Results 91 to 100 of about 138,022 (200)
Cureus, 2023 Kikuchi-Fujimoto Disease (KFD), or histiocytic necrotizing lymphadenitis (HNL), is a rare self-limiting disorder presenting with fever and swollen lymph nodes.
Muhammad Burhan Majeed Rana +6 more
semanticscholar +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
Kikuchi-Fujimoto disease following SARS-CoV-2 infection: A rare disease with increased incidence during the COVID-19 pandemic? [PDF]
Respirol Case RepKikuchi‐Fujimoto Disease (KFD), also known as Kikuchi disease or Kikuchi histiocytic necrotizing lymphadenitis, is a rare and self‐limiting condition characterized by cervical lymphadenopathy and fever, primarily affecting young Asian adults.
Leung CCD +7 more
europepmc +2 more sources
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: a case report and the evaluation of diagnostic procedures
BMC Oral Health, 2019 Background Kikuchi-Fujimoto disease, known as histiocytic necrotizing lymphadenitis, is a benign, self-limiting and systemic disorder involving lymph nodes with unknown aetiology.
Shenjie Xu, Weilian Sun, Jiamei Liu
doaj +1 more source
Heterozygous germline TET2 loss‐of‐function variants associated with an ALPS‐like phenotype
British Journal of Haematology, Volume 206, Issue 5, Page 1330-1334, May 2025.Summary Germline homozygous loss‐of‐function mutations in TET2 result in significant childhood immunodeficiency that resembles autoimmune lymphoproliferative syndrome and predisposes one to lymphoma. The implications of heterozygous variants are less well understood.
Sean Harrop +13 more
wiley +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
Parinaud Oculoglandular Syndrome as a Prominent Presenting Feature of Kikuchi-Fujimoto Disease – A Case Report and Review of the Literature [PDF]
, 2011 Kikuchi-Fujimoto disease (KFD) is an often under-diagnosed form of lymphadenitis that clinically mimics lymphoma. Ocular manifestations are rare in patients with KFD and are under-appreciated in the literature.
Bala, MD, PhD, Kamalesh K. +3 more
core +1 more source