Single Coronary Artery Anomaly: A Case Report and Review of Literature

Single coronary artery (SCA) is a rare congenital anomaly where only one coronary artery arises from a single coronary ostium to supply the entire heart [1, 2]. It is usually associated with other cardiac abnormalities. SCA has variable presentation, ranging from mild non-specific symptoms up to sudden cardiac death [1].

A 56-year-old woman presented to our hospital with unstable angina. The patient complained of progressive substernal chest pain on exertion that started a few months prior to presentation, and then progressed to become more frequent and at rest. She also had associated palpitations and dizziness. Her past medical history was significant for hypertension and hyperlipidemia. On admission, vital signs showed a heart rate of 80 bpm, blood pressure of 130/90 mmHg, and temperature of 36.6 °C. Physical examination was otherwise unremarkable. Electrocardiogram showed normal sinus rhythm, with non-specific T-wave changes. Trans-thoracic echocardiogram showed normal left ventricular function and no segmental wall-motion abnormalities. Blood work showed negative cardiac troponin as well as normal complete blood count and metabolic profile.

We decided to proceed with a coronary angiogram given her clinical presentation with unstable angina. Selective coronary angiography (Fig. 1a) showed a normal left main coronary artery arising from the left coronary cusp, branching to a normal left anterior descending artery (LAD) and to a left circumflex artery (LCX). The latter was a large vessel that also supplied the territory of the right coronary artery (RCA) through its terminal extension. All vessels were free of atherosclerosis and had normal flow. Aortography (Fig. 1b) showed absence of RCA with no other vessels arising from right or non-coronary cusps. The patient was managed conservatively with emphasis on aggressive control of risk factors. Informed consent was obtained from the patient for reporting this rare case.

We report a rare case of isolated SCA with absent RCA, with LCX supplying the territory of the RCA. SCA is a congenital anatomic abnormality in which only one coronary artery originates from a single coronary ostium in the aortic sinus. It has an incidence ranging from 0.024 to 1% per various reports [1, 3, 4]. Congenital cardiac structural deformities associated with SCA include pulmonary artery atresia, tetralogy of Fallot, and patent truncus arteriosus [2]. Incidence of RCA arising from the left coronary vasculature ranges from 0.1 to 0.9% [5, 6], with most of the published cases reporting RCA originating from the proximal or middle portion of the LAD.

Lipton et al. [7] originally proposed the angiographic classification of SCA, which was later modified by Yamanaka et al. (Table 1) [4]. This classification takes into account the origin of the ostium from the sinus of Valsalva, anatomical course of the vessel, and the course of the transverse trunk. Alphabets R or L are used to identify the ostial origin of the vessel, roman numerals I, II, or III are used to represent the anatomical distribution of the vessel, and letters A, B, P, S, and C are used to delineate the course of the vessel with respect to the pulmonary artery and the aorta [4]. Per this system, our patient would be classified as LIA.

Most patients are asymptomatic at the time of diagnosis, and cases of SCA are usually found incidentally on coronary angiography. Many patients might have atypical chest pain or non-specific symptoms, with absence of obstructive coronary artery disease and negative workup for ischemia [8]. Others may present with features of typical chest pain, sudden death especially during exercise, syncope, palpitations, ventricular tachycardia, and myocardial infarction [8]. Certain anomaly classifications usually have a benign clinical course, such as RI, LI types. Meanwhile, the aberrant coronary artery courses between the outflow tracts such as R/LIIB or RIII, which makes them more prone to serious clinical complications [9]. The underlying pathophysiology could be related to the dilatation of the great outflow tracts during exercise, with secondary compression of the aberrant coronary artery along their varied course [9]. Other features, like acute take-off angle of the anomalous vessel, slit-like orifice, and proximal intramural course, are characteristics that can predispose to anginal symptoms and sudden death during exertion [5, 8].

Basso et al. [10] identified 27 cases of sudden cardiac death in young adults with congenital coronary anomalies in a retrospective review. It was observed that the patients with coronary arteries originating from contralateral sinuses were more likely to die during exertional activity. This is theorized to be secondary to compression of the anomalous vessel between the aorta and the pulmonary artery during exercise because of the dilation of the latter two vessels [11, 12]. Taylor et al. [5] looked at the records of 242 deceased patients with isolated congenital coronary anomalies and found that one-third of the patients suffered sudden cardiac death, and half of these were exercise-related deaths. Patients younger than 30 years of age were significantly more likely to suffer from sudden cardiac death compared to older patients. Younger patients were also more likely to die suddenly during physical exertion.

Coronary angiography remains the gold standard for diagnosis and classification. Echocardiography is useful mainly to delineate other structural abnormalities accompanying the SCA. Computed tomography angiography offers a less-invasive imaging modality despite requiring administration of contrast media. Cardiovascular magnetic resonance (CMR) is a suitable alternative investigation for assessing coronary anatomy. Advantages extended by CMR include lack of exposure to ionizing radiations, no need to use iodinated or ionized intravenous contrast media, no restrictions imposed by body habitus, simultaneous evaluation of multiple parameters of cardiovascular anatomy, perfusion and function, along with the ability to achieve high spatial and temporal resolutions to better assess structural abnormalities [13].

Treatment options include conservative medical management, percutaneous coronary intervention (PCI) with stent placement, and surgical correction. Most asymptomatic patients do not require invasive therapy and should be managed with strict control of risk factors. Given the variety of anatomical presentations, a multidisciplinary approach involving cardiothoracic surgery and interventional cardiology can be considered to determine the best course of action in symptomatic patients. Presentations with unstable angina, similar to our case, have been previously described in cases of SCA. While some of those patients improved with medical treatment, others had obstructive coronary disease requiring intervention.

PCI in cases of SCA poses certain technical challenges. The abnormal origin and course in cases of SCA lead to difficulties in cannulation of the coronary ostium as well as difficulties in providing optimal catheter support during PCI [14]. Awareness of those variations is important for catheter-based treatment. Rudan et al. [13] successfully performed PCI with stent placement in a case of SCA where RCA originated as extension of left coronary vasculature. Kafkas et al. [15] reported successful stent placement in an L1 type SCA. Other case reports also demonstrated successful management of similar lesions by PCI [14, 16].

Surgical options include osteoplasty, coronary artery bypass grafting (CABG) of the anomalous artery, re-implantation of the anomalous artery to the aorta, and pulmonary artery translocation [5, 17]. Rinaldi et al. [17] reported the management of eight cases of anomalous RCA plus slit ostium with ostial widening. Others reported successful management by CABG in two symptomatic patients with SCA complicated by stenotic lesions along the vessel course [18]. Pulmonary artery translocation is usually reserved for patients with coronary arteries arising from the contralateral coronary sinus without stenotic or slit-like lesions along the vessel [5].

Due to the lack of stenotic lesions, acute angle cut-off and slit-like lesions, our patient was managed medically with risk factor control.

We report a rare case of SCA, a rare congenital abnormality. Patients are usually asymptomatic, however, may present with typical chest pain, ventricular fibrillation, or myocardial infarction. Cardiologists should be aware of this rare condition, which has been associated with sudden cardiac death in young individuals. Management usually involves a multi-disciplinary approach with interventionists and surgeons aiming for an individualized plan based on presentation and anatomy of each case.