ArticleCase reports in dentistry2026
Multifocal Epithelial Hyperplasia: Persistence in Adulthood and Treatment-A Case Report.
Article in Case reports in dentistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Multifocal Epithelial Hyperplasia: Persistence in Adulthood and Treatment-A Case Report.Case reports in dentistry · 2026Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Multifocal epithelial hyperplasia (MEH) is a rare, benign epithelial pathology associated with the human papillomavirus (HPV) infection, affecting the oral mucosa. It is primarily observed in children, particularly those from indigenous populations of Latin American origin and typically resolves during adolescence. However, this case report presents a patient with persistent lesions into adulthood. Despite pharmacological treatment, no significant improvements were observed. Case Report: A 55-year-old female patient of indigenous descent presented with multiple asymptomatic papillomatous lesions of varying sizes, which had been present since the age of 12. There were no systemic comorbidities. The presence of multiple lesions and the patient's age, differential diagnoses such as Cowden syndrome and oral papillomatosis were considered and subsequently ruled out following clinical evaluation. Histopathological analysis confirmed the initial findings, establishing a definite diagnosis of MEH. The patient underwent combined surgical and pharmacological treatment, involving the application of 80% trichloroacetic acid and 5% imiquimod. Conclusion: Few case reports of MEH in adult patients exist, and none have thoroughly evaluated the effectiveness of pharmacological treatments. This case underscores the inconsistency of pharmacological therapies in adults, as most studies have focused predominantly on pediatric populations. Therefore, further investigation into alternative pharmacological approaches is warranted for the management of MEH in adult patients.
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