نتایج جستجو برای: fujimoto disease

تعداد نتایج: 1490358  

2015
Xavier Bosch Antonio Guilabert

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. Less frequent symptoms include weight loss, nausea, vomiting, sore throat. Kikuchi-Fujimoto disease is an extremely rare disease known to have a worldwide distribution with higher prevalence among Japanese...

Journal: :Journal of Clinical and Experimental Investigations 2011

Journal: :International Journal of Clinical Medicine 2015

2015
Kandukuri Mahesh Kumar V. Indira V. Hari Shanker

Kikuchi-Fujimoto disease (KFD) benign, systemic lymphadenitis, self limiting disease Pathologists Kikuchi and Fujimoto in Japan in 1972. The incidence of KFD is unknown. KFD is up to 4 times commoner in women. It presents as lymphadenopathy mainly involving the cervical region, but can occur in any lymph node and even in extra nodal sites. Fever is associated with lymph node enlargement in half...

2016
Kelly S. Rue Damien C. Rodger Narsing A. Rao

Purpose We present a patient with systemic lupus erythematosus with significant vaso-occlusive retinal findings mimicking antiphospholipid antibody syndrome, who developed Kikuchi-Fujimoto disease. Observations Our patient was initially diagnosed with systemic lupus erythematosus with antiphospholipid antibody syndrome given consistent serologic markers and profound retinal vascular ischemia....

2012
Ram Chandra Adhikari

Correspondence: Dr. Ram Chandra Adhikari, MD Consultant Pathologist, Department of Pathology, Om Hospital & Research Centre, Kathmandu, Nepal GPO Box: 2496 E-mail: [email protected] 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 unc...

2012
Al-Bishri Jamal

In order to determine the clinical significance of Kikuchi Fujimoto Disease (histiocytic necrotizing lymhadenitis) and to review the literature available on this condition, we selected the Medicine research papers in English language published between the years 1972 to 2011.Kikuchi Fujimoto Disease (KFD) is an uncommon, cosmopolitan, benign and self-limiting condition with higher Japanese and A...

Journal: :Orphanet Journal of Rare Diseases 2004
Xavier Bosch Antonio Guilabert

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. Less frequent symptoms include weight loss, nausea, vomiting, sore throat. Kikuchi-Fujimoto disease is an extremely rare disease known to have a worldwide distribution with higher prevalence among Japanese...

2014
Guillaume Dumas Virginie Prendki Julien Haroche Zahir Amoura Patrice Cacoub Lionel Galicier Olivier Meyer Christophe Rapp Christophe Deligny Bertrand Godeau Elisabeth Aslangul Olivier Lambotte Thomas Papo Jacques Pouchot Mohamed Hamidou Claude Bachmeyer Eric Hachulla Thierry Carmoi Robin Dhote Magdalena Gerin Arsene Mekinian Jérôme Stirnemann Fréderic Charlotte Dominique Farge Thierry Molina Olivier Fain

Kikuchi-Fujimoto disease (KFD) is a rare cause of lymphadenopathy, most often cervical. It has been mainly described in Asia. There are few data available on this disease in Europe. We conducted this retrospective, observational, multicenter study to describe KFD in France and to determine the characteristics of severe forms of the disease and forms associated with systemic lupus erythematosus ...

Journal: :Internal medicine 2011
Yasushi Yoshida Yasuo Matsuzawa Hagino Rikitake Toru Wakabayashi Noriaki Okada Toshihisa Kuroda Kengo Kawashima Masaaki Tanabe Nobuyuki Hiruta Makoto Nagashima Tatsuo Kawashima

A 44-year-old man was referred to our hospital because of persistent high fever. Both CT and PET-CT demonstrated lymph node lesions limited to the mediastinal region without cervical lymphadenopathy. Histology of a mediastinal lymph node obtained by video-assisted thoroscopic excision confirmed the diagnosis of histiocytic necrotizing lymphadenitis. To our knowledge, this is the first report of...

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