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Late-onset lupus: facts and fiction

机译:迟发性狼疮:事实与虚构

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As the world population ages, it is not uncommon to encounter patients who develop systemic lupus erythematosus (SLE) late in life. However, not much is known about SLE in this age group, but it clearly differs from younger onset disease in its epidemiologic, clinical and serological features; moreover, it is often misdiagnosed as drug-induced SLE or another rheumatic disease. As a result, a significant delay in its diagnosis is commonly observed. The choice of therapeutic agents in patients from this age group must also be very carefully considered. Immunosenescence, the development of CD8+ T-cell oligoclonal expansion and an abnormal apoptosis signaling pathway are some of the possible biologic mechanisms underlying late-onset SLE. Some misconceptions (fiction) are not uncommon in this subset of patients; they are gradually being replaced by facts as new data emerge.
机译:随着世界人口的老龄化,遇到生命晚期出现系统性红斑狼疮(SLE)的患者并不少见。然而,对于这个年龄段的SLE知之甚少,但是它的流行病学,临床和血清学特征与年轻的发病明显不同。此外,它经常被误诊为药物性SLE或另一种风湿病。结果,通常观察到其诊断的显着延迟。还必须非常仔细地考虑这个年龄组患者的治疗药物选择。免疫衰老,CD8 + T细胞寡​​克隆扩增的发展以及异常的细胞凋亡信号传导途径是迟发性SLE的潜在生物学机制之一。在这部分患者中,一些误解(小说)并不罕见。随着新数据的出现,它们逐渐被事实所取代。

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