نتایج جستجو برای: kikuchi disease

تعداد نتایج: 1490654  

Journal: :The Israel Medical Association journal : IMAJ 2010
Hadar Duskin-Bitan Shaye Kivity David Olchovsky Ginette Schiby David Ezra Meir Mouallem

BACKGROUND Kikuchi-Fujimoto disease is a benign and self-limited disease, first reported in Japan in 1972. The characteristic features of this disorder include lymphadenopathy and fever. OBJECTIVES To summarize our experience with Kikuchi disease with regard to clinical manifestations and outcome. METHODS The patients included in the study were those diagnosed with Kikuchi disease during th...

2009
David J. Archibald Matthew L. Carlson Ray O. Gustafson

Kikuchi-Fujimoto disease is a rare, self-limited, histiocytic, necrotizing lymphadenitis first described in Japan in 1972. Necrosis of lymph node tissue is caused by apoptosis and may be virally induced. It commonly presents with cervical lymphadenitis and fever. Despite its low incidence, Kikuchi-Fujimoto disease should be considered in patients with persistent lymphadenopathy. Originally thou...

2012
Juan Garcia-Arnes M Rosa Bernal-Lopez Jose Luis Gallego-Perales M Luz Vazquez-Camuñas Ricardo Gomez-Huelgas

UNLABELLED INTRODUCTION Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a rare, benign, autoimmune condition characterized by lymphadenopathy, fever and neutropenia. It is a self-limited condition of unknown etiology. CASE PRESENTATION We report the case of a 45-year-old Caucasian man with the first known case of Kikuchi disease associated with dramatic weight loss a...

Journal: :BMJ case reports 2014
John Ming Ren Loh Humaira Shafi

We present a case report of a 41-year-old woman of Malay ethnicity who presented with an 11-day history of fever and left-sided lymphadenopathy after consuming 'Miracle Mineral Solution' (sodium chlorite solution) for the first time. A diagnosis of Kikuchi-Fujimoto disease was established via lymph node biopsy after other differentials were excluded. The aetiology of Kikuchi-Fujimoto disease re...

2017
Chamara Dalugama Indika Bandara Gawarammana

BACKGROUND Kikuchi Fujimoto disease is an uncommon benign condition of necrotizing histiocytic lymphadenitis commonly seen in East Asian and Japanese populations. It commonly presents with fever, cervical lymphadenopathy, and elevated inflammatory markers. Diagnosis of Kikuchi Fujimoto disease is based on histopathological studies of the involved lymph nodes. The presentation of Kikuchi Fujimot...

Journal: :American Journal of Clinical Pathology 2004

Journal: :The Medical journal of Malaysia 2002
R Bachi

A 27-year old woman presented with fever, weight loss, arthralgia, macular skin rash and bilateral axillary lymphadenopathy. The histology of an excised lymph node showed evidence suggestive of Kikuchi disease. Subsequent laboratory tests showed evidence of Systemic Lupus Erythematosus, underscoring the importance of considering other diagnoses in a nodal histological diagnosis of Kikuchi disea...

2015
Inseon Ryoo Sangil Suh Young Hen Lee Hyung Suk Seo Hae Young Seol

OBJECTIVE Although tuberculous lymphadenitis and Kikuchi disease are common causes of cervical lymphadenopathy in Asians and exhibit similar clinical manifestations, their treatment strategies are totally different. The purpose of this study was to identify ultrasonographic features that distinguish these two diseases. MATERIALS AND METHODS This study was approved by the Institutional Review ...

2017
Hidenori Kido Osamu Kano Asami Hamai Hiroyuki Masuda Yutaka Fuchinoue Masaaki Nemoto Chiaki Arai Teppei Takeda Fumihito Yamabe Toshihiro Tai Mizuki Kasahara Kenichi Suzuki Nobuyuki Shiraga Sota Sadamoto Megumi Wakayama Yukitoshi Takahashi Yasuo Iwasaki Kazutoshi Shibuya Yoshihisa Urita

BACKGROUND Kikuchi-Fujimoto disease is a self-limited clinicopathologic entity that is increasingly recognized worldwide. Kikuchi-Fujimoto disease is characterized by cervical lymphadenopathy occurring in young adults. Neurologic involvement is rare, and testitis directly caused by Kikuchi-Fujimoto disease has not yet been reported. CASE PRESENTATION A 19-year-old man was brought to our clini...

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