Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?

Springer Science and Business Media LLC - Tập 10 - Trang 691-694 - 2011
Hugo Villeneuve1, Steve Tremblay2,3, Polymnia Galiatsatos4, Nancy Hamel5,6, Louis Guertin7, Renald Morency8, Marc Tischkowitz6,9,10,11
1Department of Radiation Oncology, Centre Hospitalier de L’Université de Montréal, Montreal, Canada
2Section of Stomatology (Oral Pathology), Faculty of Dentistry, Université Laval, Quebec, Canada
3Department of Oral and Maxillofacial Surgery, Centre hospitalier affilié, Hôpital de l’Enfant-Jésus, Quebec, Canada
4Division of Gastroenterology, Department of Medicine, Jewish General Hospital, Montreal, Canada
5The Research Institute, McGill University Health Centre, Montreal, Canada
6Department of Human Genetics and Oncology, McGill Program in Cancer Genetics, McGill University, Montreal, Canada
7Department of Ear, Nose and Throat Surgery, Centre hospitalier de l’Université de Montreal, Montreal, Canada
8Département d’anatomo-pathologie, Hôpital Hotel-Dieu-de-Québec, Centre Hospitalier Universitaire du Québec (CHUQ), Quebec, Canada
9Segal Cancer Centre, Lady Davis Institute, Jewish General Hospital, Montreal, Canada
10Department of Medical Genetics, University of Cambridge, Cambridge, UK
11Academic Laboratory of Medical Genetics, Level 6, Addenbrooke’s Treatment Centre, Addenbrooke’s Hospital, Cambridge, UK

Tóm tắt

Cowden syndrome (CS) is a cancer predisposition syndrome caused by germline mutations in the PTEN tumor suppressor gene. It is associated with an increased risk of thyroid, breast and endometrial cancer but many manifestations can be found in the head and neck region, some of which are pathognomonic. Here we report a 35-year-old male referred by his dentist for evaluation of a lesion located near the retromolar trigone. Comprehensive clinical examination revealed papillomatous skin lesions, macrocephaly and gingival hypertrophy. Histopathological examination of the lesion showed an acinic cell carcinoma (ACC) of minor salivary gland origin. Analysis of the PTEN gene identified a germline R130Q mutation in exon 5, confirming the diagnosis of CS, but no loss of heterozygosity was seen in DNA extracted from tumor tissue. This is to our knowledge the first case describing an association of ACC of the minor salivary gland with a PTEN-gene related disorder. It emphasizes the importance of head and neck examination in these patients.

Tài liệu tham khảo

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