Why the study?
Spontaneous coronary artery dissection is an under-recognized cause of acute coronary syndrome, especially in middle-aged women without conventional atherosclerotic risk factors.
Case Report (n=5)
This case series highlights the varied clinical and angiographic presentations of SCAD and supports individualized management, predominantly favoring conservative therapy.
May prompt SCAD consideration in middle-aged ACS without risk factors; case series leaves open prospective validation of management.
Spontaneous coronary artery dissection is an under-recognized cause of acute coronary syndrome, especially in middle-aged women without conventional atherosclerotic risk factors. We present a series of five patients (three women, two men; mean ages 60 and 51 years, respectively) who presented with acute chest pain or progressive angina. Electrocardiographic findings ranged from ST-segment elevation to non-ST-elevation patterns. Coronary angiography demonstrated type I, type IIB or type III spontaneous coronary artery dissection according to the Saw classification, predominantly involving the mid-to-distal left anterior descending artery; one patient had concomitant mid-right coronary artery occlusion. Four patients were managed conservatively with single antiplatelet therapy, beta-blockers and blood-pressure control; one required stenting of an occluded right coronary artery. All recovered without recurrence during short-term follow-up. The series underscores the need for a high index of suspicion, careful angiographic interpretation and individualized decisions between conservative therapy and revascularization.
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I. et al. (2026) conducted a case report in Spontaneous coronary artery dissection (SCAD) (n=5). Conservative therapy or revascularization was evaluated on Recovery without recurrence.
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