Results 1 to 10 of about 4,842,015 (80)

Kikuchi-Fujimoto Disease in Pediatrics

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Background: Kikuchi-Fujimoto Disease (KFD)11 KFD: Kikuchi-Fujimoto Disease. is a rare, benign, idiopathic, and self-limiting lymphadenitis typically affecting head and neck regions.
Erna Kristiani   +4 more
doaj   +1 more source

Kikuchi-fujimoto disease [PDF]

open access: yesVojnosanitetski Pregled, 2003
Kikuchi-Fujimoto disease (KFD), also know as histiocytic necrotizing lymphadenitis, is a benign disorder characterized histologically by necrotic foci surrounded by histiocytic aggregates, and with the absence of neutrophils. KFD was recognized in Japan,
Đokić Milomir   +4 more
doaj   +1 more source

Hemophagocytic lymphohistiocytosis with recurrent Kikuchi-Fujimoto disease [PDF]

open access: yesYeungnam University Journal of Medicine, 2021
Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a self-limiting lymphadenitis. It is a benign disease mainly characterized by high fever, lymph node swelling, and leukopenia. Hemophagocytic lymphohistiocytosis (HLH)
Sang Min Lee   +5 more
doaj   +1 more source

Familial Kikuchi-Fujimoto disease [PDF]

open access: yesJournal of Clinical and Scientific Research, 2015
Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting disease of unknown aetiology presenting with cervical lymphadenopathy, fever, vomiting, weight loss, night sweats and chills. Familial occurrence of KFD is reported very rarely in literature.
Krishnappa J   +3 more
doaj   +1 more source

Kikuchi-fujimoto disease: A clinical enigma

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
doaj   +1 more source

KIKUCHI-FUJIMOTO DISEASE

open access: yesZdravniški Vestnik, 2008
BACKGROUND The Kikuchi Fujimoto disease (KFD) or histiocytic necrotising lymphadenitis is a rarebenign disease, more common in Japanese women. In other parts of the world and also inEurope the disease in rare.
Marjana Glaser   +2 more
doaj   +2 more sources

Doença de Kikuchi-Fujimoto Kikuchi-Fujimoto disease

open access: yesJornal Brasileiro de Pneumologia, 2008
A doença de Kikuchi-Fujimoto é caracterizada por febre e linfadenopatia, geralmente cervical. Esta doença acomete principalmente mulheres jovens. Pode ser confundida com linfoma, metástase de adenocarcinoma e tuberculose.
Rogério Gastal Xavier   +3 more
doaj   +1 more source

Kikuchi-Fujimoto disease

open access: yesJournal of Pathology of Nepal, 2012
Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a benign, self limited condition with higher prevalence among Japanese and other Asiatic people. Though the cause of this disease remains unclear, viral cause has been suggested.
RC Adhikari
doaj   +1 more source

Kikuchi-Fujimoto Disease: A Case Report

open access: yesKaohsiung Journal of Medical Sciences, 2003
We describe a rare but typical case of Kikuchi-Fujimoto disease (KFD). Two subcutaneous nodules appeared suddenly on the right of the neck of a 15-year-old girl.
Chih-Hung Lee, Shih-Tsung Cheng
doaj   +2 more sources

Kikuchi-Fujimoto disease

open access: yesOrphanet Journal of Rare Diseases, 2006
Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disorder, characterized by regional cervical lymphadenopathy with tenderness, usually accompanied with mild fever and night sweats.
Guilabert Antonio, Bosch Xavier
doaj   +1 more source

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