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KMID : 0882420060710001138
Korean Journal of Medicine
2006 Volume.71 No. 0 p.1138 ~ p.1141
A case of histiocytic necrotizing lymphadenitis (Kikuchi¡¯s Disease) associated with adult onset Still¡¯s disease (AOSD)
Lee So-Young

Yun Sang-Pil
Song Han-Ul
Oh Ju-Hee
Kim Gwang-Il
Kim Tae-Heon
Hong Seung-Jae
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)
KEYWORD
Adult onset Still¡¯s disease, Histiocytic necrotizing lymphadenitis, Kikuchi¡¯s disease
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