late-onset systemic lupus erythematosus

  • 文章类型: Case Reports
    系统性红斑狼疮(SLE)是一种慢性,多系统自身免疫性疾病,可以在老年人身上表现出来,由于其非典型表现和合并症,提出了独特的诊断挑战。胸腔积液是SLE的一种相对少见的表现,研究表明,老年患者的患病率高于年轻患者。我们在此报告了一名75岁男性的典型延迟性SLE病例,该病例以左侧胸腔积液为首发表现。该病例强调了高龄患者诊断SLE的难度以及考虑广泛鉴别诊断的重要性。即使在可能暗示更常见的疾病的情况下。该病例还强调了一个事实,即单侧胸腔积液可以是SLE的初始表现,当胸腔积液的原因不清楚时,SLE应被视为潜在的诊断。
    Systemic lupus erythematosus (SLE) is a chronic, multisystem autoimmune disease that can manifest in older individuals, presenting unique diagnostic challenges because of its atypical presentations and comorbidities. Pleural effusion is a relatively uncommon manifestation of SLE, with studies suggesting a higher prevalence in older than younger patients. We herein report an atypical case of delayed-onset SLE in a 75-year-old man with left-sided pleural effusion as the initial presentation. This case underscores the difficulty of diagnosing SLE in patients of advanced age and the importance of considering a broad range of differential diagnoses, even in cases that may suggest a more common disease. This case also highlights the fact that unilateral pleural effusion can be an initial manifestation of SLE, and when the cause of the pleural effusion is unclear, SLE should be considered as a potential diagnosis.
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  • 文章类型: English Abstract
    一名74岁的男子出现左胸腔积液,怀疑患有良性石棉胸腔积液和结核性胸膜炎。由于胸腔积液中ADA水平升高,使用抗结核药物对结核性胸膜炎进行诊断性治疗.然而,右侧胸腔积液,皮肤/粘膜损伤,白细胞减少症,并出现发热升高。皮肤活检病理符合系统性红斑狼疮(SLE)。由于即使在停用所有药物后,临床结果也没有改善,他开始接受类固醇治疗,临床表现有所改善。他被怀疑患有迟发性SLE。总之,老年人出现胸腔积液时,也应鉴别狼疮胸膜炎。迟发性SLE和药物性狼疮应根据临床病程仔细区分。
    A 74-year-old man developed with left pleural effusion and was suspected of benign asbestos pleural effusion and tuberculous pleurisy. Because of elevation of ADA level in the pleural effusion, diagnostic treatment for tuberculous pleurisy by anti-tuberculosis drugs was performed. However, right pleural effusion, cutaneous/mucosal lesions, leukocytopenia, and fever elevation occurred. The pathology of skin biopsy was consistent with systemic lupus erythematosus (SLE). Since clinical findings did not improve even after discontinuation of all drugs, he received steroid therapy was started and clinical findings improved. He was suspected of late-onset SLE. In conclusion, lupus pleurisy should also be differentiated when pleural effusion is seen in older. Late-onset SLE and drug-induced lupus should be carefully differentiated based on the clinical course.
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  • 文章类型: Journal Article
    While functional decline is a common syndrome in geriatric medicine, the diagnosis of the underlying disease can be complex. We present a case of very late-onset systemic lupus erythematosus with fever, arthritis, lymphadenopathy, sicca syndrome, pleurisy, renal impairment and reversible functional and cognitive impairments. Prompt improvement was observed on prednisolone and hydroxychloroquine.
    UNASSIGNED: Systemic lupus erythematosus (SLE) rarely occurs in octogenarian patients.In such oldest old patients, SLE may predominantly present with subacute cognitive and functional impairments.Low-dose treatment (prednisolone 7.5 mg/day and hydroxychloroquine 5 mg/kg/day) can reverse all SLE manifestations within 1 month.
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  • 文章类型: Case Reports
    Lichen planus and lupus nephritis with late-onset systemic lupus erythematosus (LO-SLE) may occur concomitantly. However, coexistence of LO-SLE with focal segmental glomerulosclerosis and lichen planus has not been defined. In this article, we report a 57-year-old male patient presenting with lichen planus and focal segmental glomerulosclerosis who was subsequently diagnosed with LO-SLE. To the best of our knowledge, this is the first case of LO-SLE presenting with lichen planus and focal segmental glomerulosclerosis.
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