The Korean Journal of Internal Medicine

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Original Article
Korean J Med. 2006;71(3):1138-1141.
증례 : 성인형 스틸병과 동반된 조직구성 괴사성 림프절염 1예
이소영&#;윤상필&#;송한얼&#;오주희&#;김광일&#;김태헌&#;홍승재, , , , , ,
Department of Internal Medicine, Ewha Womans University School of Medicine, Seoul, Korea
A case of histiocytic necrotizing lymphadenitis (Kikuchi’s Disease) associated with adult onset Still’s disease (AOSD)
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이화여자대학교 의과대학 내과학교실


Abstract
Histiocytic necrotizing lymphadenitis (Kikuchi's disease) is the benign self limiting disease of an unknown origin. It causes painful lymphadenopathy with frequent fever, and it usually occurs in young adults. Adult onset Still's disease (AOSD) is a rare disorder of an unknown origin, and it's characterized by high spiking fever, polyarthritis/polyarthralgia, evanescent erythematous maculopapular rash, leukocytosis and the involvement of various organs. We have experienced a case of 34-year-old woman with AOSD and histiocytic necrotizing lymphadenitis. Considering that no definite etiology has been established for both disorders, the coexistence of both conditions in this patient suggests the possibility that they share a common immunologic pathway.(Korean J Med 71:S1138-S1141, 2006)

Keywords :Adult onset Still's disease, Histiocytic necrotizing lymphadenitis, Kikuchi's disease
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