ArticleCureus2025
Kimura's 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. Cited by 2 papers.
What it found
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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.
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.
Who cites it
2 citing papers in PubMed.
- Inguinal kimura disease misdiagnosed as Castleman disease: A case report and analysis of ultrasonographic features.Radiology case reports · 2026Article
- Kimura disease presenting as a right lower limb soft tissue tumor: a case report.Frontiers in medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Kimura's disease (KD) is a rare, chronic, autoinflammatory condition of unknown etiology, typically involving lymphoid and/or extranodal tissues of the head and neck area, usually presenting with peripheral blood eosinophilia and elevated serum immunoglobulin E (IgE) levels. The clinical features of KD are often variable and nonspecific, overlapping with other hematologic conditions, leading to diagnostic challenges. We report a case of a 36-year-old female with no prior medical history who presented with bilateral cervical lymphadenopathy, nodular lesions in the scalp, and elevated IgE levels, diagnosed with KD. We present a scoping review of the literature focusing on mass-like presentations of the head and neck region, recording the demographics, the clinical manifestation, the histopathology, and imaging findings, as well as the treatment and the outcomes. This case report and literature review highlight the necessity of clinical awareness of this rare condition and emphasize the need for interdisciplinary collaboration in the diagnostic process.
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Registered trials
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.