Salivary gland myoepithelial carcinoma

被引:22
|
作者
Vilar-Gonzalez, S. [1 ]
Bradley, K. [1 ]
Rico-Perez, J. [2 ]
Vogiatzis, P. [1 ]
Golka, D. [3 ]
Nigam, A. [3 ]
Sivaramalingam, M. [2 ]
Kazmi, S. [3 ]
机构
[1] Queen Alexandra Hosp, Portsmouth, Hants, England
[2] Royal Preston Hosp, Preston, Lancs, England
[3] Blackpool Victoria Hosp, Blackpool, Lancs, England
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2015年 / 17卷 / 11期
关键词
Salivary gland tumours; Myoepithelial carcinoma; Malignant myoepithelioma; CLEAR-CELL-CARCINOMA; MALIGNANT MYOEPITHELIOMA; PLEOMORPHIC ADENOMA; PAROTID-GLAND; LACRIMAL GLAND; TUMORS; CANCER; EXPRESSION; CHILDREN; SPECTRUM;
D O I
10.1007/s12094-015-1329-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Salivary gland myoepithelial carcinoma (MC) or malignant myoepithelioma is a rare entity. MC usually presents as a slow-growing painless mass arising in the parotid gland, but may involve other salivary glands. This tumour may be particularly locally aggressive, but its clinical and biological features are not yet fully understood. MC may arise from pre-existing benign lesions, such as pleomorphic adenomas or benign myoepitheliomas, or may arise de novo. It usually affects patients over 50 years old, with no gender preference. Because it is often asymptomatic, the presentation and diagnosis can be delayed by months, even years. The current WHO classification considers MC to be an intermediate- to high-grade malignancy. Other published data suggest it is likely to be a high-grade neoplasm, consistent with its aggressive behaviour. Its epidemiology, histopathological features, immunohistochemical profile, clinical behaviour and optimal management are not well understood. Following review of the current literature we aim to address these.
引用
收藏
页码:847 / 855
页数:9
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