Al Emam Abdel Rahman A, Almomani Ahmed, Gilani Syed A
Department of Internal Medicine, University Of Texas Medical Branch, Galveston, Texas.
Division of Cardiology, University Of Texas Medical Branch, Galveston, Texas.
Int J Angiol. 2014 Dec;23(4):275-80. doi: 10.1055/s-0033-1349163.
Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome. It occurs predominantly among younger females and typically in the absence of atherosclerotic coronary artery disease. It is associated with peripartum period, connective tissue disorders, vasculitides, and extreme exertion. Presentations vary greatly, and this condition can be fatal. Given its rarity, there are no guidelines for management of SCAD. We present the cases of two female patients, with no coronary artery disease risk factors or recent pregnancy, who were presented with non-ST elevation myocardial infarction (NSTEMI) and ST elevation myocardial infarction (STEMI), respectively, secondary to SCAD. Both had excellent outcome after emergent percutaneous intervention. Our first patient was presented with NSTEMI with ongoing chest pain and dynamic electrocardiogram (ECG). Emergent left heart catheterization was significant for first obtuse marginal (OM1) dissection, confirmed by optical coherence tomography. Percutaneous coronary intervention (PCI) with two bare metal stents was performed with resolution of symptoms and ECG changes. The second patient is known to have syndrome, presented with STEMI and emergent coronary angiography showed left anterior descending dissection with intramural hematoma confirmed by intravascular ultrasound and treated with a drug-eluting stent with resolution of symptoms and ST changes. Her hospital course was complicated by post-myocardial infarction pericarditis that was improved with colchicine. Both the patients were observed in the coronary care unit for 24 hours. Both remained asymptomatic at 6-month follow-up. SCAD is a rare cause of acute coronary syndrome. In patients with early presentation, limited disease, and ongoing symptoms, emergent cardiac catheterization with percutaneous intervention has excellent outcome. More studies are needed to establish evidence-based management guidelines.
自发性冠状动脉夹层(SCAD)是急性冠状动脉综合征的一种罕见病因。它主要发生在年轻女性中,通常不存在动脉粥样硬化性冠状动脉疾病。它与围产期、结缔组织疾病、血管炎和过度劳累有关。临床表现差异很大,这种情况可能是致命的。鉴于其罕见性,目前尚无SCAD的管理指南。我们报告了两名女性患者的病例,她们均无冠状动脉疾病危险因素或近期妊娠史,分别因SCAD继发非ST段抬高型心肌梗死(NSTEMI)和ST段抬高型心肌梗死(STEMI)。两人在紧急经皮介入治疗后均取得了良好的效果。我们的首例患者表现为NSTEMI,伴有持续胸痛和动态心电图(ECG)变化。紧急左心导管检查显示第一钝缘支(OM1)夹层,光学相干断层扫描证实。采用两枚裸金属支架进行经皮冠状动脉介入治疗(PCI),症状和ECG变化均得到缓解。第二名患者患有综合征,表现为STEMI,紧急冠状动脉造影显示左前降支夹层并伴有壁内血肿,血管内超声证实,采用药物洗脱支架治疗后症状和ST段变化均得到缓解。她的住院过程因心肌梗死后心包炎而复杂化,秋水仙碱治疗后病情好转。两名患者均在冠心病监护病房观察24小时。6个月随访时两人均无症状。SCAD是急性冠状动脉综合征的罕见病因。对于早期表现、病变局限且症状持续的患者,紧急心脏导管检查并进行经皮介入治疗可取得良好效果。需要更多研究来制定基于证据的管理指南。