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1.
Oral Dis ; 28(8): 2072-2082, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34333825

RESUMO

To integrate the available data published on malignant peripheral nerve sheath tumours (MPNST) of the oral and maxillofacial region. Searches in Embase, PubMed, Web of Science and Scopus were conducted for the identification of case reports/case series in English language. The risk of bias was assessed using the Joanna Briggs Institute tool. Outcomes were evaluated by Cox regression and Kaplan-Meier methods. A total of 306 articles were retrieved, 50 of which reporting 57 MPNST were included. The lesion showed a predilection for the mandible (n = 18/31.57%) of middle-aged adults (~40.5 years) with a male/female ratio of 1.1:1. The individuals were mostly symptomatic with a mean evolution time of 9.6 months. Surgical removal plus adjuvant therapy (especially radiotherapy) was the main approach (51.86%). Recurrence was reported in 39.62% of cases. Nodal and distant metastases were identified in 28.26% and 26.66% of cases, respectively. The 2-year cumulative survival rate was 55%. Independent predictors of poor survival were the presence of neurofibromatosis type 1 (p = 0.04) and distant metastases (p = 0.004). The diagnosis of MPNST is challenging due to the variety of its clinical and histopathological presentations. Local aggressiveness and the potential for metastases are common outcomes of this neoplasm.


Assuntos
Neoplasias Bucais , Neoplasias de Bainha Neural , Neurofibromatose 1 , Neurofibrossarcoma , Adulto , Terapia Combinada , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Recidiva Local de Neoplasia , Neoplasias de Bainha Neural/diagnóstico , Neoplasias de Bainha Neural/patologia , Neoplasias de Bainha Neural/cirurgia , Neurofibromatose 1/diagnóstico , Neurofibromatose 1/patologia , Neurofibromatose 1/terapia
2.
J Dev Orig Health Dis ; 11(5): 521-532, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32631472

RESUMO

The Developmental Origins of Health and Disease (DOHaD) states that intrauterine maternal environment influences postnatal life by programming offspring's metabolism. Intrauterine milieu induced by exercise during pregnancy promotes long-lasting benefits to the offspring's health and seems to offer some resistance against chronic diseases in adult life. Alzheimer's disease is a public health concern with limited treatment options. In the present study, we assessed the potential of maternal exercise during pregnancy in long-term programming of young adult male rat offspring's cerebellar metabolism in conferring neuroprotection against amyloid-ß (Aß) neurotoxicity. Female Wistar rats were submitted to a swimming protocol 1 week prior mating and throughout pregnancy (five sessions/a week lasting 30 min). Aß oligomers were infused bilaterally in the brain ventricles of 60-day-old male offspring. Fourteen days after surgery, we measured parameters related to redox state, mitochondrial function, and the immunocontent of proteins related to synaptic function. We found that maternal exercise during pregnancy attenuated several parameters in the offspring's male rat cerebellum, such as the reactive species rise, the increase of inducible nitric oxide synthase immunocontent and tau phosphorylation induced by Aß oligomers, increased mitochondrial fission indicated by dynamin-related protein 1 (DRP1), and protein oxidation identified by carbonylation. Strikingly, we find that maternal exercise promotes changes in the rat offspring's cerebellum that are still evident in young adult life. These favorable neurochemical changes in offspring's cerebellum induced by maternal exercise may contribute to a protective phenotype against Aß-induced neurotoxicity in young adult male rat offspring.


Assuntos
Peptídeos beta-Amiloides/metabolismo , Cerebelo/patologia , Condicionamento Físico Animal/fisiologia , Efeitos Tardios da Exposição Pré-Natal/prevenção & controle , Animais , Cerebelo/metabolismo , Modelos Animais de Doenças , Feminino , Humanos , Masculino , Oxirredução , Gravidez , Efeitos Tardios da Exposição Pré-Natal/metabolismo , Efeitos Tardios da Exposição Pré-Natal/patologia , Ratos , Ratos Wistar
3.
J Appl Oral Sci ; 28: e20190532, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32348447

