ArticleCureus2025
Kikuchi Disease in a Young Woman With Sickle Cell Disease: A Case Report.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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Abstract
Kikuchi-Fujimoto disease (KFD) is a rare, benign, and self-limiting disorder characterized by necrotizing lymphadenitis, primarily affecting young adults and adolescents. Its etiology and pathogenesis remain unclear and complex. Common presentations include constitutional symptoms such as lymphadenopathy and fever. This study reports the case of a 15-year-old girl who presented with a fever of unknown origin and was found to have lymphadenopathy, which was associated with sickle cell disease (SCD). The diagnosis was confirmed through the pathological features of lymph node biopsy, with the patient successfully treated with steroids and hydroxychloroquine. She remained stable on follow-up, with no recurrence of fever or lymphadenopathy.
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