Kikuchi-Fujimoto Disease의 치험례
A Case report of Kikuchi-Fujimoto Disease
장태화, 이상한, 권태건, 장현중, 김진수, 김진욱,
소속 상세정보
장태화 ( Jang Tae-Hwa ) - 경북대학교 치과대학 구강악안면외과학교실
이상한 ( Lee Sang-Han ) - 경북대학교 치과대학 구강악안면외과학교실
권태건 ( Kwon Tae-Geon ) - 경북대학교 치과대학 구강악안면외과학교실
장현중 ( Jang Hyun-Jung ) - 경북대학교 치과대학 구강악안면외과학교실
김진수 ( Kim Chin-Soo ) - 경북대학교 치과대학 구강악안면외과학교실
김진욱 ( Kim Jin-Wook ) - 경북대학교 치과대학 구강악안면외과학교실
KMID : 0360120070290060548
Abstract
Kikuchi-Fujimoto disease is a rare disease first described in 1972 by Kikuchi and Fujimoto et al. The disease is described as a benign and unusual self-limiting histiocytic necrotizing lymphadenitis of unknown origin, which is characterized histologically by necrotic foci surrounded by histiocytic aggregates, is usually manifested with lymphadenopathy and high fever. This disease mostly affects young Asian women between 20 and 30 years of age and has rarely been reported in children. Main symptoms are indolent or light tender, enlarged lymph nodes in the neck area. The correct diagnosis requires the histologic examination of the lymph node. Kikuchi-Fujimoto disease is easily confused histologically and clinically with lymphoma and systemic lupus erythematosis histologically and clinically. Although it is an uncommon cause of fever of unknown origin, early recognition of KFD is very important and will minimize potentially harmful and unnecessary evaluations and treatments. We reported a case, a 23-year old man who had Kikuchi-Fujimoto disease with a literature review.
키워드
Kikuchi; Fujimoto; Necrotizing Lymphadenitis; Karyorrhexis; Fever
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