Houck Philip D, Strimel William J, Gantt D Scott, Linz Walter J
Division of Cardiology, Department of Medicine, Scott & White Healthcare, Temple, Texas 76508, USA.
Tex Heart Inst J. 2012;39(2):244-8.
Peripartum myocardial infarction is a rare event that is associated with high mortality rates. The differential diagnosis includes coronary artery dissection, coronary artery thrombosis, vascular spasm, and stenosis. Our evaluation of 2 cases over a 5-year time period has led to a hypothesis that peripartum myocardial infarction is an immune-mediated event secondary to coronary endothelial sensitization by fetal antigen. In our patients, we supplemented standard medical therapy with immunotherapy consisting of corticosteroids, plasmapheresis, and intravenous immunoglobulin. Herein, we present our most recent case-that of a 29-year-old black woman (gravida V, para IV), 2 weeks postpartum with no relevant medical history. She presented with a 1-week history of chest pain. Initial electrocardiographic and cardiac biomarkers were consistent with acute coronary syndrome. Echocardiography revealed reduced systolic function with inferior-wall hypokinesis. Angiography revealed diffuse disease with occlusion of the left anterior descending coronary artery not amenable to revascularization. We were successful in treating the myocardial infarction without the use of catheter-based interventions, by modifying the immunologic abnormalities. Two cases do not make a protocol. Yet we believe that this case and our earlier case lend credence to the hypothesis that peripartum myocardial infarction arises from sensitization by fetal antigens. This concept and the immune-modifying treatment protocol that we propose might also assist in understanding and treating other inflammatory-disease states such as peripartum cardiomyopathy and standard acute myocardial infarction. All of this warrants further investigation.
围产期心肌梗死是一种罕见事件,与高死亡率相关。鉴别诊断包括冠状动脉夹层、冠状动脉血栓形成、血管痉挛和狭窄。我们在5年时间内对2例病例的评估得出一个假设,即围产期心肌梗死是胎儿抗原导致冠状动脉内皮致敏后的免疫介导事件。在我们的患者中,我们在标准药物治疗的基础上补充了由皮质类固醇、血浆置换和静脉注射免疫球蛋白组成的免疫治疗。在此,我们介绍我们最近的病例——一名29岁的黑人女性(孕5产4),产后2周,无相关病史。她有1周的胸痛病史。初始心电图和心脏生物标志物与急性冠状动脉综合征一致。超声心动图显示收缩功能降低,下壁运动减弱。血管造影显示弥漫性病变,左前降支冠状动脉闭塞,无法进行血管重建。通过纠正免疫异常,我们成功地在未使用基于导管的干预措施的情况下治疗了心肌梗死。两例病例不能形成一个方案。然而,我们相信这个病例和我们之前的病例支持了围产期心肌梗死源于胎儿抗原致敏的假设。我们提出的这一概念和免疫调节治疗方案也可能有助于理解和治疗其他炎症性疾病状态,如围产期心肌病和标准急性心肌梗死。所有这些都值得进一步研究。