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Diagnosis of Kikuchi-Fujimoto disease in an 11-year-old girl with fever and sickle cell disease.
Cannon, Laura; Wang, Endi; Becker, Mara.
Affiliation
  • Cannon L; Division of Pediatric Rheumatology, Department of Pediatrics, Duke Children's Hospital and Health Center, Durham, North Carolina, USA LauraACannon86@gmail.com.
  • Wang E; Department of Pathology, Duke University Hospital, Durham, North Carolina, USA.
  • Becker M; Division of Pediatric Rheumatology, Department of Pediatrics, Duke Children's Hospital and Health Center, Durham, North Carolina, USA.
BMJ Case Rep ; 13(8)2020 Aug 24.
Article in En | MEDLINE | ID: mdl-32843398
Kikuchi-Fujimoto disease (KFD) is a rare lymphohistiocytic disorder which can cause prolonged fever and other systemic B symptoms including diffuse lymphadenopathy. Given its clinical presentation, there is often initial concern for lymphoma and diagnosis requires lymph node biopsy. It most frequently affects young women of Asian descent; it is less commonly encountered in paediatric patients. KFD is typically a benign, self-limited process, however, there is an association with development of systemic lupus erythematosus. Given its rarity, it remains unclear if KFD is associated with other chronic conditions. Here we present the third case of KFD occurring in a paediatric patient with sickle cell disease.
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Full text: 1 Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Fever / Anemia, Sickle Cell Type of study: Diagnostic_studies / Etiology_studies Limits: Child / Female / Humans Language: En Journal: BMJ Case Rep Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Fever / Anemia, Sickle Cell Type of study: Diagnostic_studies / Etiology_studies Limits: Child / Female / Humans Language: En Journal: BMJ Case Rep Year: 2020 Type: Article Affiliation country: United States