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

被引:9
|
作者
Villeneuve, Hugo [2 ]
Tremblay, Steve [3 ,4 ]
Galiatsatos, Polymnia [5 ]
Hamel, Nancy [6 ,7 ]
Guertin, Louis [8 ]
Morency, Renald [9 ]
Tischkowitz, Marc [1 ,7 ,10 ,11 ]
机构
[1] Addenbrookes Hosp, Addenbrookes Treatment Ctr, Acad Lab Med Genet, Cambridge CB2 0QQ, England
[2] Univ Montreal, Ctr Hosp, Dept Radiat Oncol, Montreal, PQ, Canada
[3] Univ Laval, Fac Dent, Sect Stomatol Oral Pathol, Quebec City, PQ, Canada
[4] Hop Enfants Jesus, Ctr Hosp, Dept Oral & Maxillofacial Surg, Quebec City, PQ, Canada
[5] McGill Univ, Jewish Gen Hosp, Dept Med, Div Gastroenterol, Montreal, PQ H3T 1E2, Canada
[6] McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ H3T 1E2, Canada
[7] McGill Univ, McGill Program Canc Genet, Dept Human Genet & Oncol, Montreal, PQ H3T 1E2, Canada
[8] Univ Montreal, Ctr Hosp, Dept Ear Nose & Throat Surg, Montreal, PQ, Canada
[9] Ctr Hosp Univ Quebec CHUQ, Hop Hotel Dieu de Quebec, Dept Anat Pathol, Quebec City, PQ, Canada
[10] McGill Univ, Jewish Gen Hosp, Lady Davis Inst, Segal Canc Ctr, Montreal, PQ H3T 1E2, Canada
[11] Univ Cambridge, Dept Med Genet, Cambridge, England
关键词
Cowden syndrome; Retromolar trigone; Acinar carcinoma; MULTIPLE HAMARTOMA SYNDROME; SALIVARY-GLAND TUMORS; GERMLINE MUTATIONS; DISEASE; PTEN; GENE; 10Q22-23; BREAST;
D O I
10.1007/s10689-011-9472-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:691 / 694
页数:4
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