Combaret Nicolas, Souteyrand Géraud, Motreff Pascal
Department of Cardiology, CHU Clermont-Ferrand, CNRS, Université Clermont Auvergne, 58 rue Montalembert, 63000 Clermont-Ferrand, France.
Eur Heart J Case Rep. 2024 Oct 26;8(11):ytae567. doi: 10.1093/ehjcr/ytae567. eCollection 2024 Nov.
Spontaneous coronary artery dissection (SCAD) remains a rare form of acute coronary syndrome (ACS) in young women. It is not always easy to diagnose and its management can be complex, particularly in the case of severe forms.
A 29-year-old Mahorese woman presented with non-ST-elevation acute coronary syndrome 72 h after vaginal delivery of an uncomplicated twin pregnancy. Coronary angiography revealed a SCAD of the left anterior descending artery (LAD) treated medically. At Day 4, urgent coronary angiography was performed due to recurrent ACS with unfavourable evolution on LAD SCAD with worsening flow and appearance of right coronary artery (RCA) dissection. Percutaneous coronary intervention (PCI) was performed with drug-eluting stent (DES) implantation in LAD under optical coherence tomography (OCT) guidance. At Day 6, the patient suffered from inferior ST segment elevation myocardial infarction due to extension of the RCA SCAD with occlusion of the posterior descending artery. Once again, under OCT guidance, PCI was performed in RCA with implantation of four DES. At Day 8, the patient presented with an intra-hospital cardiac arrest by electromechanical dissociation. Urgent coronary angiography revealed a diffuse extension of the SCAD to the circumflex artery and the left main trunk (LM). Rescue PCI of the LM was performed under OCT guidance, and a femoro-femoral extracorporeal life support was implanted because of haemodynamic instability. With no hope of left ventricular ejection fraction recovery, the patient eventually benefited from a heart transplant 12 days after the first ACS with excellent evolution.
Although the majority of SCAD have a favourable outcome with spontaneous healing, it is important to keep in mind that certain severe forms exist and could require specific management as PCI under OCT guidance and potential transfer to surgical centres where heart transplants and mechanical circulatory support are available.
自发性冠状动脉夹层(SCAD)仍是年轻女性急性冠状动脉综合征(ACS)的一种罕见形式。其诊断并非总是容易,管理可能很复杂,尤其是在严重形式的情况下。
一名29岁的马霍雷斯族女性在顺产双胎妊娠72小时后出现非ST段抬高型急性冠状动脉综合征。冠状动脉造影显示左前降支(LAD)发生SCAD,接受药物治疗。在第4天,由于复发性ACS且LAD的SCAD病情进展不利,血流恶化且右冠状动脉(RCA)出现夹层,遂进行了紧急冠状动脉造影。在光学相干断层扫描(OCT)引导下,对LAD植入药物洗脱支架(DES)进行经皮冠状动脉介入治疗(PCI)。在第6天,患者因RCA的SCAD扩展导致后降支闭塞,出现下壁ST段抬高型心肌梗死。再次在OCT引导下,对RCA植入4枚DES进行PCI。在第8天,患者在医院内发生电机械分离导致的心搏骤停。紧急冠状动脉造影显示SCAD弥漫性扩展至回旋支动脉和左主干(LM)。在OCT引导下对LM进行了抢救性PCI,由于血流动力学不稳定,植入了股-股体外膜肺氧合。由于左心室射血分数无望恢复,患者最终在首次ACS发作12天后接受了心脏移植,病情进展良好。
尽管大多数SCAD可自发愈合,预后良好,但必须牢记存在某些严重形式,可能需要特殊管理,如在OCT引导下进行PCI,并可能转至具备心脏移植和机械循环支持的外科中心。