm balloon, a 4.0/15 mm Chopin stent was implanted (Figs. 5, 6).

Discussion

Congenital anomalies of the coronary arteries are usually of three categories: (1) origin of one or more coronary arteries from abnormal position in the coronary sinus, including origin of the left main coronary artery from the right aortic sinus; (2) origin of the coronary arteries from the pulmonary artery; (3) single coronary artery from the aorta.
Anomalous origin of the left coronary artery from the pulmonary artery accompanied by mitral valve prolapse and regurgitation were found in the literature [15, 16].
A 38-year-old patient was referred to our department presenting common origin of three coronary arteries from the right sinus of Valsalva accompanied by mitral valve prolapse and vein anomalies in lower extremities.
The atypical origin and unusual passage of the coronary arteries can be asymptomatic for many years. With time the addition of atherosclerotic complications exacerbates the symptoms and complicates the clinical picture. The choice of the revascularization method is difficult. The technical difficulties increase the risk of cardiosurgical revascularization and the angioplasty as well. Stent implantation seems to be the safer method for a patient with coronary anomalies, increasing the safety and reducing the frequency of restenosis.

Disclosure

Authors report no conflict of interest.

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