Korkontzelos Ioannis, Kotsia Anna, Mpourazanis George, Natsios Angelos, Korkontzelou Pantelina-Danai, Karanikis Pavlos, Pappa Evgenia, Papalexis Petros
Department of Obstetrics and Gynecology, Ioannina State General Hospital "G. Chatzikosta", Ioannina, GRC.
Department of Cardiology, Ioannina State General Hospital "G. Chatzikosta", Ioannina, GRC.
Cureus. 2024 Apr 28;16(4):e59182. doi: 10.7759/cureus.59182. eCollection 2024 Apr.
Marfan syndrome (MFS) is a rare hereditary connective tissue disorder with autosomal dominant inheritance associated with an increased risk of cardiovascular complications due to connective tissue fragility. Acute myocardial infarction during pregnancy is also a rare event associated with poor maternal and fetal outcomes. Herein, we report a case of a 30-year-old pregnant woman with a known history of MFS. The patient had been treated surgically for an ascending aorta aneurysm and mechanical prosthetic aortic valve repair. She presented at 12 weeks of gestation with severe chest pain, which proved to be acute myocardial infarction. This is believed to be the first case of this complex medical condition presented in the first trimester of pregnancy.
马凡综合征(MFS)是一种罕见的遗传性结缔组织疾病,具有常染色体显性遗传,由于结缔组织脆弱,心血管并发症风险增加。妊娠期急性心肌梗死也是一种罕见事件,与母婴不良结局相关。在此,我们报告一例30岁有马凡综合征病史的孕妇。该患者曾接受升主动脉瘤手术治疗及机械人工主动脉瓣修复术。她在妊娠12周时出现严重胸痛,经证实为急性心肌梗死。据信这是首例在妊娠早期出现这种复杂病症的病例。