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Niger J Clin Pract ; 25(9): 1424-1429, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36149200

RESUMO

Background: Identifying tumor markers that can be used to determine the biological behavior of tumors and predicting their prognosis may be helpful in choosing treatment strategies. Besides the differences in the embryological and histological anatomy of the larynx in this regard, the possibility of molecular causes that can explain the different clinical behaviors has always been a question for the scientific world. Aim: In this study, we aimed to investigate whether there were any immunohistochemically molecular differences among laryngeal carcinoma cases originating from two different anatomical regions of the larynx. Patients and Methods: The study group consisted of 43 patients. The rate of supraglottic cancers was 41.8%, while the rest had glotto-subglottic tumors. Ki67, ß-catenin, E-cadherin, and p53 were examined in pathology preparations obtained by laryngectomy surgeries. The data obtained were analyzed by comparing factors that may affect the prognosis of the disease and between tumors originating from the two different anatomical regions. Results: We did not see any statistically significant difference between groups for stage and grade of tumor, tumor recurrence rate, or lymphovascular or perineural invasion rated in terms of the investigated markers. In addition, there was no statistically significant difference between the two distinct groups in survival analysis. Conclusions: With these results, our study differs from some studies in the literature, and we think that this difference could be because the cases in our study consisted of advanced stage tumors and the groups investigated had similar survival rates.


Assuntos
Carcinoma , Neoplasias Laríngeas , Laringe , Biomarcadores Tumorais , Caderinas/metabolismo , Carcinoma/patologia , Humanos , Antígeno Ki-67/metabolismo , Neoplasias Laríngeas/patologia , Neoplasias Laríngeas/cirurgia , Laringe/metabolismo , Laringe/patologia , Recidiva Local de Neoplasia/patologia , Prognóstico , Proteína Supressora de Tumor p53 , beta Catenina/metabolismo
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