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模仿红斑狼疮(狼疮模仿者)的罕见疾病。

Rare diseases that mimic Systemic Lupus Erythematosus (Lupus mimickers).

机构信息

Service de dermatologie et d'allergologie, hôpital Tenon, AP-HP, 75020, Paris, France.

Immunoconcept, CNRS-UMR 5164, université de Bordeaux, 146, rue Léo-Saignat, 33076, Bordeaux, France; Centre hospitalier universitaire de Bordeaux, FHU ACRONIM, place Amélie-Raba-Léon, 33076, Bordeaux, France; Centre national de référence des maladies autoimmunes et systémiques rares Est Sud-Ouest (RESO)-LUPUS, 67000 Strasbourg, France.

出版信息

Joint Bone Spine. 2019 Mar;86(2):165-171. doi: 10.1016/j.jbspin.2018.10.007. Epub 2018 Oct 26.

Abstract

Several conditions have clinical and laboratory features that can mimic those present in Systemic Lupus Erythematosus (SLE). Some of these "SLE mimickers" are very common, such as rosacea which can be mistaken for the butterfly rash, while others such as Kikuchi disease, type-1 interferonopathies, Castleman's disease, prolidase deficiency, angioimmunoblastic T-cell lymphoma, Evans' syndrome in the context of primary immune deficiencies and the autoimmune lymphoproliferative syndrome are exceptionally uncommon. A proper diagnosis of SLE must therefore be based upon a complete medical history as well as on the adequate constellation of clinical or laboratory findings. While there is no single test that determines whether a patient has lupus or not, the search for auto-antibodies towards nuclear antigens is a key step in the diagnosis strategy, keeping in mind that ANAs are not specific for SLE. In case of persistent doubt, patients should be referred to reference centers with experience in the management of the disease.

摘要

有几种疾病的临床表现和实验室特征与系统性红斑狼疮(SLE)相似。其中一些“SLE 类同症”非常常见,如酒渣鼻可能被误诊为蝶形皮疹,而另一些疾病如菊池病、I 型干扰素病、Castleman 病、脯氨酸肽酶缺乏症、血管免疫母细胞性 T 细胞淋巴瘤、原发性免疫缺陷相关 Evans 综合征和自身免疫性淋巴组织增生综合征则非常罕见。因此,SLE 的正确诊断必须基于完整的病史以及充分的临床或实验室检查结果。虽然没有单一的测试可以确定患者是否患有狼疮,但寻找针对核抗原的自身抗体是诊断策略中的关键步骤,需要记住的是,ANA 并非 SLE 特异性。如果持续存在疑问,应将患者转介至具有该疾病管理经验的参考中心。

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