Results 171 to 180 of about 138,022 (200)

Behcet's Disease Presenting as Pancolonic Ulcerations in a Patient With Kikuchi-Fujimoto Disease: A Rare Gastrointestinal Manifestation. [PDF]

ACG Case Rep J
Lin F, Obeid A, Bhalala H, Patel N, Ge L, Modi R.   +5 more
europepmc   +1 more source

Kikuchi-Fujimoto hastalığı

Turk Otolarengoloji Arsivi, 2008
openaire   +1 more source

Kikuchi-Fujimoto Disease as a Cause of Recurrent Cervical Lymphadenopathy [PDF]

, 2015
Logan, Jennifer
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Kikuchi-Fujimoto Lymphadenitis

Advances in Anatomic Pathology, 2003
Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, was initially described as a distinct histologic pattern of lymphadenitis generally associated with a benign self-limited clinical course. While most common in Southeast Asia, where KFD was initially described in 1972 in young women, this lesion has since been reported
Mihaela, Onciu, L Jeffrey, Medeiros
openaire   +2 more sources

Childhood Kikuchi-Fujimoto disease

The Indian Journal of Pediatrics, 2009
To investigate the clinical features of Kikuchi-Fujimoto disease (KFD) and the relationship between viral infection and this disease in children will be better as Kikuchi-Fujimoto disease (KFD) is a lymphadenopathy. The aim of study is to investigate the clinical features of KFD and the relationship.
Chao Chun, Zou, Zheng Yan, Zhao, Li, Liang   +2 more
openaire   +2 more sources

A Rare Case of Kikuchi-Fujimoto Disease

Journal of Biomedical Research & Environmental Sciences
Kikuchi-Fujimoto Disease is a rare, benign, self-limiting cause of lymphadenopathy, typically characterized by fever and tender cervical lymph nodes, affecting mostly young women.
Pokhrel N, Paudyal S
semanticscholar   +1 more source

Kikuchi-Fujimoto Disease Revealing Lupus Nephritis: A Case Report in Sub-Saharan Africa

International Journal of Medical and Pharmaceutical Case Reports
Introduction:  Kikuchi-Fujimoto disease is a rare and benign condition. It most frequently affects young women. It manifests as predominantly cervical lymphadenopathy. Its diagnosis relies on lymph node histology, which reveals acidophilic necrosis, CD68+
S. M, D. K, Sassi Sh, Kane Bs, P. A
semanticscholar   +1 more source

Kikuchi Fujimoto disease

Pediatric Infectious Disease, 2015
Abstract Kikuchi Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis is an uncommon, idiopathic, generally self-limited cause of lymphadenitis. Kikuchi first described the disease in 1972 in Japan. Fujimoto and colleagues described Kikuchi's disease in the same year. The cause of Kikuchi-Fujimoto's disease is unknown.
Rajan J. Unadkat, Shaila R. Khubchandani, Ashish S. Gurjar   +2 more
openaire   +1 more source

Clinicopathological Features of Kikuchi-Fujimoto Disease: Retrospective Observational Study

Blood
Introduction: Kikuchi-Fujimoto disease (KFD), is a rare inflammatory disease of unknown etiology, typically presenting with transient fever and cervical lymphadenopathy.
Yoshito Nishimura, M. F. Nishimura, Chikako Sakao, Asami Nishikori, T. Habermann, A. Dispenzieri, Yasuharu Sato   +6 more
semanticscholar   +1 more source