Golimumab-exacerbated subacute cutaneous lupus erythematosus.

Eric Wilkerson, Matthew A Hazey, Soon Bahrami, Jeffrey P Callen
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引用次数: 23

Abstract

Background: Subacute cutaneous lupus erythematosus (SCLE) is characterized by annular, nonscarring, photodistributed, or papulosquamous lesions. The disease may be idiopathic, drug induced, or drug exacerbated.

Observations: A 66-year-old woman with a history of hypertension, parkinsonism, rheumatoid arthritis, anxiety and depression, and symptoms of Sjögren syndrome was seen with a 1-month history of an eruption on her upper extremities and upper trunk. The eruption had begun 2 to 3 weeks after subcutaneous injection of golimumab for rheumatoid arthritis. She had developed SCLE 2 years previously due to furosemide use and 10 years previously due to hydrochlorothiazide use. Physical examination revealed scaly, annular, erythematous plaques photodistributed on the arms, legs, and upper trunk. A punch biopsy specimen demonstrated vacuolar interface dermatitis and lymphohistiocytic perivascular inflammation. Serological abnormalities included a positive antinuclear antibody, an elevated anti-La/SS-B antibody level, and an elevated anti-Ro/SS-A antibody level. She was diagnosed as having SCLE and was initially treated with desonide lotion, photoprotection, prednisone (40 mg/d) tapered over 6 weeks, and hydroxychloroquine sulfate (200 mg twice daily). Because of persistent disease, methotrexate sodium (12.5 mg/wk) was subsequently added to the regimen, and her eruption cleared completely.

Conclusions: Golimumab should be added to the list of medications capable of inducing or exacerbating SCLE. Our patient demonstrated variable times to the resolution of SCLE, possibly attributable in part to the different half-lives of the agents administered.

戈利单抗加重亚急性皮肤红斑狼疮。
背景:亚急性皮肤红斑狼疮(SCLE)以环状、无瘢痕、光分布或丘疹状鳞状病变为特征。这种疾病可能是特发性的、药物诱发的或药物加重的。观察:66岁女性,有高血压、帕金森病、类风湿关节炎、焦虑和抑郁病史,Sjögren综合征症状,上肢和上躯干有1个月的皮疹病史。皮下注射golimumab治疗类风湿关节炎2 - 3周后开始出现皮疹。她在2年前因使用速尿而发展为sle, 10年前因使用氢氯噻嗪而发展为sle。体格检查显示鳞状环状红斑斑光分布于手臂、腿部和上肢。穿刺活检标本显示空泡界面皮炎和淋巴组织细胞血管周围炎症。血清学异常包括抗核抗体阳性,抗la /SS-B抗体水平升高,抗ro /SS-A抗体水平升高。她被诊断为SCLE,最初接受地奈德洗剂、光保护、强的松(40 mg/d)和硫酸羟氯喹(200 mg,每日两次)6周逐渐减少治疗。由于病情持续,随后在治疗方案中加入甲氨蝶呤钠(12.5 mg/周),她的皮疹完全消失。结论:应将Golimumab添加到能够诱导或加重SCLE的药物列表中。我们的患者表现出不同的时间来解决SCLE,可能部分归因于不同的半衰期的药物施用。
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来源期刊
Archives of dermatology
Archives of dermatology 医学-皮肤病学
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4-8 weeks
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