Yabuki Kei, Matsuyama Atsuji, Shiba Eisuke, Nagatani Gunji, Hisaoka Masanori
1 University of Occupational and Environmental Health, Kitakyushu, Japan.
Int J Surg Pathol. 2018 May;26(3):250-255. doi: 10.1177/1066896917742721. Epub 2017 Nov 23.
In this article, we report a case of sclerosing mucoepidermoid carcinoma (MEC) arising in the parotid gland, with CRTC1-MAML2 gene fusion. A 73-year-old woman with a mass in the right parotid region was referred to our hospital. Radiological imaging tests revealed a well-defined mass, measuring 25 mm in diameter, with foci of calcification in the deep lobe of the parotid gland, extending to the parapharyngeal space. Microscopically, the tumor was composed of a proliferation of atypical glandular epithelial cells having intracytoplasmic mucin, squamoid cells, and intermediate cells arranged in nests embedded in a fibrosclerotic stroma, associated with a dense chronic inflammatory infiltrate containing immunoglobulin G4-immunoreactive plasma cells. Reverse transcription-polymerase chain reaction analysis using a formalin-fixed, paraffin-embedded tumor tissue specimen revealed the CRTC1-MAML2 fusion gene transcript. This is the first report of sclerosing MEC with the detection of the MEC-associated fusion gene, reinforcing a common genetic association between MEC and sclerosing MEC.
在本文中,我们报告了1例发生于腮腺的伴有CRTC1-MAML2基因融合的硬化性黏液表皮样癌(MEC)。一名73岁的女性因右侧腮腺区肿物转诊至我院。影像学检查显示一个边界清晰的肿物,直径25 mm,位于腮腺深叶,伴有钙化灶,并延伸至咽旁间隙。显微镜下,肿瘤由具有胞浆内黏液的非典型腺上皮细胞、鳞状细胞和中间细胞增殖构成,这些细胞排列成巢状,包埋于纤维硬化性间质中,并伴有含有免疫球蛋白G4免疫反应性浆细胞的致密慢性炎性浸润。使用福尔马林固定、石蜡包埋的肿瘤组织标本进行逆转录-聚合酶链反应分析,发现了CRTC1-MAML2融合基因转录本。这是首例检测到MEC相关融合基因的硬化性MEC报告,进一步证实了MEC与硬化性MEC之间存在共同的基因关联。