Results 21 to 30 of about 138,022 (200)

Cytological Features of Kikuchi-Fujimoto Disease: A Multicenter Study of 30 Cases. [PDF]

open access: yesCureus
Background: Kikuchi-Fujimoto disease (KFD) is a frequently febrile, self-limited, subacute necrotizing lymphadenitis. It occurs predominantly in young females and is more common in Asia. Aim: This study aims to characterize the cytomorphological spectrum
Dwivedi M   +4 more
europepmc   +2 more sources

Human papilloma virus vaccine induced Kikuchi-Fujimoto disease: A case report. [PDF]

open access: yesLung India
Cervical lymphadenopathy can be due to numerous causes. The common causes include reactive and infections conditions in children and malignancy in the elderly. Kikuchi-Fujimoto disease (KFD) is a rare cause of cervical lymphadenopathy.
Shadrach BJ   +5 more
europepmc   +2 more sources

Serum Alkaline Phosphatase Levels in Pediatric Kikuchi-Fujimoto Disease: A Retrospective Observational Analysis. [PDF]

open access: yesImmun Inflamm Dis
Kikuchi‐Fujimoto disease (KFD) rarely affects pediatric patients and is characterized by prolonged fever and cervical lymphadenopathy. The diagnosis of KFD remains challenging and often requires an invasive biopsy.
Fujiwara S, Higuchi Y, Shimizu J.
europepmc   +2 more sources

A Kikuchi-Fujimoto syndrome in the pocket of a non-Hodgkin lymphoma: case report with a mini-review of the literature. [PDF]

open access: yesAnn Med Surg (Lond)
Introduction: Kikuchi–Fujimoto disease is a rare, benign necrotizing lymphadenitis primarily affecting young women. Case presentation: We present the case of a 26-year-old female patient with no notable medical history, who developed a persistent right ...
Bouchlarhem S   +4 more
europepmc   +2 more sources

Pediatric Kikuchi-Fujimoto Disease: Case Report and Review of Cutaneous and Histopathologic Features in Childhood. [PDF]

open access: yesDermatopathology (Basel)
Kikuchi–Fujimoto disease (KFD) is a rare condition characterized by necrotizing lymphadenitis and fever, often associated with immune dysregulation. Histologically, it features necrotic foci with abundant histiocytes and plasmacytoid dendritic cells but ...
Soto-Moreno A   +7 more
europepmc   +2 more sources

Kikuchi-Fujimoto Disease: A Case Series and Review of the Literature. [PDF]

open access: yesDiseases
Kikuchi–Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, self-limiting disorder characterized by fever typically lasting for 1 week up to 1 month and painful necrotizing lymphadenopathy, primarily affecting young ...
Deb A   +6 more
europepmc   +2 more sources

Kikuchi-Fujimoto Disease

open access: yesIndian Pediatrics Case Reports, 2021
Background: Kikuchi Fujimoto disease (KFD) is a rare, benign self-limited disease characterized by prolonged regional lymphadenopathy associated with or without systemic signs or symptoms. It is a rare diagnosis in children.
Sangeeta Priyadarshi Sawant   +3 more
openaire   +4 more sources

Enfermedad de Kikuchi en joven masculino sin antecedentes médicos. Causa inusual de fiebre de origen desconocido. Presentación de caso

open access: yesCiencia y Salud, 2021
Introducción: la enfermedad de Kikuchi, también llamada enfermedad Kikuchi–Fujimoto o linfadenitis necrotizante histiocítica es una condición benigna de etiología incierta que usualmente se presenta como fiebre de origen desconocido (FOD).
Elianet Castillo, Claudia Blanco
doaj   +1 more source

Kikuchi–Fujimoto disease: literature review and report of four cases

open access: yesОнкогематология, 2022
Kikuchi–Fujimoto disease, or necrotizing histiocytic lymphadenitis, is one of the rare causes of benign lymphadeno-pathy. The diagnosis is based on histological and immunohistochemical analysis of the lymph node biopsy. The article presents four clinical
V. G. Potapenko   +5 more
doaj   +1 more source

Kikuchi-Fujimoto Disease

open access: yesArchives of Pathology & Laboratory Medicine, 2010
Abstract Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a self-limited condition, characterized by benign lymphadenopathy with associated fevers and systemic symptoms. It most commonly affects adults younger than 40 years of age and of Asian descent. Involved lymph nodes demonstrate paracortical areas of apoptotic
Charles Blake, Hutchinson, Endi, Wang
openaire   +4 more sources

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