Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica

Detalhes bibliográficos
Autor(a) principal: Pereira, Luanna Canal
Data de Publicação: 2023
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
Texto Completo: http://repositorio.ufes.br/handle/10/12673
Resumo: Introduction: Oral potentially malignant disorders (OPMDs) are a group of oral lesions associated with a variable risk of progression to oral carcinomas. Oral leukoplakia (OL) is the most common OPMD. Proliferative verrucous leukoplakia (PVL) is a subtype of OL with a high risk of progression to carcinoma. Cytokeratin 10 (CK10) acts to differentiate normal from dysplastic epithelium. Objectives: Compare sociodemographic, clinical, histopathological and immunohistochemical characteristics of CK10 in OL and PVL and apply two diagnostic criteria for PVL. Materials and methods: Cases diagnosed as OL, PVL, epithelial dysplasia and hyperkeratosis without and with dysplasia were selected from the Oral Pathological Anatomy Service of the Federal University of Espírito Santo, in ten years. Sociodemographic, clinicopathological and immunohistochemical data were collected. A p-value ≤.05 was considered was considered statistically significant. Results: 51 patients (n=32, 62.7% LVP and n=19, 37.3% LO) and 104 lesions (n=76, 73% LVP and n=28, 26.9% LO) were selected, with 53 lesions submitted to immunohistochemical staining for CK10 (n=40, 75.4% LVP and n=13, 24.5% LO), with a mean follow-up of 13 months for LO and 27 months for LVP (p=0.038). There was a predominance of females in both, an association between tobacco use and LO (p= 0.007) and the presence of recurrence in PVL lesions (p=0.028). There was malignant transformation in two cases of PVL and one of LO. Almost all lesions were positive for CK10 (n=51, 96.3%). No lesion showed CK10 expression in the basal layer. When applying the criteria for PVL, all met the criteria of Cerero-Lapiedra et al., 2010 and 19 patients met the criteria of Villa et al., 2018. Conclusions: Tobacco use is associated with LO, but not with LVP. The two criteria applied were useful, CereroLapiedra et al., 2010 selects more patients, a favorable fact for better monitoring of the disease. There was no difference in CK10 expression between the lesions studied.
id UFES_7c322a42d2a3a2eb427168797c4542fd
oai_identifier_str oai:repositorio.ufes.br:10/12673
network_acronym_str UFES
network_name_str Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
repository_id_str 2108
spelling Barroso, Danielle Resende Camisascahttp://lattes.cnpq.br/3989074593181674Pereira, Luanna Canalhttps://orcid.org/0000-0001-9582-7067http://lattes.cnpq.br/8124717525751212Lourenço, Simone de Queiroz ChavesBarros, Liliana Aparecida Pimenta dehttp://lattes.cnpq.br/86352776600808402024-05-29T20:55:39Z2024-05-29T20:55:39Z2023-12-18Introduction: Oral potentially malignant disorders (OPMDs) are a group of oral lesions associated with a variable risk of progression to oral carcinomas. Oral leukoplakia (OL) is the most common OPMD. Proliferative verrucous leukoplakia (PVL) is a subtype of OL with a high risk of progression to carcinoma. Cytokeratin 10 (CK10) acts to differentiate normal from dysplastic epithelium. Objectives: Compare sociodemographic, clinical, histopathological and immunohistochemical characteristics of CK10 in OL and PVL and apply two diagnostic criteria for PVL. Materials and methods: Cases diagnosed as OL, PVL, epithelial dysplasia and hyperkeratosis without and with dysplasia were selected from the Oral Pathological Anatomy Service of the Federal University of Espírito Santo, in ten years. Sociodemographic, clinicopathological and immunohistochemical data were collected. A p-value ≤.05 was considered was considered statistically significant. Results: 51 patients (n=32, 62.7% LVP and n=19, 37.3% LO) and 104 lesions (n=76, 73% LVP and n=28, 26.9% LO) were selected, with 53 lesions submitted to immunohistochemical staining for CK10 (n=40, 75.4% LVP and n=13, 24.5% LO), with a mean follow-up of 13 months for LO and 27 months for LVP (p=0.038). There was a predominance of females in both, an association between tobacco use and LO (p= 0.007) and the presence of recurrence in PVL lesions (p=0.028). There was malignant transformation in two cases of PVL and one of LO. Almost all lesions were positive