Mobilia Gianni, Donato Antonino, Micari Antonio, Micari Giovanni, Satullo Gaetano, Grassi Rosario
U.O. di Cardiologia, Azienda Ospedaliera Papardo, Messina.
Ital Heart J Suppl. 2002 Oct;3(10):1042-6.
Antiphospholipid syndrome is a thrombotic disorder in which the clinical features are venous and/or arterial thrombosis, thrombocytopenia, and recurrent fetal loss. We describe the case of a 39-year-old woman affected by antiphospholipid syndrome and acute anterior myocardial infarction complicated by cardiogenic shock. The patient, after the failure of thrombolysis, was successfully treated by rescue angioplasty. The persistent thrombocytopenia of these patients may lead to safety problems in thrombolytic treatment; therefore, primary angioplasty may be considered the treatment of choice.
抗磷脂综合征是一种血栓形成性疾病,其临床特征为静脉和/或动脉血栓形成、血小板减少和反复流产。我们描述了一例39岁患有抗磷脂综合征并伴有心源性休克的急性前壁心肌梗死女性患者的病例。该患者在溶栓治疗失败后,通过补救性血管成形术成功治愈。这些患者持续存在的血小板减少可能会导致溶栓治疗中的安全问题;因此,原发性血管成形术可被视为首选治疗方法。