ArticleFrontiers in pediatrics2023
Kimura disease in children: A report of 11 cases and review of the literature.
Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 18 citations in OpenAlex.
- Kimura Disease Presenting as Cervical Lymphadenopathy with Marked Eosinophilia in a Saudi Adolescent: A Case Report and Literature Review.Healthcare (Basel, Switzerland) · 2026Article
- Long-term clinical course and recurrence pattern of orbital Kimura's disease: a retrospective case series.BMC ophthalmology · 2026Article
- Two Pediatric Cases of Kimura Disease Following Vaccination.Yonago acta medica · 2026Article
- Pruritic Plaque on the Right Lower Limb: A Rare Case of Kimura Disease and Literature Review.Clinical case reports · 2025Article
- Kimura's Disease: A Case Report.Cureus · 2025Article
- FSGS in Kimura Disease - A Rare Cause of Nephrotic Syndrome in an Adolescent.Indian journal of pediatrics · 2025Article
- Article
- Kimura Disease: A Detailed Analysis of Clinical and Radiological Manifestations in a Retrospective Case Series.Journal of inflammation research · 2024Article
- The clinical and pathological features of Kimura disease in pediatric patients.Frontiers in medicine · 2024Article
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Kimura disease (KD), also known as eosinophilic hyperplastic lymphoid granuloma, is a rare benign chronic inflammatory condition, which is featured with the painless progressive mass located in the subcutaneous area of the head and neck region, elevated peripheral blood eosinophils, and raised serum immunoglobulin E (IgE) levels. KD is uncommon in clinical practice, especially with low incidence in children, so it often leads to misdiagnosis or missed diagnosis in pediatric patients. Methods: The clinical data of 11 pediatric patients with KD in the authors' institution were retrospectively analyzed. Results: There were 11 pediatric patients with KD enrolled in total, including 9 male patients and 2 female patients (sex ratio 4.5:1). The median age at diagnosis stood at 14 years (range 5-18 years), the initial symptoms in all patients included painless subcutaneous masses and focal swelling, the duration of symptoms ranged from 1 month to 10 years, and the average duration was 24.45 months. Six patients had single lesions, and 5 had multiple lesions. The highest proportion of lesion regions were parotid gland ( Conclusion: Base on the study, it is found that Kimura disease is rare and may have the atypical symptoms in pediatric patients, combination therapy is recommended to reduce recurrence, and long-term follow-up should be performed.
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