伴发腮腺低级别黏液表皮样癌和导管内癌:病例报告并简要回顾

Harada H, G. S., Kudo N, N. S, H. K, M. A, Kurose A
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引用次数: 0

摘要

患者为日本女性,曾为癌症甲状腺患者。计算机断层扫描显示,癌症治疗后约14年,右腮腺有一个小肿块。增强磁共振成像怀疑为多形性腺瘤。三年后,当她60岁时,细针抽吸细胞学检查未能确定诊断,于是进行了腮腺浅表切除术。此后约2年没有复发或转移的迹象。组织学检查显示腮腺肿块内同时存在两种组织学类型的低度黏液表皮样癌和低度导管内癌。尽管位置较近,但这两种类型的癌没有混合。粘液表皮样癌形成多房囊性结构,其中粘液性、中间性和非角化鳞状细胞混杂。导管内癌中唯一占主导地位的导管内生长表现为筛状和乳头状囊性模式的结合以及S100蛋白的弥漫性阳性反应。荧光原位杂交显示粘液表皮样癌具有MAML2基因的分裂信号,但在导管内癌中未检测到MAML2和ETV6基因的分裂信息。我们讨论了本病例的组织形态学特征和诊断问题,并简要回顾了文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concomitant Low-Grade Mucoepidermoid and Intraductal Carcinomas the Parotid Gland: Case Presentation with a Brief Review
The patient was a Japanese female and a former thyroid cancer patient. A computed tomography scan indicated a small mass in the right parotid gland about 14 years after therapy for thyroid cancer. Pleomorphic adenoma was suspected by contrast-enhanced magnetic resonance imaging. Three years later, when she was 60 years old, fine needle aspiration cytology failed to determine a diagnosis and superficial parotidectomy was performed. There have been no signs of recurrence or metastasis for about 2 years thereafter. Histological examination revealed two histological types of low-grade mucoepidermoid carcinoma and low-grade intraductal carcinoma coexisting within the parotid mass. Although closely located, the two types of carcinoma had not intermingled. The mucoepidermoid carcinoma formed multilocular cystic structures, in which mucous, intermediate, and non-keratinizing squamous cells were intermingled. Exclusively predominant intraductal growth in the intraductal carcinoma showed a combination of cribriform and papillary-cystic patterns and diffuse positive reaction for S100 protein. Fluorescence in situ hybridization demonstrated the mucoepidermoid carcinoma had split signals for the MAML2 gene but no split signals were detected for the MAML2 and ETV6 genes in the intraductal carcinoma. We discuss the histomorphological features and diagnostic problems of the present case and the literature is briefly reviewed.
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