Korean J Med > Volume 70(1); 2006 > Article
The Korean Journal of Medicine 2006;70(1):107-110.
Ja Kyoung Cho, Seok Jae Han, Jong Yup Bae, Seung Hie Chung, Chae Gi Kim, Jung Yoon Choe
서울대학교 의과대학 내과학교실, 간연구소
증례 : 전신성 홍반성 루푸스 환자에서 재발한 Kikuchi-Fujimoto disease (Case Reports : A case of recurrent Kikuchi-Fujimoto disease with SLE)
조자경, 한석재, 배종엽, 정승혜, 김채기, 최정윤
Abstract
Kikuchi-Fujimoto disease (KFD) is a rare self-limiting necrotizing lymphadenitis found mainly in young women. Patients typically present with lymphadenopathy and often with a high temperature. The etiology of the disease remains unknown, but various viral infection and autoimmune processes have been postulated to be the cause. One theory proposes that KFD may be a self-limiting form of systemic lupus erythematosus (SLE). This theory is strongly supported by the fact that microscopic features of KFD can be very similar to those found in lupus lymphadenitis. The diagnosis of KFD can precede, postdate or coincide with the diagnosis of SLE. No treatment is usually needed and relapse, although possible, is uncommon. Our case describes a young woman, originally diagnosed as having SLE, who subsequently developed recurrent KFD with axillary lymphadenopathy and fever.(Korean J Med 70:107-110, 2006) Key Words : Kikuchi-Fujimoto disease, Systemic lupus erythematosus
Key Words: Kikuchi-Fujimoto disease, Systemic lupus


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