医学
病因学
疾病
皮肤病科
鉴别诊断
病理
组织细胞
系统性狼疮
红斑狼疮
人口
系统性红斑狼疮
免疫学
抗体
环境卫生
作者
Barbara Ruaro,Alberto Sulli,Elisa Alessandri,Giulio Fraternali Orcioni,Maurizio Cutolo
出处
期刊:Lupus
[SAGE]
日期:2014-04-16
卷期号:23 (9): 939-944
被引量:29
标识
DOI:10.1177/0961203314530794
摘要
Kikuchi–Fujimoto’s disease (KFD), or histiocytic necrotizing lymphadenitis, is a benign and self-limiting disease of unknown aetiology. KFD tends to affect a young population under 30 years of age and predominantly females. KFD is a rare pathology and its association with systemic lupus erythematosus (SLE) is not frequent. Herein, we present the case of a male Italian patient with SLE in association with KFD with 5 years of follow-up, where a differential diagnosis from infection or lymphoproliferative disease was problematic.
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