Research Article
Clinico-Pathological Differences of Oral Squamous Cell Carcinoma among Younger and Older Patients
1Dental Implant Research Center, Department of Oral and Maxillofacial Pathology, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran
2Dental Materials Research Center, Department of Oral and Maxillofacial Pathology, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran
- *Corresponding Author:
- Saeedeh Khalesi
Dental Materials Research Center, Department of Oral and Maxillofacial Pathology
School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran
Tel: 989131079487
E-mail: S_khalesi@dnt.mui.ac.ir
Received date: June 02, 2017; Accepted date: July 14, 2017; Published date: July 17, 2017
Citation: Razavi SM, Khalesi S (2017) Clinico-Pathological Differences of Oral Squamous Cell Carcinoma among Younger and Older Patients. J Clin Exp Pathol 7:316. doi: 10.4172/2161-0681.1000316
Copyright: © 2017 Razavi SM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Introduction: Over 95% of the oral cancers are squamous cell carcinoma (OSCC). The incidence of OSCC in earlier than 40 years old has been reported from 0.4 to 3.9% of all patients. Recent studies have indicated the increasing number of young and very elderly adults. The purpose of this study is evaluating the clinicopathological features of OSCC among younger and older patients.
Materials and Methods: In this retrospective study, files of 80 OSCC patients were retrieved from Oral Pathology Department. Demographic data including gender, age, clinical feature and location of lesions were collected. Archival formalin fixed paraffin embedded tissue blocks were used to prepare hematoxylin and eosin stained for grading OSCC based on Broder’s, Anneroth et al. and Bryne et al. classification among younger and older patients. The variables data were analyzed using Chi square, Mann Whitney and Fisher exact tests. The significant level was set at P<0.05.
Results: Comparison of clinical criteria between young and old patients did not appear statistically significant). Furthermore, we did not found a statistically significant between Broder’s, Anneroth et al. and Bryne et al. grading systems on two groups (P>0.05).
Conclusion: Within the limitations of the present study, we show that there are not any specific histpathological parameters of OSCC in young and old patients. The incidence of OSCC in young patients was low compared to old patients. Although, further research need to access genetic, hereditary, diet and demographic factors with more patients.