RESUMO

Oral leukoplakia (OL) is a white lesion of an indeterminate risk not related to any excluded (other) known diseases or disorders that carry no increased risk for cancer. Many biological markers have been used in an attempt to predict malignant transformation; however, no reliable markers have been established so far. Objective To evaluate cell proliferation and immortalization in OL, comparing non-dysplastic (Non-dys OL) and dysplastic OL (Dys OL). Methodology This is a cross-sectional observational study. Paraffin-embedded tissue blocks of 28 specimens of Non-dys OL, 33 of Dys OL, 9 of normal oral mucosa (NOM), 17 of inflammatory hyperplasia (IH), and 19 of oral squamous cell carcinomas (OSCC) were stained for Ki-67 and BMI-1 using immunohistochemistry. Results A gradual increase in BMI-1 and K-i67 expression was found in oral carcinogenesis. The immunolabeling for those markers was higher in OSCC when compared with the other groups (Kruskal-Wallis, p<0.05). Ki-67 expression percentage was higher in OL and in IH when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). Increased expression of BMI-1 was also observed in OL when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). No differences were observed in expression of both markers when non-dysplastic and dysplastic leukoplakias were compared. A significant positive correlation between Ki-67 and BMI-1 was found (Spearman correlation coefficient, R=0.26, p=0.01). High-grade epithelial dysplasia was associated with malignant transformation (Chi-squared, p=0.03). Conclusions These findings indicate that BMI-1 expression increases in early oral carcinogenesis and is possibly associated with the occurrence of dysplastic changes. Furthermore, our findings indicate that both Ki-67 and BMI-1 are directly correlated and play a role in initiation and progression of OSCC.


Assuntos
Carcinoma de Células Escamosas/patologia , Leucoplasia Oral/patologia , Neoplasias Bucais/patologia , Complexo Repressor Polycomb 1/análise , Adulto , Idoso , Análise de Variância , Carcinogênese/patologia , Estudos de Casos e Controles , Proliferação de Células , Estudos Transversais , Progressão da Doença , Feminino , Humanos , Imuno-Histoquímica , Antígeno Ki-67/análise , Masculino , Pessoa de Meia-Idade , Mucosa Bucal/patologia , Valores de Referência , Fatores de Risco , Estatísticas não Paramétricas , Carga Tumoral
4.
J. appl. oral sci ; 28: e20190532, 2020. tab, graf
Artigo em Inglês | BBO - Odontologia, LILACS | ID: biblio-1101257

RESUMO

Abstract Oral leukoplakia (OL) is a white lesion of an indeterminate risk not related to any excluded (other) known diseases or disorders that carry no increased risk for cancer. Many biological markers have been used in an attempt to predict malignant transformation; however, no reliable markers have been established so far. Objective To evaluate cell proliferation and immortalization in OL, comparing non-dysplastic (Non-dys OL) and dysplastic OL (Dys OL). Methodology This is a cross-sectional observational study. Paraffin-embedded tissue blocks of 28 specimens of Non-dys OL, 33 of Dys OL, 9 of normal oral mucosa (NOM), 17 of inflammatory hyperplasia (IH), and 19 of oral squamous cell carcinomas (OSCC) were stained for Ki-67 and BMI-1 using immunohistochemistry. Results A gradual increase in BMI-1 and K-i67 expression was found in oral carcinogenesis. The immunolabeling for those markers was higher in OSCC when compared with the other groups (Kruskal-Wallis, p<0.05). Ki-67 expression percentage was higher in OL and in IH when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). Increased expression of BMI-1 was also observed in OL when compared with NOM (Kruskal-Wallis/Dunn, p<0.05). No differences were observed in expression of both markers when non-dysplastic and dysplastic leukoplakias were compared. A significant positive correlation between Ki-67 and BMI-1 was found (Spearman correlation coefficient, R=0.26, p=0.01). High-grade epithelial dysplasia was associated with malignant transformation (Chi-squared, p=0.03). Conclusions These findings indicate that BMI-1 expression increases in early oral carcinogenesis and is possibly associated with the occurrence of dysplastic changes. Furthermore, our findings indicate that both Ki-67 and BMI-1 are directly correlated and play a role in initiation and progression of OSCC.


Assuntos
Humanos , Animais , Masculino , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Leucoplasia Oral/patologia , Neoplasias Bucais/patologia , Carcinoma de Células Escamosas/patologia , Antígeno Ki-67/análise , Complexo Repressor Polycomb 1/análise , Mucosa Bucal/patologia , Imuno-Histoquímica , Estudos Transversais , Fatores de Risco , Estatísticas não Paramétricas , Progressão da Doença , Proliferação de Células , Carcinogênese/patologia
5.
Braz Dent J ; 28(5): 543-547, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29215676

RESUMO

The aim of this study is to evaluate the immunohistochemical expression of E-cadherin, N-cadherin and Bmi-1, and their association with clinical parameters and with the degree of histopathological differentiation in oral squamous cell carcinomas. 65 squamous cell carcinoma samples were used for constructing a tissue microarray block, and then immunohistochemistry was performed for different markers. A semi-quantitative analysis of the amount of positive tumor cells was performed by two blind and calibrated observers (Kappa>0.75). The statistical Mann-Whitney and Kruskal-Wallis tests were used to evaluate the data. The correlation between variables was investigated by the Spearman test, and the significance level set at p<0.05. We observed higher expression of Bmi-1 in tumors located in the palate (p<0.0001). In addition, poorly differentiated tumors had a greater amount of Bmi-1 positive cells (p=0.0011). Regarding the other correlations between variables, no significant associations were detected. In conclusion, poorly differentiated squamous cell carcinomas located in the palate have higher immunostaining of Bmi-1, which can characterize activation of the Epithelial-Mesenchymal Transition process in these tumors.


