摘要
Dear Editor,Kikuchi-Fujimoto disease(KFD),or histiocytic necrotizing lymphadenitis,was initially described in 1972 by Drs.Kikuchi and Fujimoto(Shirakusa et al.,1988).The main clinical manifestations are fever and cervical lymphadenopathy with or without pain,sometimes accompanied by tachycardia,nausea and symptomatic infiltrative erythematous lesions.The diagnosis of KFD is usually based on characteristic lymph node histologic findings of coagulative necrosis,histiocytic infiltrate,loss of nodal architecture,
Dear Editor,Kikuchi-Fujimoto disease（KFD）,or histiocytic necrotizing lymphadenitis,was initially described in 1972 by Drs.Kikuchi and Fujimoto（Shirakusa et al.,1988）.The main clinical manifestations are fever and cervical lymphadenopathy with or without pain,sometimes accompanied by tachycardia,nausea and symptomatic infiltrative erythematous lesions.The diagnosis of KFD is usually based on characteristic lymph node histologic findings of coagulative necrosis,histiocytic infiltrate,loss of nodal architecture,
基金
supported in part by Beijing Natural Science Foundation (7162060 to ZX)
Basic and Clinic Science Foundation of Capital Medical University (16JL22 to ZX)
Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding (ZYLX201601 to LM)
Health and Family Planning Research and Development Foundation of Shunyi District (Wsjzkyfzzx-z-02 to ZX)
the US National Institutes of Health grant (P30-CA008748 to YWT)
