Coronary Artery Ectasia-A Review of Current Literature

Subodh Devabhaktuni, Ana Mercedes, Jimmy Diep, Chowdhury Ahsan, Subodh Devabhaktuni, Ana Mercedes, Jimmy Diep, Chowdhury Ahsan

Abstract

Coronary artery ectasia (CAE) is one of the uncommon cardiovascular disorders. Its incidence ranges from 1.2%-4.9%. Coronary artery ectasia likely represents an exaggerated form of expansive vascular remodeling (i.e. excessive expansive remodeling) in response to atherosclerotic plaque growth with atherosclerosis being the most common cause. Although, it has been described more than five decades ago, its management is still debated. We therefore reviewed the literature until date by searching PubMed and Google scholar using key words "coronary artery ectasia", "coronary artery aneurysm", "pathophysiology", "diagnosis", "management" either by itself or in combination. We reviewed the full articles and review articles and focused mainly on pathophysiology, diagnosis and management of CAE.

Figures

Fig. (1)
Fig. (1)
Coronary angiogram showing ectasia of the left main coronary artery, left anterior descending artery, ramus intermedius, proximal left circumflex (a) and right coronary artery (b).
Fig. (2)
Fig. (2)
Pathogenesis of coronary artery ectasia. RAS-Renin Angiotensin system. A number of factors implicated in the atherosclerotic process promote the expression and activity of matrix degrading enzymes, which cause severe disruption in the internal elastic lamina (IEL) and provide a gateway for the inflammatory cells to extend into the media, favoring excessive expansive remodeling and ultimately leading to formation of coronary ectasia. Adapted with permission from A.P. Antoniadis et al. [6].
Fig. (3)
Fig. (3)
Histology of the left circumflex coronary artery aneurysm. A. Tunica intima expanded by atherosclerosis (left) and tunica media attenuated and densely infiltrated by inflammatory cells (right) (hematoxylin-eosin, original magnification x10). B. Higher power showing the inflammatory cells to be predominantly lymphocytes, with a few residual smooth muscle cells (bottom center) (hematoxylin-eosin, original magnification x20). Reproduced with permission from Nichols et al. [16].

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Source: PubMed

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