PDF(Pubmed)
Abstract：
Systemic lupus erythematosus (SLE) is an autoimmune disease that can involve multiple organ systems. The most common form of vasculitis seen in SLE is small vessel vasculitis. Aortitis in SLE or antiphospholipid syndrome is an extremely rare complication. Here, we present a 32-year-old female who presented with a history of prolonged abdominal pain, who was evaluated and diagnosed to have aortitis as an unusual involvement in SLE with secondary antiphospholipid antibody syndrome.
摘要：
系统性红斑狼疮（SLE）是一种自身免疫性疾病，可累及多个器官系统。SLE中最常见的血管炎形式是小血管血管炎。SLE或抗磷脂综合征的主动脉炎是极其罕见的并发症。这里,我们介绍了一位32岁的女性，她有长期腹痛的病史，他被评估并诊断为主动脉炎，因为SLE伴继发性抗磷脂抗体综合征的异常受累。
