Gupta Ajay, Chandra Nishith, Kler T S
Department of Cardiology, Escorts Heart Institute and Research Centre, New Delhi.
Indian Heart J. 2002 May-Jun;54(3):301-3.
A 41-year-old woman diagnosed with aortoarteritis since 1988 was admitted with unstable angina. She also had anemia, thrombocytopenia, aortic regurgitation and pulmonary artery hypertension. She gave a history of recurrent fetal loss and myocardial infarction, following which angioplasty to the left anterior descending artery had been done. After investigation, a diagnosis of aortoarteritis with systemic lupus erythematosus and associated antiphospholipid antibody syndrome was made. Aortoarteritis may coexist with systemic lupus erythematosus and associated antiphospholipid antibody syndrome.
一名自1988年起被诊断为大动脉炎的41岁女性因不稳定型心绞痛入院。她还患有贫血、血小板减少症、主动脉瓣关闭不全和肺动脉高压。她有反复流产和心肌梗死病史，之后对左前降支进行了血管成形术。经过检查，诊断为大动脉炎合并系统性红斑狼疮及相关抗磷脂抗体综合征。大动脉炎可能与系统性红斑狼疮及相关抗磷脂抗体综合征共存。
