Kikuchi-Fujimoto Disease: A Sinister Morphology Having a Benign Course
نویسندگان
چکیده
منابع مشابه
Kikuchi-Fujimoto disease* Doença de Kikuchi-Fujimoto
Kikuchi-Fujimoto disease is characterized by fever and lymphadenopathy, usually localized in the cervical region. This disease principally affects young females. It can be confused with lymphoma, adenocarcinoma metastasis and tuberculosis. We report two cases of KikuchiFujimoto disease. In the first case, a 28-year-old female had been treated for tuberculosis one year prior and presented with a...
متن کاملKikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis
Kikuchi-Fujimoto disease (KFD) is a benign, self-limiting disease characterized by histiocytic necrotising lymphadenitis. Though several viral agents or an autoimmune etiology has been proposed as causative, the exact cause remains unknown. It has a female predilection and most commonly seen among young Asian people. Patients usually present with a febrile illness and the presence of lymphadeno...
متن کاملKikuchi-Fujimoto disease.
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...
متن کاملKikuchi-Fujimoto disease in children: clinical features and disease course.
Kikuchi-Fujimoto disease (KFD) is a rare cause of cervical lymphadenitis which mostly affects Asian women but is sometimes observed in the pediatric population. This study analyzed the clinical manifestations and disease course in children with KFD. Retrospective chart review and telephone interview were used to collect data for 13 children (8 boys and 5 girls) with a diagnosis of KFD from Janu...
متن کاملFamilial Kikuchi-Fujimoto disease
Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting disease of unknown aetiology presenting with cervical lymphadenopathy, fever, vomiting, weight loss, night sweats and chills. Familial occurrence of KFD is reported very rarely in literature. We report two cases from the same family presenting with KFD. The two non-twin sisters presented with symptoms of fever, cervical lymphadenopathy, we...
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ژورنال
عنوان ژورنال: Journal of Case Reports
سال: 2016
ISSN: 2231-6809
DOI: 10.17659/01.2016.0121