儿童期发病的系统性红斑狼疮,可能由严重急性呼吸综合征冠状病毒2感染引发,表现为自身免疫性溶血性贫血

Abdul Rauf, S. Thekkudan, N. Mampilly, A. Vijayan
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引用次数: 2

摘要

系统性红斑狼疮(SLE)是一种临床表现多样的多系统慢性自身免疫性疾病。在遗传易感患者中,各种感染因子在触发疾病发作中的作用与SLE的发病机制有关。据报道,严重急性呼吸综合征冠状病毒2可引发多种自身免疫性疾病,包括少数成年人的SLE。在此,我们报告了一名之前身体健康的12岁女孩,在COVID-19检测呈阳性3周后出现温热抗体库姆斯阳性自身免疫性溶血性贫血。COVID - IgG抗体检测阳性。在住院期间,她出现多系统受累,表现为神经系统表现和关节炎。给予类固醇、静脉注射免疫球蛋白和支持措施。她的抗核抗体和抗dsdna抗体呈阳性,补体水平低,确诊为SLE。患者的临床状况迅速改善,神经功能正常,系列血红蛋白呈改善趋势。静脉注射类固醇改为口服,并加入羟氯喹。在3周的随访中,她保持良好。
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Childhood-onset systemic lupus erythematosus, probably triggered by severe acute respiratory syndrome coronavirus 2 infection, presenting with autoimmune haemolytic anaemia
Systemic lupus erythematosus (SLE) is a multisystemic and chronic autoimmune disease with varying clinical manifestations. The role of various infectious agents in triggering the disease onset in genetically predisposed patients has been implicated in the pathogenesis of SLE. The severe acute respiratory syndrome coronavirus 2 has been reported to trigger various autoimmune diseases including SLE in few adults. Herein, we report the case of a previously well 12-year-old girl who presented with warm antibody Coombs-positive autoimmune haemolytic anaemia, 3 weeks after testing positive for COVID-19. COVID IgG antibody test was positive. During the hospital stay, she developed multisystem involvement in the form of neurological manifestations and arthritis. She was managed with steroids, intravenous (IV) immunoglobulins and supportive measures. Her anti-nuclear antibody and anti-dsDNA antibodies were positive and complement levels were low, confirming a diagnosis of SLE. Her clinical condition improved rapidly and remained neurologically normal, and serial haemoglobin showed an improving trend. IV steroids were changed to oral form, and hydroxychloroquine was also added. She remained well on 3-week follow-up.
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