Results 61 to 70 of about 2,941 (176)
Revista Brasileira de Oftalmologia, 2008 Apresentação de um caso de febre de origem obscura numa paciente feminina de 35 anos, com queda do estado geral, adenomegalia cervical posterior, monilíase oral, parotidite e irite.Após o parecer oftalmológico, o tratamento foi iniciado e posteriormente ...
Marco Aurelio Varella Figueiredo +2 more
doaj +1 more source
Doença de Kikuchi e Fujimoto [PDF]
, 2005 A doença de Kikuchi e Fujimoto, também conhecida como Linfadenite Histiocítica Necrosante, é uma entidade clínico-patológica rara cuja etiologia permanece desconhecida; tem sido sugerida a possibilidade de uma etiologia auto-imune, mas também tem sido ...
Almeida, T +4 more
core
A Case of Relapsing Kikuchi-Fujimoto Disease [PDF]
, 2013 Kikuchi-Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis was first described in Japan in 1972. It is described as a benign syndrome most commonly involving cervical lymphadenopathy, fever, and night sweats.
Carroll, Matthew B. +3 more
core +2 more sources
[Kikuchi-Fujimoto disease]. [PDF]
La Revue de medecine interne, 2011 Kikuchi-Fujimoto disease is a necrotizing lymphadenitis, involving young patients, predominantly females. Lymphadenopathy is usually localized, particularly in the cervical area, mostly unilateral and tender. Fever is present in one third of cases. Associated skin lesions, arthralgia, myalgia, splenomegaly or hepatomegaly are rare.
openaire +3 more sources
Kikuchi‐Fujimoto disease: A rare case report from Nepal
Clinical Case Reports, 2021 Clinicians and pathologists must be aware of the occurrence of Kikuchi‐Fujimoto Disease, as one of the differential diagnoses of cervical lymphadenopathy.
Rahul Rauniyar +6 more
doaj +1 more source
Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi +5 more
wiley +1 more source
A Kikuchi-Fujimoto Disease Case Mimicking T Cell Lymphoma with Prolonged Fever [PDF]
, 2014 Kikuchi-Fujimoto disease (KFD) is a self-limited disease characterized by necrotizing lymphadenitis. Although cervical lymphadenitis in young women is the most familiar clinical presentation, it may take place in the etiology of fever in cases presenting
Ilker Inanc Balkan +2 more
core +3 more sources
Medical Journal of Indonesia, 2005 Kikuchi-Fujintoto disease (KFD) was first reported by 2 Japanese pathologists, Kikuchi and Fujimoto, independently in 1972. KFD is an idiopathic, self-limited necrotizing lymphadenitis. The most common clinical manifestation is cervical lymphadenopathy accompanied by fever, myalgia, leukopenia, and skin rash.
openaire +2 more sources
Necrotizing Histiocytic Lymphadenitis: Report of two cases (Kikuchi-Fujimoto disease)
مجله دانشگاه علوم پزشکی گرگان, 2004 Kikuchi-Fujimoto disease is a necrotizing Lymphadenitis with benign self-limit process in young women with fever, cervical lymphadenopathy and increased ESR with leukopenia. In this report we introduce 2 females with Kikuchi-Fujimoto disease.
M.Sharbatdaran (MD) +2 more
doaj
Cytometry Part B: Clinical Cytometry, Volume 108, Issue 6, Page 430-447, November 2025.Abstract The diagnosis of T‐cell neoplasms remains one of the most challenging areas in hematopathology due to the immunophenotypic heterogeneity and subtle aberrancies often present in these entities. This “Best Practice” manuscript provides a practical framework for laboratories to design, validate, and interpret immunophenotyping studies of immature
Jean Oak +10 more
wiley +1 more source