Key result
Medical treatment of a 45-year-old female with spontaneous right coronary artery dissection resulted in resolution of symptoms and absence of vascular abnormalities on CT at 6 months.
Case Report (n=1)
Medical management of spontaneous coronary artery dissection in a young female athlete resulted in complete clinical and angiographic resolution at 6 months.
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May support conservative SCAD management in select cases; hypothesis-generating and leaves optimal strategy open pending prospective trials.
A 45-year-old female athlete with no history of cardiovascular disease or coronary risk factors presented with a non-ST-segment elevation myocardial infarction due to spontaneous right coronary artery dissection. She was treated medically with resolution of her symptoms. Repeat angiography due to recurrent exertional chest discomfort showed TIMI-3 flow and no evidence of dissection. Intravascular ultrasound documented discrete areas of resolving hematoma, but no dissection flap or impingement of the lumen >30%. A coronary computed tomography 6 months later revealed absence of any vascular abnormalities. This rare but potentially lethal condition should be considered in the differential diagnosis of young patients with chest pain, myocardial infarction, or sudden cardiac death, especially if it involves women either in the peripartum period or those using oral contraceptives, or patients without evidence of coronary atherosclerosis or traditional cardiovascular risk factors.
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Cardenas et al. (2008) conducted a case report in Spontaneous coronary artery dissection (n=1). Medical treatment was evaluated on Resolution of symptoms and vascular abnormalities. Medical treatment of a 45-year-old female with spontaneous right coronary artery dissection resulted in resolution of symptoms and absence of vascular abnormalities on CT at 6 months.
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