Abstract：
Spontaneous coronary artery dissection (SCAD) is an atypical cause of myocardial infarction, predominantly seen in women. Among various predisposing factors, genetic vasculopathies such as connective tissue diseases significantly contribute to SCAD. This report discusses a 36-year-old male diagnosed with vascular type Ehlers-Danlos syndrome following an anterior myocardial infarction and explores relevant literature.
摘要：
自发性冠状动脉夹层（SCAD）是心肌梗死的非典型原因，主要见于女性。在各种诱发因素中，遗传性血管病变如结缔组织疾病对SCAD有重要贡献。本报告讨论了一名36岁男性，在前壁心肌梗死后被诊断为血管型Ehlers-Danlos综合征，并探讨了相关文献。
