histiocytic necrotizing lymphadenitis

histiocytic necrotizing lymphadenitis

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Clinical Characteristics of Severe Histiocytic Necrotizing Lymphadenitis (Kikuchi-Fujimoto Disease) in Children.
Histiocytic necrotizing lymphadenitis in the context of systemic lupus erythematosus (SLE): Is histiocytic necrotizing lymphadenitis in SLE associated with skin lesions?
Kikuchi-Fujimoto disease (KFD) is histiocytic necrotizing lymphadenitis, first described by Dr Masahiro Kikuchi in 1972 in Japan.
Treatment of histiocytic necrotizing lymphadenitis (Kikuchi's disease) with prolonged fever by a single course of methylprednisolone pulse therapy without maintenance therapy: experience with 13 cases.
Kikuchi-Fujimoto Disease (KFD), also known as histiocytic necrotizing lymphadenitis, was described in Japan, in 1972, by Kikuchi and Fujimoto (1,2) simultaneously.
Kikuchi disease is also known as Kikuchi-Fujimoto disease and histiocytic necrotizing lymphadenitis.
Kikuchi-Fujimoto disease (KFD), or histiocytic necrotizing lymphadenitis, was first described in 1972 simultaneously by Kikuchi (1) and Fujimoto and colleagues (2) as a lymphadenitis with focal proliferation of histiocytic cells and abundant karyorrhectic debris.
A study of the viral etiology of histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease).
Child fatality associated with pathological features of histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease).
Kikuchi's disease is a self-limiting entity of unknown etiology that is also known as cervical subacute necrotizing lymphadenitis, histiocytic necrotizing lymphadenitis, and other terms.

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