医学
塞库金单抗
白细胞减少症
泼尼松龙
银屑病性关节炎
内科学
皮肤病科
羟基氯喹
红斑狼疮
关节炎
蛋白尿
胃肠病学
多发性关节炎
免疫学
外科
化疗
抗体
疾病
2019年冠状病毒病(COVID-19)
传染病(医学专业)
肾
作者
Pedro Ávila-Ribeiro,Ana Rita Lopes,Joana Martins-Martinho,Estela Nogueira,Joana Antunes,José Carlos Romeu,Ana Rita Cruz-Machado,Elsa Vieira‐Sousa
出处
期刊:PubMed
日期:2023-10-15
卷期号:2 (3): 265-268
摘要
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.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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