Fig 1: Ruptured giant right coronary artery aneurysm (white arrow).
Ninety percent of these aneurysms are of atherosclerotic origin, often occurring in relation to other atheromas in the coronary arterial tree and often associated with post-stenotic dilatation and ectasia.[6] Kawasaki disease is another important cause, which occurs usually in infants and children but where coronary artery aneurysms may be discovered much later in adulthood.[7] Other causes include polyarteritis nodosa, Marfan syndrome, syphilis, trauma, and congenital causes.[8] In our case, we have described there was evidence of mild atherosclerotic heart diseases. Although histological evaluation also suggested of the mass showed a mild atherosclerotic RCA aneurysm wall with thrombus within it. There was no evidence childhood history of Kawasaki disease, nor was there any evidence of an acute inflammatory disease or other acquired causes. Because of this, in the current report, we have described a case of ruptured atherosclerotic aneurysm of the RCA.
In frequency coronary aneurysms usually contain thrombus and hematoma that can cause them to present as an intramyocardial mass or, more rarely, to rupture such as in our case.[9] The inferior wall myocardial infarction was thought to have been the result of distal embolization of thrombus from the aneurysm.
With larger coronary artery aneurysms, surgical therapy may be necessary and entails excision of the aneurysm, restoration of blood flow with bypass and repair by patches or direct suture of any rupture into the ventricular or atrial chambers.[9] Surgical treatment should be recommended to coronary artery aneurysm and saphenous vein was a good selection for bypass graft when the diameter of native artery was relatively large.[10] In this case, the aneurysm was excised and the distal coronary artery was reconstructed with a saphenous vein bypass.
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