Simpson Roderick H W, Skálová Alena, Di Palma Silvana, Leivo Ilmo
Department of Anatomical Pathology, University of Calgary, 11th Floor, Foothills Medical Centre, 1403, 29th Street NW, Calgary, Alberta, T2N 2T9, Canada,
Virchows Arch. 2014 Oct;465(4):371-84. doi: 10.1007/s00428-014-1639-x. Epub 2014 Aug 30.
This review concentrates on the most important developments since the WHO classification of 2005. In particular, the identification of specific translocations is revolutionising the way salivary tumours are considered and will have a major impact on future diagnostic practice. This is true so far in four malignancies: mammary analogue secretory, mucoepidermoid, adenoid cystic and hyalinising clear cell carcinomas. In each, the gene rearrangement is found in 80 % or more of cases. Two 2014 publications have added further possible candidates with molecular abnormalities to the list (cribriform adenocarcinoma of the tongue and minor salivary glands and epithelial-myoepithelial carcinoma), but these findings have yet to be confirmed by other investigators. The advances in molecular pathology have also allowed re-evaluation of the morphology; for example, it is now realised that the histological spectrum of hyalinising clear cell carcinoma includes intracellular mucin in over half of cases, as well as tumours with only scanty clear cells. In a separate development, it is now proposed that salivary duct carcinoma can be subdivided along molecular lines, in ways analogous to breast cancer, suggesting new therapeutic prospects in an otherwise highly aggressive malignancy.
本综述聚焦于自2005年世界卫生组织分类以来的最重要进展。特别是,特定易位的识别正在彻底改变唾液腺肿瘤的认识方式,并将对未来的诊断实践产生重大影响。目前在四种恶性肿瘤中确实如此:乳腺样分泌癌、黏液表皮样癌、腺样囊性癌和透明细胞化生癌。在每种肿瘤中,80%或更多的病例存在基因重排。2014年的两篇出版物又在名单中增加了其他可能存在分子异常的候选肿瘤(舌和小唾液腺的筛状腺癌以及上皮-肌上皮癌),但这些发现尚未得到其他研究者的证实。分子病理学的进展也使得对形态学进行重新评估成为可能;例如,现在已经认识到,透明细胞化生癌的组织学谱包括超过半数病例中的细胞内黏液,以及仅有少量透明细胞的肿瘤。在另一项进展中, 现在有人提议,唾液腺导管癌可以按照分子特征进行细分,类似于乳腺癌的方式,这为这种原本具有高度侵袭性的恶性肿瘤带来了新的治疗前景。