Results 61 to 70 of about 1,749 (155)

Recognition of Kikuchi–Fujimoto Disease in a Patient With Common Symptoms

open access: yesAnnals of Internal Medicine: Clinical Cases
A 33-year-old Afghan woman presented with intermittent headaches, fevers and chills, and unintentional weight loss. The physical examination was pertinent for a 2-cm tender right cervical lymphadenopathy.
Zainah Siddiqi   +4 more
doaj   +1 more source

Kikuchi-Fujimoto Disease

open access: yesMedical 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

Issue Information

open access: yes
Rheumatology &Autoimmunity, Volume 6, Issue 2, June 2026.
wiley   +2 more sources

Kikuchi-Fujimoto disease in 21-year-old man

open access: yesInternational Journal of Preventive Medicine, 2013
Kikuchi-Fujimoto disease also known as histiocytic necrotizing lymphadenitis is a benign disorder characterized histologically by necrotic foci surrounded by histiocytic aggregates, and with the absence of neutrophils.
Saeid Aminiafshar   +2 more
doaj  

Enfermedad de Kikuchi-Fujimoto: a propósito de un caso

open access: yesMedimay, 2013
La enfermedad de Kikuchi Fujimoto es una forma infrecuente de linfadenitis. En la actual provincia de Mayabeque (antes provincia de La Habana) no se recoge ningún caso con el referido diagnóstico. Se comunica una paciente femenina de 25 años, color de la
Bárbara Rodríguez Carrasco   +3 more
doaj   +4 more sources

Kikuchi–Fujimoto Disease Presenting as Brachial Plexus Neuritis: A Case Report

open access: yesIndian Journal of Neurosurgery, 2016
Kikuchi–Fujimoto disease is a rare, idiopathic, self-limiting necrotizing lymphadenitis of unknown etiology. It usually affects young Asian women. Clinically, it closely resembles with tuberculosis or lymphomas.
Rakesh Gupta   +2 more
doaj   +1 more source

Kikuchi-Fujimoto Disease as an Etiology for Relapsing/Remitting Fevers and Lymphadenopathy in a Patient With Dermatomyositis

open access: yesAnnals of Internal Medicine: Clinical Cases
Kikuchi-Fujimoto disease is a rare disease characterized by persistent fevers, tender lymphadenopathy, hyperinflammation, and histiocytic necrotizing lymphadenitis. It has been described in association with autoimmune disorders, primarily, systemic lupus
Danny Luan   +4 more
doaj   +1 more source

Kikuchi-Fujimoto disease: an unusual association with acute renal failure

open access: yesBrazilian Journal of Infectious Diseases, 2010
Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis of unknown etiopathogenesis, is a self-limited disease which frequently appears as feverish lymphadenomegaly, thus creating the need for differential diagnosis with lymphoma ...
Amanda Feliciano da Silva, MD   +4 more
doaj   +1 more source

KIKUCHI-FUJIMOTO DISEASE: CASE REPORT

open access: yesEurasian Journal of Medicine, 2019
Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis, is a unique form of self-limiting lymphadenitis and typically affects the head and neck regions. It usually occurs in young adults and has a female predilection.
Fazlı Erdoğan   +2 more
doaj  

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