for CK10 (n=51, 96.3%). No lesion showed CK10 expression in the basal layer. When applying the criteria for PVL, all met the criteria of Cerero-Lapiedra et al., 2010 and 19 patients met the criteria of Villa et al., 2018. Conclusions: Tobacco use is associated with LO, but not with LVP. The two criteria applied were useful, CereroLapiedra et al., 2010 selects more patients, a favorable fact for better monitoring of the disease. There was no difference in CK10 expression between the lesions studied.Introdução: As desordens orais com potencial de malignização (DOPMs) são um grupo lesões orais associadas a risco variável de progressão para carcinoma oral. A leucoplasia oral (LO) é a DOPM mais comum. A leucoplasia verrucosa proliferativa (LVP) é um subtipo da LO com alto risco de progressão para carcinoma. A citoqueratina 10 (CK10) atua para diferenciar epitélio normal do displásico. Objetivos: Comparar características sociodemográficas, clínicas, histopatológicas e imunohistoquímicas da CK10 na LO e na LVP e aplicar dois critérios diagnósticos para LVP. Materiais e métodos: Foram selecionados casos diagnosticados como LO, LVP, displasia epitelial e hiperceratose sem e com displasia, do Serviço de Anatomia Patológica Bucal da Universidade Federal do Espírito Santo, em dez anos. Os dados sociodemográficos, clínicopatológicos e imunohistoquímicos foram coletados. Foi considerado significativo p-valor <0,05. Resultados: Foram selecionados 51 pacientes (n=32, 62,7% LVP e n=19, 37,3% LO) e 104 lesões (n=76, 73% LVP e n=28, 26,9% LO), sendo 53 lesões submetidas à marcação imunohistoquímica para CK10 (n=40, 75,4% LVP e n=13, 24,5% LO), com o tempo médio de acompanhamento de 13 meses para LO e 27 meses para LVP (p=0,038). Houve predomínio do gênero feminino em ambas, associação entre uso de tabaco e LO (p= 0,007) e presença de recidiva em lesões de LVP (p=0,028). Houve transformação maligna em dois casos de LVP e um de LO. Quase todas as lesões foram positivas para CK10 (n=51, 96,3%). Nenhuma lesão apresentou expressão da CK10 em camada basal. Ao aplicar os critérios para LVP, todos preencheram os critérios de Cerero-Lapiedra et al., 2010 e 19 pacientes preencheram os critérios de Villa et al., 2018. Conclusões: O uso de tabaco está associado a LO, porém não à LVP. Os dois critérios aplicados foram úteis, Cerero-Lapiedra et al., 2010 seleciona mais pacientes, fato favorável para melhor acompanhamento da doença. Não houve diferença na expressão da CK10 entre as lesões estudadas.Fundação de Amparo à Pesquisa do Espírito Santo (FAPES)Texthttp://repositorio.ufes.br/handle/10/12673porUniversidade Federal do Espírito SantoMestrado em Ciências OdontológicasPrograma de Pós-Graduação em Ciências OdontológicasUFESBRCentro de Ciências da SaúdeCiências da SaúdeLeucoplasia oralCarcinoma de células escamosasCitoqueratinaLeucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímicainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)instname:Universidade Federal do Espírito Santo (UFES)instacron:UFESORIGINALLuannaCanalPereira-2023-Trabalho.pdfapplication/pdf1052108http://repositorio.ufes.br/bitstreams/2288cd6e-41ad-4ae3-894e-eaab59d7183a/download7424551e96fb8d815ebe25125554c26fMD5110/126732024-09-18 09:37:55.434oai:repositorio.ufes.br:10/12673http://repositorio.ufes.brRepositório InstitucionalPUBhttp://repositorio.ufes.br/oai/requestopendoar:21082024-10-15T17:57:11.890680Repositório Institucional da Universidade Federal do Espírito Santo (riUfes) - Universidade Federal do Espírito Santo (UFES)false
dc.title.none.fl_str_mv Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
title Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
spellingShingle Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
Pereira, Luanna Canal
Ciências da Saúde
Leucoplasia oral
Carcinoma de células escamosas
Citoqueratina
title_short Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
title_full Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
title_fullStr Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
title_full_unstemmed Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
title_sort Leucoplasia oral e leucoplasia verrucosa proliferativa: análise clínico-patológica e imunohistoquímica
author Pereira, Luanna Canal
author_facet Pereira, Luanna Canal
author_role author
