Results 51 to 60 of about 1,439 (150)
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
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 7, Page 983-987, July 2026.
Magí Brufau‐Cochs +7 more
wiley +1 more source
Kikuchi Disease of Parotid Gland
JBN (Jurnal Bedah Nasional)Aim: Kikuchi disease, often referred to as Kikuchi–Fujimoto disease (KFD), is an uncommon benign cervical lymphadenitis etiology. Cervical lymphadenopathy is Kikuchi disease's most prevalent clinical sign.
William Stevenson +2 more
doaj +1 more source
Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto).
Acta Médica Portuguesa, 2011 Kikuchi-Fujimoto disease, also called Histiocytic necrotizing lymphadentis, is a rare, benign and self-limited disease, with unknown etiology, that affects mainly young women, and is characterized by adenopathy (usually localized in the cervical region ...
Inês Antunes +8 more
doaj +1 more source
Kikuchi-Fujimoto disease in a young female with discoid lupus and alopecia
Chronic Diseases Journal, 2015 Kikuchi-Fujimoto disease is an uncommon, benign, autoimmune condition characterized by lymphadenopathy, fever, and neutropenia. It is a self-contained condition of unidentified etiology.
Shahla Afrasiabian +3 more
doaj +1 more source
Kikuchi-Fujimoto Disease Presenting as Autoimmune Limbic Encephalitis: A Case Report with Review of Literature. [PDF]
Ann Indian Acad NeurolKikuchi–Fujimoto disease (KFD) is a rare benign condition associated with fever and lymphadenopathy and was first described by Kikuchi and Fujimoto independently in 1972 as histiocytic necrotizing lymphadenitis.
Punith SB +7 more
europepmc +2 more sources
Kikuchi-Fujimoto disease: lymphadenopathy in siblings [PDF]
Canadian Medical Association Journal, 2010 A 19-year-old Aboriginal woman presented with a three-week history of swollen neck glands, nausea, vomiting, chills and weight loss. On examination, she had bilateral, nontender, diffuse cervical lymphadenopathy. Oral examination revealed extensive dental caries and periodontal disease.
Allison, Stasiuk +3 more
openaire +2 more sources
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
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
International Journal of Laboratory Hematology, Volume 47, Issue 5, Page 898-905, October 2025.This study investigates myeloperoxidase (MPO) in Kikuchi's disease, analyzing protein expression and mRNA levels in 43 patients. Results reveal 100% MPO protein positivity, elevated mRNA expression, and a positive correlation between mRNA and protein levels.
Chen Chang +4 more
wiley +1 more source