{"title":"Clinicopathological comparison and cytokeratin-10 expression between Lichen planus and oral lichenoid lesions","authors":"Milena Duarte Moreira, Luanna Canal Pereira, Tahyna Duda Deps, Tânia Regina Grão Velloso, Letícia Nogueira da Gama-de-Souza, Liliana Aparecida Pimenta-Barros, Danielle Resende Camisasca","doi":"10.1016/j.archoralbio.2024.106166","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to compare clinicopathological features and immunostaining for cytokeratin-10 between oral lichen planus and oral lichenoid lesions.</div></div><div><h3>Design</h3><div>This was a retrospective longitudinal study comparing lichen planus and oral lichenoid lesions diagnosed at the Oral Pathological Anatomy Service that analyzed sociodemographic and clinicopathological data and CK10 expression. Chi-square tests, Fisher's exact tests and Mann-Whitney tests or Student's t tests were used when appropriate, and p values < 0.05 were considered significant.</div></div><div><h3>Results</h3><div>A total of 23 lichen planus and 23 lichenoid lesions were included. There was an association between oral lichen planus and symptomatology (p = 0.031). The buccal mucosa was the most affected site in both groups: 20 patients (87.0 %) showed oral lichen planus, and 16 patients (69.6 %) oral lichenoid lesions. Bilateral (p < 0.001) striae (p = 0.004) are more characteristic of oral lichen planus. Oral lichen planus was associated with degeneration of the basal layer (p = 0.049) and with mild epithelial dysplasia (p < 0.001). Cytokeratin-10 immunostaining was similar between the groups.</div></div><div><h3>Conclusions</h3><div>A continuous follow-up is necessary to identify different patterns of malignant transformation between groups of lesions, as well as for comparisons with lesions with a higher malignant transformation rate.</div></div>","PeriodicalId":8288,"journal":{"name":"Archives of oral biology","volume":"171 ","pages":"Article 106166"},"PeriodicalIF":2.2000,"publicationDate":"2024-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of oral biology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003996924002875","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
This study aimed to compare clinicopathological features and immunostaining for cytokeratin-10 between oral lichen planus and oral lichenoid lesions.
Design
This was a retrospective longitudinal study comparing lichen planus and oral lichenoid lesions diagnosed at the Oral Pathological Anatomy Service that analyzed sociodemographic and clinicopathological data and CK10 expression. Chi-square tests, Fisher's exact tests and Mann-Whitney tests or Student's t tests were used when appropriate, and p values < 0.05 were considered significant.
Results
A total of 23 lichen planus and 23 lichenoid lesions were included. There was an association between oral lichen planus and symptomatology (p = 0.031). The buccal mucosa was the most affected site in both groups: 20 patients (87.0 %) showed oral lichen planus, and 16 patients (69.6 %) oral lichenoid lesions. Bilateral (p < 0.001) striae (p = 0.004) are more characteristic of oral lichen planus. Oral lichen planus was associated with degeneration of the basal layer (p = 0.049) and with mild epithelial dysplasia (p < 0.001). Cytokeratin-10 immunostaining was similar between the groups.
Conclusions
A continuous follow-up is necessary to identify different patterns of malignant transformation between groups of lesions, as well as for comparisons with lesions with a higher malignant transformation rate.
期刊介绍:
Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including:
Cell and molecular biology
Molecular genetics
Immunology
Pathogenesis
Cellular microbiology
Embryology
Syndromology
Forensic dentistry