Beernaert Laetitia, Vanderhulst Julien
Department of Geriatrics, Erasme Hospital, Free University of Brussels (ULB), Brussels, Belgium.
Department of Internal Medicine, Brugmann University Hospital, Free University of Brussels (ULB), Brussels, Belgium.
Am J Case Rep. 2020 Dec 22;21:e927929. doi: 10.12659/AJCR.927929.
BACKGROUND Antithyroid drugs, namely methimazole, are well-known causes of drug-induced lupus erythematosus. This is, however, an infrequent adverse effect. Selective Immunoglobulin A (IgA) deficiency, in contrast, is the most common primary immunodeficiency. Patients with IgA deficiency are at risk of developing infectious diseases, but also autoimmune diseases such as Grave's disease or systemic lupus erythematosus. CASE REPORT We report a case of methimazole-induced lupus erythematosus in a 32-year-old man with renal involvement and concomitant selective IgA deficiency. Symptoms promptly resolved after treatment with hydroxychloroquine and corticosteroids after discontinuation of methimazole. Lupus nephritis required treatment with cyclophosphamide followed by maintenance therapy with mycophenolate mofetil. CONCLUSIONS Drug-induced lupus erythematosus usually develops after a few months or years of exposure to the causative agent. No specific symptoms exist. The diagnosis is not based on particular specific tests, but relies on a set of arguments evoking the role of the medication inducing the condition. The first step in treatment is to stop the causative drug. The therapeutic management of the various manifestations does not differ from that of idiopathic systemic lupus erythematosus. We briefly discuss the relationship between drug-induced lupus erythematosus, Grave's disease, and IgA deficiency, and suggest that IgA deficiency may act as a potential risk factor. Testing for IgA deficiency could be helpful in patients being treated with drugs known to be associated with drug-induced lupus erythematosus.
背景 抗甲状腺药物,即甲巯咪唑,是药物性红斑狼疮的常见病因。然而,这是一种罕见的不良反应。相比之下,选择性免疫球蛋白A(IgA)缺乏是最常见的原发性免疫缺陷。IgA缺乏的患者不仅有发生传染病的风险,还易患自身免疫性疾病,如格雷夫斯病或系统性红斑狼疮。病例报告 我们报告一例32岁男性患者,因服用甲巯咪唑诱发红斑狼疮,伴有肾脏受累及选择性IgA缺乏。停用甲巯咪唑后,经羟氯喹和皮质类固醇治疗,症状迅速缓解。狼疮性肾炎需用环磷酰胺治疗,随后用霉酚酸酯维持治疗。结论 药物性红斑狼疮通常在接触致病药物数月或数年后发生。没有特定症状。诊断并非基于特定的检测,而是依赖于一系列提示药物诱发该病的依据。治疗的第一步是停用致病药物。各种表现的治疗管理与特发性系统性红斑狼疮无异。我们简要讨论了药物性红斑狼疮、格雷夫斯病和IgA缺乏之间的关系,并提示IgA缺乏可能是一个潜在风险因素。对于正在接受已知与药物性红斑狼疮相关药物治疗的患者,检测IgA缺乏可能会有帮助。