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A Rare Differential for Myalgia and Fever Associated With Cervical and Axillary Lymphadenopathy Presenting via Same Day Emergency Care.

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Cureus 📖 저널 OA 99.9% 2021: 42/43 OA 2022: 79/79 OA 2023: 181/181 OA 2024: 284/284 OA 2025: 774/774 OA 2026: 506/506 OA 2021~2026 2025 Vol.17(11) p. e96947
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Baxter R, Russell C, Benedict K

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Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting necrotising lymphadenitis, mainly affecting young adults, and commonly presenting with fevers and lymphadenopathy.

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APA Baxter R, Russell C, Benedict K (2025). A Rare Differential for Myalgia and Fever Associated With Cervical and Axillary Lymphadenopathy Presenting via Same Day Emergency Care.. Cureus, 17(11), e96947. https://doi.org/10.7759/cureus.96947
MLA Baxter R, et al.. "A Rare Differential for Myalgia and Fever Associated With Cervical and Axillary Lymphadenopathy Presenting via Same Day Emergency Care.." Cureus, vol. 17, no. 11, 2025, pp. e96947.
PMID 41409906 ↗

Abstract

Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting necrotising lymphadenitis, mainly affecting young adults, and commonly presenting with fevers and lymphadenopathy. Diagnosis is confirmed by histopathological examination via lymph node biopsy, and management is primarily supportive with non-steroidal anti-inflammatory drugs and/or a tapering course of steroids. We herein describe a case of a 23-year-old Caucasian female with severe KFD. She presented to the same day emergency care (SDEC) with a six-week history of systemic symptoms, including myalgia, arthralgia, fevers, and weight loss. Her initial blood tests showed normocytic anaemia, leukopenia, abnormal liver function tests, and a raised erythrocyte sedimentation rate. Notable aspects of this case include the large range of presenting symptoms, a coexisting Epstein-Barr virus (EBV) infection, and a delay in diagnosis of 14 days with a long inpatient admission. KFD poses a diagnostic dilemma due to its non-specific presentation, with differentials from a range of varying aetiologies, including infective (EBV), rheumatological (systemic lupus erythematosus (SLE), adult Still's disease), haematological (lymphoma), and others (sarcoidosis, tuberculosis). For our patient, the early working diagnoses of SLE and lymphoma prompted consideration of a transfer to a specialist haematology oncology bed. This case highlights the importance of early histopathological diagnoses in KFD and the need for a multidisciplinary approach, including haematology colleagues, commenced early in the acute setting to avoid misdiagnoses and unnecessary anxiety for patients. Currently, no specific national guidelines exist for KFD, and management is focused on supportive care. By sharing our experience, we hope to increase awareness of KFD's clinical presentation, diagnosis, and management amongst clinicians to avoid diagnostic delay or unnecessary interventions and guide timely therapeutic decisions.

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