ArticleHeliyon2024
Kimura disease, a rare Ethiopian case report.
Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
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, 1 synthesis or guideline pooled it.
- A Comprehensive Review of Kimura Disease.Head and neck pathology · 2025Pooled it
- Retroauricular Kimura Disease in a Young European Female: A Rare Case and Review of the Literature.Life (Basel, Switzerland) · 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Kimura disease is a chronic inflammatory disorder predominantly affecting the head and neck region. The etiology of Kimura disease remains unclear. The disease mainly affects young adult males of Asian descent, with a higher prevalence in East Asian countries. Clinical presentation: a 48-year-old Ethiopian woman presented with swelling in both her lower extremities, which gradually progressed to include her abdomen and the rest of her body. Additionally, she had pain in multiple joints in her upper and lower extremities, high-grade fever, loss of appetite, night sweats, and unexplained weight loss over the same duration. Physical examination revealed swelling around the eyes (periorbital puffiness), enlarged nodes in the axillary, and inguinal areas on both sides of the body, and pitting edema. Investigations showed pneumonia, elevated renal function tests and kimura disease. Unfortunately, the patient signed medical advice before completing her management. Conclusion: despite its rarity in Ethiopia, it is imperative to consider Kimura disease as a potential diagnosis when evaluating lymphadenopathy and renal derangement.
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Registered trials
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