Results 61 to 70 of about 8,209 (172)
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
Association of IL-10 receptor 2 (IL10RB) SNP with systemic sclerosis [PDF]
, 2008 Interleukin-10 (IL-10) signaling has been suggested to play a role in systemic sclerosis (SSc). IL10RB codes for IL-10 receptor 2 (IL-10R2), a component shared in receptor complexes for IL-10, IL-22, IL-26 and interferon (IFN)-λ.
Ehara Yukikazu +10 more
core +1 more source
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
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
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
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
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
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
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Neuropsychopharmacology Reports, Volume 45, Issue 3, September 2025.Mental health mediates the association between physical disease and subjective health‐related quality of life (QOL), and between inflammatory cytokines and subjective health‐related QOL. Anti‐inflammatory cytokines are activated by physical disease severity and have a protective effect on mental health.
Kazuyuki Nakagome +15 more
wiley +1 more source
Malaltia de Kikuchi-Fujimoto: presentació d'un cas pediàtric [PDF]
, 2017 Introducció. La malaltia de Kikuchi-Fujimoto, o limfadenitis necrosant histiocítica, és una patologia benigna poc freqüent que es caracteritza per clínica de febre i limfadenopatia cervical.
Colomo Saperas, Lluís +5 more
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