dc.contributor.authorID.none.fl_str_mv https://orcid.org/0000-0001-9582-7067
dc.contributor.authorLattes.none.fl_str_mv http://lattes.cnpq.br/8124717525751212
dc.contributor.advisor1.fl_str_mv Barroso, Danielle Resende Camisasca
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/3989074593181674
dc.contributor.author.fl_str_mv Pereira, Luanna Canal
dc.contributor.referee1.fl_str_mv Lourenço, Simone de Queiroz Chaves
dc.contributor.referee2.fl_str_mv Barros, Liliana Aparecida Pimenta de
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/8635277660080840
contributor_str_mv Barroso, Danielle Resende Camisasca
Lourenço, Simone de Queiroz Chaves
Barros, Liliana Aparecida Pimenta de
dc.subject.cnpq.fl_str_mv Ciências da Saúde
topic Ciências da Saúde
Leucoplasia oral
Carcinoma de células escamosas
Citoqueratina
dc.subject.por.fl_str_mv Leucoplasia oral
Carcinoma de células escamosas
Citoqueratina
description Introduction: Oral potentially malignant disorders (OPMDs) are a group of oral lesions associated with a variable risk of progression to oral carcinomas. Oral leukoplakia (OL) is the most common OPMD. Proliferative verrucous leukoplakia (PVL) is a subtype of OL with a high risk of progression to carcinoma. Cytokeratin 10 (CK10) acts to differentiate normal from dysplastic epithelium. Objectives: Compare sociodemographic, clinical, histopathological and immunohistochemical characteristics of CK10 in OL and PVL and apply two diagnostic criteria for PVL. Materials and methods: Cases diagnosed as OL, PVL, epithelial dysplasia and hyperkeratosis without and with dysplasia were selected from the Oral Pathological Anatomy Service of the Federal University of Espírito Santo, in ten years. Sociodemographic, clinicopathological and immunohistochemical data were collected. A p-value ≤.05 was considered was considered statistically significant. Results: 51 patients (n=32, 62.7% LVP and n=19, 37.3% LO) and 104 lesions (n=76, 73% LVP and n=28, 26.9% LO) were selected, with 53 lesions submitted to immunohistochemical staining for CK10 (n=40, 75.4% LVP and n=13, 24.5% LO), with a mean follow-up of 13 months for LO and 27 months for LVP (p=0.038). There was a predominance of females in both, an association between tobacco use and LO (p= 0.007) and the presence of recurrence in PVL lesions (p=0.028). There was malignant transformation in two cases of PVL and one of LO. Almost all lesions were positive for CK10 (n=51, 96.3%). No lesion showed CK10 expression in the basal layer. When applying the criteria for PVL, all met the criteria of Cerero-Lapiedra et al., 2010 and 19 patients met the criteria of Villa et al., 2018. Conclusions: Tobacco use is associated with LO, but not with LVP. The two criteria applied were useful, CereroLapiedra et al., 2010 selects more patients, a favorable fact for better monitoring of the disease. There was no difference in CK10 expression between the lesions studied.
publishDate 2023
dc.date.issued.fl_str_mv 2023-12-18
dc.date.accessioned.fl_str_mv 2024-05-29T20:55:39Z
dc.date.available.fl_str_mv 2024-05-29T20:55:39Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufes.br/handle/10/12673
url http://repositorio.ufes.br/handle/10/12673
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv Text
dc.publisher.none.fl_str_mv Universidade Federal do Espírito Santo
Mestrado em Ciências Odontológicas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Ciências Odontológicas
dc.publisher.initials.fl_str_mv UFES
dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal do Espírito Santo
Mestrado em Ciências Odontológicas
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
instname:Universidade Federal do Espírito Santo (UFES)
instacron:UFES
instname_str Universidade Federal do Espírito Santo (UFES)
instacron_str UFES
institution UFES
reponame_str Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
collection Repositório Institucional da Universidade Federal do Espírito Santo (riUfes)
bitstream.url.fl_str_mv http://repositorio.ufes.br/bitstreams/2288cd6e-41ad-4ae3-894e-eaab59d7183a/download
bitstream.checksum.fl_str_mv 7424551e96fb8d815ebe25125554c26f
bitstream.checksumAlgorithm.fl_str_mv MD5
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Espírito Santo (riUfes) - Universidade Federal do Espírito Santo (UFES)
repository.mail.fl_str_mv
_version_ 1813022540716572672