Secukinumab诱导的银屑病关节炎系统性红斑狼疮。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY
ARP Rheumatology Pub Date : 2023-07-01
Pedro Ávila-Ribeiro, Ana Rita Lopes, Joana Martins-Martinho, Estela Nogueira, Joana Antunes, José Carlos Romeu, Ana Rita Cruz-Machado, Elsa Vieira-Sousa
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引用次数: 0

摘要

病例报告:一名68岁男性,因新冠肺炎疫情,接受secukinumab治疗银屑病关节炎,暂停治疗三个月。再次使用secukinumab后,出现厌食症和体重减轻,四个月后,他突然出现低烧、疲劳、流感样症状、呼吸困难和广泛的炎症性关节痛。实验室调查显示,新发性贫血、白细胞减少、淋巴细胞减少、细胞溶血、急性期反应物升高、C3补体消耗、蛋白尿(1630mg/24h)、活性尿沉渣、抗核抗体阳性(1:1280)和抗双链DNA抗体(212.3IU/mL)。胸部影像学表现为周围性肺栓塞、大叶性肺炎和少量双侧胸腔积液。怀疑是药物引起的红斑狼疮(DILE),患者已住院治疗。赛库金单抗停用,开始依诺肝素、抗生素、依那普利、羟氯喹和泼尼松龙0.5mg/kg qd治疗。一个月后,除蛋白尿(降至653mg/24小时)外,临床和实验室症状均得到缓解。假定为增殖性狼疮性肾炎,并引入霉酚酸酯,在33个月的随访中持续完全缓解。讨论:这是第二例报告的系统性secukinumab相关DILE病例,也是第一例肾脏受累病例。回顾DILE的临床和实验室特征,并与先前描述的病例进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Secukinumab-induced systemic lupus erythematosus in psoriatic arthritis.

Case report: A 68-year-old male treated with secukinumab for psoriatic arthritis suspended treatment for three months due to COVID pandemic. Upon secukinumab reintroduction, anorexia and weight loss ensued and four months later he had an abrupt onset of low-grade fever, fatigue, flu-like symptoms, dyspnoea and widespread inflammatory arthralgias. Laboratory investigations showed de novo anaemia, leukopenia, lymphopenia, cytocholestasis, elevated acute phase reactants, C3 complement consumption, proteinuria (1630mg/24h), active urine sediment, positive antinuclear (1:1280) and anti-double-stranded DNA (212.3 IU/mL) antibodies. Chest imaging showed peripheral pulmonary embolism, lobar pneumonia, and a small bilateral pleural effusion. Drug-induced lupus erythematosus (DILE) was suspected, and the patient was hospitalised. Secukinumab was discontinued and treatment with enoxaparin, antibiotics, enalapril, hydroxychloroquine and prednisolone 0.5mg/kg qd was started. Clinical and laboratorial remission ensued after one month except for proteinuria (decreased to 653mg/24h). Proliferative lupus nephritis was assumed and mycophenolate mofetil was introduced, with sustained complete remission over a 33-month follow-up.

Discussion: This is the second reported case of systemic secukinumab-associated DILE, and the first with renal involvement. Clinical and laboratory features of DILE are reviewed and compared with previously described cases.

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