{"title":"腮腺表皮样癌1例报告","authors":"J. Kambiré, S. Ouédraogo, M. Zida, S. Traoré","doi":"10.4172/2155-9619.1000334","DOIUrl":null,"url":null,"abstract":"Introduction: Malignant parotid tumors are rare. They are characterized by their histological diversity dominated by muco-epidermoid tumors and adenocarcinomas; squamous cell carcinomas are much rarer. Result: We report a case of carcinoma not very differentiated from the parotid evolving for 6 years to reach 15 cm of major axis at the time of its diagnosis in a 35-year-old woman. Conclusion: Epidermoid carcinomas, although rare, are not exceptional. Their management is based on total parotidectomy provided that the diagnosis is early. Population education is required for a first-line use of health services in front of any indolor swelling in the parotid region.","PeriodicalId":302578,"journal":{"name":"Journal of Nuclear Medicine and Radiation Therapy","volume":"445 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Parotid Epidermoid Carcinoma: A Case Report\",\"authors\":\"J. Kambiré, S. Ouédraogo, M. Zida, S. Traoré\",\"doi\":\"10.4172/2155-9619.1000334\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Malignant parotid tumors are rare. They are characterized by their histological diversity dominated by muco-epidermoid tumors and adenocarcinomas; squamous cell carcinomas are much rarer. Result: We report a case of carcinoma not very differentiated from the parotid evolving for 6 years to reach 15 cm of major axis at the time of its diagnosis in a 35-year-old woman. Conclusion: Epidermoid carcinomas, although rare, are not exceptional. Their management is based on total parotidectomy provided that the diagnosis is early. Population education is required for a first-line use of health services in front of any indolor swelling in the parotid region.\",\"PeriodicalId\":302578,\"journal\":{\"name\":\"Journal of Nuclear Medicine and Radiation Therapy\",\"volume\":\"445 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Nuclear Medicine and Radiation Therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2155-9619.1000334\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nuclear Medicine and Radiation Therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2155-9619.1000334","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Introduction: Malignant parotid tumors are rare. They are characterized by their histological diversity dominated by muco-epidermoid tumors and adenocarcinomas; squamous cell carcinomas are much rarer. Result: We report a case of carcinoma not very differentiated from the parotid evolving for 6 years to reach 15 cm of major axis at the time of its diagnosis in a 35-year-old woman. Conclusion: Epidermoid carcinomas, although rare, are not exceptional. Their management is based on total parotidectomy provided that the diagnosis is early. Population education is required for a first-line use of health services in front of any indolor swelling in the parotid region.
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