Cardenas Gustavo A, Grines Cindy L, Sheldon Mark, Goldstein James A
Division of Cardiology, William Beaumont Hospital, Royal Oak, MI 48073, USA.
South Med J. 2008 Apr;101(4):442-6. doi: 10.1097/SMJ.0b013e318167b819.
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.
一名45岁的女性运动员,无心血管疾病史或冠状动脉危险因素,因自发性右冠状动脉夹层出现非ST段抬高型心肌梗死。她接受了药物治疗,症状得到缓解。因反复运动时胸痛进行的重复血管造影显示TIMI-3血流,且无夹层证据。血管内超声记录了血肿消散的离散区域,但无夹层瓣或管腔受压>30%的情况。6个月后的冠状动脉计算机断层扫描显示无任何血管异常。在对胸痛、心肌梗死或心源性猝死的年轻患者进行鉴别诊断时,应考虑这种罕见但可能致命的疾病,特别是如果涉及围产期妇女或使用口服避孕药的妇女,或无冠状动脉粥样硬化或传统心血管危险因素证据的患者。