Results 161 to 170 of about 2,941 (176)

The significance of T-BET-positive CD8 T-cells with diminished CD5 expression in Kikuchi-Fujimoto disease. [PDF]

J Clin Exp Hematop
Yamashita T, Momose S, Imada H, Takayanagi N, Murakami C, Nagata M, Sawada K, Yamazaki M, Shimizu T, Kikuchi Y, Yamamoto W, Higashi M.   +11 more
europepmc   +1 more source

Distinguishing Kikuchi-Fujimoto disease from lymphoma in patients by clinical and PET/CT features. [PDF]

Medicine (Baltimore)
Cheng MH, Xie LJ.
europepmc   +1 more source

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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

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

Kikuchi–Fujimoto Lymphadenopathy

2013
Kikuchi–Fujimoto (or Kikuchi) lymphadenopathy is a rare, regional, self-limited, necrotizing, histiocytic lymphadenitis that is frequently associated with mild fever and other systemic symptoms. Kikuchi et al., as well as Fujimoto et al., first described the disease independently in 1972 in the Japanese literature.
Roberto N. Miranda, Joseph D. Khoury, L. Jeffrey Medeiros   +2 more
openaire   +1 more source

Kikuchi‐Fujimoto disease in children

Journal of Paediatrics and Child Health, 2019
AimKikuchi‐Fujimoto disease (KFD) is an important cause of lymphadenitis in children. The primary aim of this study was to investigate the clinical characteristics of children with KFD and to assess the recurrence of this disease.MethodsThis is a retrospective study of patients younger than 18 years old, who were diagnosed with KFD from January 2000 to
Shoba N Selvanathan, Sharline Suhumaran, Vinay K Sahu, Chia Yin Chong, Natalie Woon Hui Tan, Koh Cheng Thoon   +5 more
openaire   +2 more sources

[Kikuchi-Fujimoto syndrome].

Ugeskrift for laeger, 2010
This article concerns a 25-year-old woman, with clinical symptoms of Kikuchi-Fujimoto Syndrome (KFS). The patient arrived ten days after symptom onset. She initially discovered lymphadenopathy on the right side of her neck. She had no fever, pruritus or weight loss.
Jamshaid, Ul-Mulk, Janko, Mortiz
openaire   +1 more source

Kikuchi-Fujimoto Disease

Infectious Diseases in Clinical Practice, 1999
Saba Medhane, Gary L. Simon
openaire   +1 more source