Evidence map›Paper›PMID 41409906›Full record

ArticleCureus2025

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

Robert Baxter, Corinne Russell, Katharine Benedict

Abstract readCase Reports
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Robert BaxterInternal Medicine, Lister Hospital, Stevenage, GBR.
Corinne RussellInternal Medicine, Lister Hospital, Stevenage, GBR.
Katharine BenedictInternal Medicine, Lister Hospital, Stevenage, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

autoimmunedifferential diagnosiskikuchi-fujimoto diseaselymphomanecrotizing lymphadenitis

Identifiers

PMID41409906
PMCPMC12706627

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.