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布鲁克-施皮格勒综合征并发多发型皮肤和腮腺肿瘤:细针穿刺样本的细胞学发现及CYLD基因新突变的描述

Brooke-Spiegler syndrome presenting multiple concurrent cutaneous and parotid gland neoplasms: cytologic findings on fine-needle sample and description of a novel mutation of the CYLD gene.

作者信息

Malzone Maria Gabriella, Campanile Anna Cipolletta, Losito Nunzia Simona, Longo Francesco, Perri Francesco, Caponigro Francesco, Schiavone Concetta, Ionna Franco, Maiello Francesco, Martinuzzi Claudia, Nasti Sabina, Botti Gerardo, Fulciniti Franco

机构信息

Istituto Nazionale Tumori "Fondazione G. Pascale,", S.S.D. Di Citopatologia E S.C Di Anatomia Patologica, Napoli, Italy.

S.C Di Chirurgia Maxillo-Facciale ORL, Istituto Nazionale Tumori "Fondazione G. Pascale,", Napoli, Italy.

出版信息

Diagn Cytopathol. 2015 Aug;43(8):654-8. doi: 10.1002/dc.23275. Epub 2015 May 21.

Abstract

Multiple dermal cylindromas and membranous basal cell adenoma of parotid gland in a 67-year-old woman with Brooke-Spiegler syndrome (BSS) were examined by fine-needle cytology. Histology, immunochemistry, and CYLD germline mutation testing were also performed. Cytomorphology and immunochemistry of the two lesions showed basaloid neoplasms, remarkably similar, composed by proliferating epithelial cells of basal type accompanied by a smaller proportion of myoepithelial cells. CYLD gene showed a novel germline splice acceptor site mutation (c.2042-1G>C) with skipping of the entire exon 15. The occurrence of analogous tumors, dermal cylindromas, and membranous basal cell adenoma of the parotid gland, in the same patient may result from the action of a single gene on ontogenetically similar stem cells. Therefore, patients with BSS should be offered a genetic counselling for an early and correct diagnosis.

摘要

对一名患有布鲁克-施皮格勒综合征(BSS)的67岁女性的多个皮肤圆柱瘤和腮腺膜性基底细胞腺瘤进行了细针细胞学检查。还进行了组织学、免疫化学和CYLD种系突变检测。这两个病变的细胞形态学和免疫化学显示为基底样肿瘤,非常相似,由增殖的基底型上皮细胞组成,伴有较小比例的肌上皮细胞。CYLD基因显示出一个新的种系剪接受体位点突变(c.2042-1G>C),导致整个第15外显子缺失。同一患者出现类似肿瘤、皮肤圆柱瘤和腮腺膜性基底细胞腺瘤,可能是由于单个基因作用于个体发育上相似的干细胞所致。因此,应为BSS患者提供遗传咨询,以便早期正确诊断。

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