医学
依那西普
斑秃
生物仿制药
类风湿性关节炎
强直性脊柱炎
肿瘤坏死因子α
痹症科
皮肤病科
英夫利昔单抗
银屑病
免疫系统
内科学
免疫学
作者
Pelechas Eleftherios,Paraskevi V. Voulgari,Alexandros A. Drosos
标识
DOI:10.1007/s00296-022-05129-w
摘要
Alopecia areata (AA) is a common non-scaring hair loss associated with many inflammatory and autoimmune disorders. Anti-tumor necrosis factor alpha (TNFα) therapy is used to treat many chronic inflammatory disorders and has been proven to be effective and relatively safe. However, several immune-mediated skin reactions have been described with the use of TNFα inhibitors, among them AA. In this report, we describe two patients, a 32-year-old woman with ankylosing spondylitis and a 48-year-old man with rheumatoid arthritis who were both treated with SB4 (Benepali®), an etanercept biosimilar, and developed AA, 6 and 12 months respectively after the initiation of TNFα blocker biosimilar. These, are the first two cases of AA development during TNFα inhibitors biosimilar. Thus, physicians when dealing with patients treated with these agents, should be aware of possible immune skin reactions, among them AA. To this end, a close follow-up and monitoring is mandatory.
科研通智能强力驱动
Strongly Powered by AbleSci AI