Assuntos
Carcinoma de Células Escamosas/patologia , Transição Epitelial-Mesenquimal , Neoplasias Bucais/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Biomarcadores Tumorais/metabolismo , Caderinas/metabolismo , Feminino , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Complexo Repressor Polycomb 1/metabolismo , Análise Serial de Tecidos
6.
Braz. dent. j ; 28(5): 543-547, Sept.-Oct. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-888684

RESUMO

Abstract The aim of this study is to evaluate the immunohistochemical expression of E-cadherin, N-cadherin and Bmi-1, and their association with clinical parameters and with the degree of histopathological differentiation in oral squamous cell carcinomas. 65 squamous cell carcinoma samples were used for constructing a tissue microarray block, and then immunohistochemistry was performed for different markers. A semi-quantitative analysis of the amount of positive tumor cells was performed by two blind and calibrated observers (Kappa>0.75). The statistical Mann-Whitney and Kruskal-Wallis tests were used to evaluate the data. The correlation between variables was investigated by the Spearman test, and the significance level set at p<0.05. We observed higher expression of Bmi-1 in tumors located in the palate (p<0.0001). In addition, poorly differentiated tumors had a greater amount of Bmi-1 positive cells (p=0.0011). Regarding the other correlations between variables, no significant associations were detected. In conclusion, poorly differentiated squamous cell carcinomas located in the palate have higher immunostaining of Bmi-1, which can characterize activation of the Epithelial-Mesenchymal Transition process in these tumors.


Resumo O objetivo deste estudo foi avaliar a associação entre a expressão imunoistoquímica de E-caderina, N-caderina e Bmi-1, com os parâmetros clínicos e o grau de diferenciação em carcinomas espinocelulares bucais. Sessenta e cinco amostras foram selecionadas para a construção de um bloco de microarranjo tecidual, e a técnica de imunoistoquímica foi realizada para os diferentes marcadores. Uma análise semi-quantitativa das células tumorais positivas foi realizada por dois observadores calibrados e cegos (Kappa>0.75). Os testes estatísticos Mann-Whitney e Kruskal-Wallis foram utilizados para a análise dos dados e a correlação entre as variáveis foi investigada com o teste de Spearman. O nível de significância foi determinado em p <0.05. Observamos maior expressão de Bmi-1 em tumores localizados em palato (p <0.0001). Além disso, tumores pobremente diferenciados apresentaram maior quantidade de células positivas para Bmi-1 (p=0.0011). Não encontramos outras correlações ou associações significativas. Em conclusão, carcinomas espinocelulares pobremente diferenciados e localizados no palato apresentam maior marcação imunoistoquímica de Bmi-1, o que pode caracterizar a ativação do processo de transição epitélio-mesênquima nesses tumores.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Carcinoma de Células Escamosas/patologia , Transição Epitelial-Mesenquimal , Neoplasias Bucais/patologia , Biomarcadores Tumorais/metabolismo , Caderinas/metabolismo , Imuno-Histoquímica , Complexo Repressor Polycomb 1/metabolismo , Análise Serial de Tecidos
7.
Artigo em Inglês | MEDLINE | ID: mdl-28411003

RESUMO

OBJECTIVES: The aim of this study was to access the prognostic value of 4 histopathologic grading systems of oral squamous cell carcinoma (OSCC): The World Health Organization (WHO), Anneroth, Bryne (1989), and Bryne (1992). STUDY DESIGN: Eighty-five cases of OSCC diagnosed between 1996 and 2010 at the Clinics Hospital of Porto Alegre (Porto Alegre, Brazil) were included. Slides stained with hematoxylin and eosin were obtained, and a histologic grade was assigned on the basis of the consensus of 3 expert oral pathologists, who were blinded to the clinicopathologic factors. Each system was correlated with proliferative labeling index, accessed through Ki67 immunostaining, clinicopathologic factors, patient outcome (alive or deceased), and survival time. RESULTS: The increase in Bryne (1992) histologic grades was accompanied by an increase in proliferative labeling index. Moreover, this system was the only one associated with patient outcome (P = .01) and survival. Bryne (1992) grading system grade III tumors were associated with poor disease-specific survival according to univariate and multivariate cox regression analyses and the log-rank test (P < .05). The other systems evaluated presented no association with patients' outcome or survival. CONCLUSIONS: The Bryne (1992) grading system is more effective in predicting survival in OSCC compared with the systems proposed by the WHO, Anneroth, or Bryne (1989).


