Results 11 to 20 of about 4,944,354 (189)
Kikuchi-Fujimoto disease [PDF]
Journal 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
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Kikuchi-Fujimoto disease [PDF]
Orphanet 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
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Kikuchi-fujimoto disease [PDF]
Vojnosanitetski 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
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Doença de Kikuchi-Fujimoto Kikuchi-Fujimoto disease
Jornal 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
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The co-occurrence of Kikuchi–Fujimoto disease and systemic lupus erythematosus: a case report
Journal of Medical Case Reports, 2023 Background Kikuchi–Fujimoto disease is an uncommon systemic disease that mostly affects young women. Kikuchi–Fujimoto disease typically manifests as necrotizing lymphadenopathy, which frequently follows by a fever; however, Kikuchi–Fujimoto disease ...
Maysam Yousefi +6 more
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Kikuchi-Fujimoto disease following SARS CoV2 vaccination: Case report
IDCases, 2021 Kikuchi's disease (KD) also known as Kikuchi-Fujimoto disease (KFD), or histiocytic necrotizing lymphadenitis was first described in 1972 independently by Kikuchi and Fujimoto et al. It is a benign self-limited condition of unknown etiology which usually
Hussam Al Soub +5 more
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Kikuchi-Fujimoto Disease [PDF]
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.
Soedibyo, Soepardi
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Kikuchi-Fujimoto Disease: A Review. [PDF]
Archives of Pathology & Laboratory Medicine, 2018 Kikuchi-Fujimoto disease (KFD) is a rare entity characterized by subacute necrotizing lymphadenopathy and frequently associated with fever. Young adults of Asian ancestry are most commonly affected, but it has been reported worldwide.
Anamarija M. Perry, Sarah M Choi
semanticscholar +3 more sources
Indian 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
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Kikuchi- Fujimoto Disease of Mesenteric Lymph Nodes Mimicking Acute Appendicitis
Journal of Nepal Medical Association, 2013 Kikuchi-Fujimoto disease, or histiocytic necrotising lymphadenopathy of unknown aetiology, is a rare, benign and self-limiting cause of lymphadenopathy often involving the cervical nodes, and rarely presenting with mesenteric lymphadenopathy.
Anne Shrestha +3 more
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