1. Kikuchi-Fujimoto disease in children: two case reports and a review of the literature
- Author
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Ilaria Amodeo, Mara Lelii, Paola Marchisio, Samantha Bosis, Laura Senatore, Raffaella Pinzani, Stefano Fiori, and Sara Torretta
- Subjects
Male ,Kikuchi-Fujimoto disease ,Pediatrics ,medicine.medical_specialty ,Adolescent ,Case Report ,Hemophagocytic lymphohistiocytosis ,03 medical and health sciences ,0302 clinical medicine ,Lymphadenitis ,Cervical lymphadenopathy ,030225 pediatrics ,medicine ,Humans ,Fever of unknown origin ,Child ,Persistent fever ,Histiocytic Necrotizing Lymphadenitis ,business.industry ,lcsh:RJ1-570 ,Respiratory infection ,lcsh:Pediatrics ,Relapsing Kikuchi-Fujimoto disease ,Recurrent lymphadenitis ,medicine.disease ,Rash ,030220 oncology & carcinogenesis ,Etiology ,Female ,Chills ,medicine.symptom ,Differential diagnosis ,business ,HLH - Abstract
Background Kikuchi-Fujimoto disease is a rare, idiopathic and generally self-limiting cause of lymphadenitis of unknow etiology with a low recurrence rate. The typical clinical signs are cervical lymphadenopathy, fever, and symptoms of respiratory infection, and less frequently chills, night sweats, arthralgia, rash, and weight loss. Case presentation Here we describe two case reports of Kikuchi Fujimoto disease presenting in Milan within the space of a few months. The first involved the recurrence of KFD in a young boy from Sri Lanka; the second was a rare case of severe KFD complicated by HLH. Conclusions Pediatricians must consider KFD in the differential diagnosis of fever of unknown origin in children, even in western countries. Although rare, recurrence and severe complications are possible. Where symptoms suggest KFD, a systematic diagnostic approach is key. Since no guidelines on the management of KFD are available, further studies should be conducted to investigate the therapeutic options and long term outcome in children.
- Published
- 2018
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