Mucoepidermoid carcinoma: A yet unreported cancer associated with familial adenomatous polyposis

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TitreMucoepidermoid carcinoma: A yet unreported cancer associated with familial adenomatous polyposis
Type de publicationJournal Article
Year of Publication2014
AuteursCazorla A, Viennet G, Uro-Coste E, Valmary-Degano S
JournalJOURNAL OF CRANIO-MAXILLOFACIAL SURGERY
Volume42
Pagination262-264
Date PublishedAPR
Type of ArticleArticle
ISSN1010-5182
Mots-clésGardner's syndrome, Mucoepidermoid carcinoma, Turcot's syndrome
Résumé

Turcot's syndrome is a rare clinical syndrome, characterized by the association between familial adenomatous polyposis (FAP) and a primary central nervous system tumour. Gardner's syndrome is characterized by the association between FAP and several tumour types such as multiple osteomas, fibromas, epidermoid cysts and desmoid tumours. We report here the case of a twenty-six year-old woman with a history of both Turcot's and Gardner syndromes. She had a family history of adenomatous polyposis with a mutation in the APC (Adenomatous Polyposis Coli) gene. At the age of 26, she presented a mucoepidermoid carcinoma of the right parotid gland in which the MECT1-MAML2 fusion was showed. We discuss the possible addition of this latter cancer type in the definition of Gardner's syndrome. (C) 2013 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.

DOI10.1016/j.jcms.2013.05.012