An unruptured, thrombosed 10 cm right coronary artery aneurysm mimicking a pericardial cyst
© Chauhan et al.; licensee BioMed Central Ltd. 2013
Received: 14 March 2012
Accepted: 3 November 2012
Published: 7 January 2013
Giant coronary artery aneurysms are a rare and potentially life-threatening condition. A 47 year old male presented with a progressive 6 month history of dyspnea and acute right sided chest pain. During the patients work-up, a 10 cm × 10 cm right coronary artery aneurysm was discovered on CT scan and confirmed by cardiac catheterization. The patient was emergently taken to the operating room for aneurysmal resection with placement of a greater saphenous vein bypass graft. There were no post-operative complications and the etiology of this patient’s aneurysm was determined to be a congenital ectatic dilation of his right coronary artery. The patient is doing well at 2 years of clinical follow-up.
KeywordsGiant coronary artery aneurysm Right coronary artery Coronary artery bypass graft CABG
Giant coronary artery aneurysm’s are a very rare and life-threatening cardiovascular condition. The presentation of a giant coronary artery aneurysm can resemble an acute coronary syndrome with thrombosis of the aneurysmal sac and subsequent ischemic symptoms from compromised blood flow. However other serious complications such as rupture of the sac and direct compressive effects within the thoracic cavity can also cause serious morbidity and even be fatal for some patients. Therefore immediate diagnosis and cardiothoracic surgical intervention is important in decreasing morbidity and mortality for these patients.
A 47 year old male presented to the Emergency Department (ED) with right sided pleuritic chest pain for six hours. Several years prior to his presentation, he had sustained a fall from approximately 3 meters, with minor posterior chest wall trauma. The patient’s past medical and social history were unremarkable and he took no medications. On review of systems, the patient reported an increasing level of fatigue and exertional dyspnea over the past seven months. On exam, the patient’s vital signs were stable and cardiac auscultation revealed a pericardial friction rub with no murmurs or gallops. Electrocardiogram (ECG) showed an incomplete right bundle branch block with non-specific T wave changes. The cardiac enzymes revealed a slightly elevated Troponin-I level of 0.10 ng/mL.
Coronary artery aneurysm’s (CAA) are localized dilations of the artery that exceed the diameter by 1.5 times the largest adjacent normal vessel or a 50% increase in the arterial diameter compared with an adjacent arterial segment . Giant CAA’s are furthermore defined as a general vessel dilation of 2 cm or greater in diameter . A giant CAA is very rare with a reported incidence in a cardiac surgical population of 0.02%, with right coronary arteries affected greater than left [2, 3]. The common etiologies behind CAA’s are atherosclerosis, trauma, congenital malformations, infection, vasculitic diseases, and stent placement [1, 4]. Giant coronary aneurysms are more likely to be congenital as opposed to smaller coronary artery aneurysms in which the significant majority are atherosclerotic or vasculitic (e.g. Kawasaki’s disease) by origin . If not identified early or managed appropriately, complications such as thrombosis of the vessel with resultant myocardial ischemia, aneurysmal rupture with acute pericardial tamponade, or direct compressive effects from the mass lesion resembling an obstructive cardiomyopathy can occur [5, 6].
The histopathology of the aneurysm in our patient showed only chronic perivascular adventitial inflammation and revealed no distinct etiology such as infection or atherosclerosis as the cause. We also considered the traumatic accident the patient suffered seven years prior to be an unlikely cause, since the reported trauma was relatively mild and posteriorly directed, as well no prior evidence found on CT of previous sternal or rib fractures. Our examination, history, and pathologic analysis suggest that this was more likely a congenital ectatic dilatation of his RCA which had progressed over many years. Although his presenting symptoms resembled an acute coronary syndrome due to the thrombosis of the giant aneurysm, his 2-month history of prodromal symptoms was likely due to the chronic compression of his right sided cardiac chambers by the lesion.
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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