Stevens-Johnson syndrome in a patient with rheumatoid arthritis during long-term etanercept therapy.

Agnieszka Owczarczyk-Saczonek, Natalia Zdanowska, Aleksandra Znajewska-Pander, Waldemar Placek
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引用次数: 7

Abstract

Background: Etanercept and other anti-TNF-alpha agents have been indicated as a therapeutic option in severe drug reactions, including Stevens-Johnson syndrome and toxic epidermal necrolysis. Etanercept has been shown to quickly reduce the detachment of the epidermis and shorten healing time. Cases of etanercept-induced severe adverse drug reactions were also described.

Main observations: A 27-year-old woman with a 4-year history of etanercept and sulfasalazine treatment for rheumatoid arthritis was admitted with Stevens-Johnson syndrome. The patient received one dose of an OTC drug containing acetaminophen, phenylephrine and pheniramine two days prior to developing fist mucocutaneous symptoms. The most probable causative agent was paracetamol. Throughout the successful routine therapy of Stevens-Johnson syndrome etanercept therapy was continued. Sulfosalazin administration was stopped and administered again after recovery with no recurrence of the skin and mucosal symptoms.

Conclusions: This case indicates that there is no justification for discontinuation of long-term anti-TNF-alpha treatment in patients who develop Stevens- Johnson syndrome / toxic epidermal necrolysis.

Abstract Image

类风湿关节炎患者长期依那西普治疗期间的史蒂文斯-约翰逊综合征。
背景:依那西普和其他抗tnf - α药物已被认为是严重药物反应的治疗选择,包括史蒂文斯-约翰逊综合征和中毒性表皮坏死松解。依那西普已被证明能迅速减少表皮脱落,缩短愈合时间。还描述了依那西普引起的严重药物不良反应的病例。主要观察:一名27岁女性,接受依那西普联合柳氮磺胺治疗类风湿关节炎4年,因史蒂文斯-约翰逊综合征入院。患者在首次出现皮肤粘膜症状前两天服用了一剂含有对乙酰氨基酚、苯肾上腺素和苯那敏的非处方药。最可能的病原体是扑热息痛。在整个成功的史蒂文斯-约翰逊综合征的常规治疗过程中,依那西普治疗仍在继续。停用磺胺嘧啶,恢复后皮肤和粘膜症状无复发,重新给药。结论:该病例表明,史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症患者没有理由停止长期抗tnf - α治疗。
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