Assuntos
Carcinoma de Células Escamosas/patologia , Neoplasias Bucais/patologia , Gradação de Tumores/métodos , Idoso , Biomarcadores Tumorais/análise , Estudos Transversais , Feminino , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Prognóstico , Estudos Retrospectivos , Análise de Sobrevida
8.
Spec Care Dentist ; 36(2): 99-103, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26597996

RESUMO

Histoplasmosis is an endemic systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum. In immunocompromised patients, histoplasmosis generally occurs as an opportunistic disease, with dissemination to various organs. Cutaneous involvement is observed in 38% to 85% of cases, with oral mucosal involvement in 30% to 60% of cases. This article describes the case study of a 32-year-old woman who presented an extensive tongue ulcer due to histoplasmosis and had the HIV infection diagnosis based on laboratory tests requested by the dentist.


Assuntos
Infecções por HIV/diagnóstico , Histoplasmose/diagnóstico , Hospedeiro Imunocomprometido , Doenças da Língua/microbiologia , Adulto , Diagnóstico Diferencial , Feminino , Humanos
10.
Porto Alegre; s.n; 2015. 43 p. ilus.
Tese em Português | BBO - Odontologia | ID: biblio-867694

RESUMO

Leucoplasia bucal (LB) é uma desordem potencialmente maligna, com risco de transformação maligna que varia de 0,13% a 17,5%. Muitos estudos vêm buscando estabelecer biomarcadores capazes de predizer o potencial de transformação maligna dessa lesão. O Ki-67 é uma proteína não-histônica nuclear que tem sido amplamente utilizada para avaliar proliferação celular. O BMI-1 é uma proteína considerada um marcador essencial para a manutenção das propriedades de autorrenovação e da tumorigenicidade do carcinoma espinocelular. O objetivo principal desse estudo observacional transversal foi avaliar proliferação e imortalização celulares em LB a partir da marcação imunoistoquímica do Ki-67 e do BMI-1, comparando lesões displásicas com não displásicas. Casos de LB não displásica - LBND (n=28), LB displásica - LBD (n=33) foram selecionados a partir de prontuários de pacientes e comparados com mucosa clinicamente normal - MN (n=9), hiperplasia inflamatória - HI (n=17) e carcinoma espinocelular - CEC (n=19). Os diagnósticos histopatológicos foram confirmados a partir da revisão de cortes histológicos corados por hematoxilina e eosina. Adicionalmente, cortes histológicos foram submetidos à técnica imunoistoquímica para avaliação de Ki-67 e BMI-1. Para a quantificação foi considerado o percentual de células positivas por 1000 células para o CEC e 1500 células para os demais grupos. O percentual de imunomarcação de Ki-67 e de BMI-1, quando avaliadas todas as camadas epiteliais em conjunto, foi mais alto no CEC quando comparado aos demais grupos (Kruskal-Wallis, p<0.05). A expressão de Ki-67 foi maior em LBND, LBD e HI quando comparada com MN (Kruskal-Wallis, p<0.05)...


Oral leukoplakia (OL) is potentially malignant disorder, with a risk of malignant transformation that ranges from 0.13% to 17.5%. Many biological markers have been used as an attempt to predict malignant transformation, but no reliable markers have been established so far. The Ki-67 is a nuclear non-histone regarded as reliable marker of proliferating cells .BMI-1 is a protein considered as an essential marker for maintenance of properties self-renewability and tumorigenicity of squamous cell carcinoma. The main aim this cross-sectional observational study was to evaluate cell proliferation and immortalization in oral leukoplakia, comparing non-dysplastic and dysplastic lesions. Cases of non-dysplastic – Non-dys OL (n=28), dysplastic – Dys OL (n=33) records were selected and compared with normal oral mucosa – NOM (n=9), inflammatory hyperplasia –IH (n=17), and oral squamous cell carcinoma - OSCC (n=19). The histopathological diagnosis was confirmed by the revision of Hematoxilin and Eosin stained slides. Additionally, histological sections were submitted to immunohistochemical technique for evaluation of Ki-67 and BMI-1. The labeling index was determined by counting the labeled nuclei of 1000 cells for OSCC cases and 1500 for the others comparison groups. Ki-67 and BMI-1 immunolabeling percentage were higher in OSCC in comparison of others groups when all epithelial layers were evaluated together (Kruskal-Wallis, p<0.05). Ki-67 immunolabeling increased in Non-dys OL, Dys OL and IH when compared to NOM (Kruskal-Wallis, p<0.05). Furthermore, BMI-1 immunolabeling was higher in Dys OL relation to NOM in the analysis of all epithelial layers together (Kruskal-Wallis, p<0.05)...


Assuntos
Carcinoma de Células Escamosas , Leucoplasia Oral , Neoplasias Bucais , Evolução Clínica
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