Department of Dermatology, Osaka University Graduate School of Medicine, Osaka, Japan.
Mod Rheumatol. 2012 Nov;22(6):928-30. doi: 10.1007/s10165-012-0604-2. Epub 2012 Feb 5.
Hereditary angioedema (HAE) is a life-threatening disorder caused by deficiency or dysfunction of the C1 inhibitor protein. Patients with HAE are restricted in various medical treatments, which can induce an HAE attack. We herein report the first case of psoriatic arthritis (PSA) with type 1 HAE successfully treated with 25 mg of etanercept without HAE attack. Etanercept may represent a useful choice for treating patients with HAE accompanied by intractable PSA and rheumatoid arthritis (RA).
遗传性血管性水肿(HAE)是一种由 C1 抑制剂蛋白缺乏或功能障碍引起的危及生命的疾病。HAE 患者受到多种医疗治疗的限制,这些治疗可能会引发 HAE 发作。我们在此报告首例成功接受 25 毫克依那西普治疗的 1 型 HAE 伴发银屑病关节炎(PSA)病例,且未发生 HAE 发作。依那西普可能是治疗伴发难治性 PSA 和类风湿关节炎(RA)的 HAE 患者的一种有用选择。