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1.
J Evid Based Dent Pract ; 23(4): 101898, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-38035889

RESUMO

BACKGROUND: Evidence suggests that inflammation contributes to tumor development, from onset to progression and metastasis. Platelet-to-lymphocyte ratio (PLR) is a composite parameter that provides information from two distinct cellular elements, platelets, and lymphocytes. The purpose of this systematic review and meta-analysis is to evaluate the prognostic role of the PLR, in terms of overall survival (OS), disease-free survival (DFS), cancer-specific survival (CSS) and progression-free survival (PFS), in patients with primary head and neck squamous cell carcinoma treated with surgery followed or not by adjuvant therapies. MATERIALS AND METHODS: This systematic review was performed according to the guidelines reported in the Cochrane Handbook and the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement. Meta-analysis of OS and DFS was performed using the inverse of variance test. Random-effect models were used on the basis of high heterogeneity. Risk of bias assessment, quality of evidence within studies (GRADE) and trial sequential analysis (TSA) were also performed. RESULTS: The analysis revealed that a higher value of pretreatment PLR correlates with a statistically significant decrease of OS (HR, 1.85; 95% CI: [1.23, 2.80]; P < .00001), confirmed by TSA. The meta-analysis reports an association between high PLR and DFS (HR,1.46; 95% CI: [1.03, 2.06]; P = .003); but TSA suggests that it his should be considered as a false positive. Further studies are needed to validate the efficacy of PLR in predicting CSS and PFS outcomes. CONCLUSION: Pretreatment PLR is an independent prognostic factor for OS in HNSCC.


Assuntos
Neoplasias de Cabeça e Pescoço , Linfócitos , Humanos , Carcinoma de Células Escamosas de Cabeça e Pescoço/patologia , Prognóstico , Linfócitos/patologia , Plaquetas/patologia , Neoplasias de Cabeça e Pescoço/patologia , Neutrófilos/patologia
2.
J Craniofac Surg ; 33(4): e431-e433, 2022 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-34759253

RESUMO

ABSTRACT: Intravascular papillary endothelial hyperplasia (IPEH) is a lesion characterized by the proliferation of endothelial cells within the lumen of the vessel, it was first described by Masson in 1923.The pathogenesis of Masson's tumor is still unknown, currently the most accredited hypothesis is the reactive 1. Clinically and symptomatologically it can have different presentations, it is, therefore, of fundamental importance to make a correct differential diagnosis. Diagnosis is mainly based on histological criteria. Intravascular papillary endothelial hyperplasia usually occurs in the skin and subcutaneous tissues, less commonly in the skeleton. The present is the fifth case of intravascular papillary endothelial hyperplasia of the mandible.


Assuntos
Hemangioendotelioma , Neoplasias Vasculares , Diagnóstico Diferencial , Células Endoteliais , Hemangioendotelioma/diagnóstico , Hemangioendotelioma/patologia , Hemangioendotelioma/cirurgia , Humanos , Hiperplasia/patologia , Mandíbula/patologia , Neoplasias Vasculares/patologia
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