Infectious facade of autoimmunity: when SLE masquerades as tuberculosis.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Debashis Priyadarshan Sahoo, Bhupen Barman, Md Jamil, Gwenette Andrea War, Annu Gupta, Ashwini Chikkannaswamy
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引用次数: 0

Abstract

Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder characterised by widespread inflammation affecting multiple organ systems. Its varied clinical manifestations often complicate diagnosis, as it can closely mimic other conditions, particularly infectious diseases such as tuberculosis. This case report describes a woman in her early 20s initially suspected of having disseminated tuberculosis and treated accordingly due to overlapping symptoms, including fever, night sweats, lymphadenopathy and bilateral exudative pleural effusion. Subsequent evaluation, however, confirmed a diagnosis of SLE based on clinical criteria and positive autoantibody results. The patient also presented with anaemia of chronic disease and elevated inflammatory markers. This case highlights the diagnostic difficulty of differentiating SLE from tuberculosis, particularly in regions with high tuberculosis prevalence. Comprehensive physical examination, thorough evaluation and consideration of autoimmune disorders are essential in such cases to ensure accurate diagnosis, guide appropriate treatment and prevent severe complications.

自身免疫的感染表象:SLE伪装成肺结核。
系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,其特征是影响多器官系统的广泛炎症。其多样的临床表现往往使诊断复杂化,因为它与其他疾病,特别是结核病等传染病非常相似。本病例报告描述了一名20岁出头的女性,最初怀疑患有播散性肺结核,并因发烧、盗汗、淋巴结病和双侧渗出性胸腔积液等重叠症状而接受相应治疗。然而,随后的评估根据临床标准和自身抗体阳性结果证实了SLE的诊断。患者还表现为慢性疾病贫血和炎症标志物升高。本病例突出了鉴别SLE与结核病的诊断困难,特别是在结核病高发地区。在这种情况下,全面的体格检查、彻底的评估和自身免疫性疾病的考虑是必不可少的,以确保准确的诊断、指导适当的治疗和预防严重的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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