可能由多形性腺瘤引起的唾液管癌1例

Dedy Ariwansa, Durga Paudel, Tetsuro Morikawa, Koki Yoshida, Ariuntsetseg Khurelchuluun, Shuhei Takahashi, J. Sato, E. Nakayama, H. Nagayasu, Yoshihiro Akbiko
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摘要

目的:我们报告一例罕见的涎腺管癌,可能是由癌外多形性腺瘤的恶性成分引起的。方法:一名56岁的日本男性,自诉左侧下颚肿胀2年,直到2日前无痛。口外检查,面部两侧不对称。超声示左侧腮腺1.5x2.5x2.5 cm低回声肿块。CT显示左侧腮腺有轻微不规则肿块,未见邻近组织浸润。在此基础上,诊断为左腮腺良性肿瘤。结果:全麻下行手术切除。组织病理学检查,结缔组织纤维成分丰富,伴透明。观察到高异型性上皮细胞以索状浸润性增生进入结缔组织。导管内部分为罗马桥式结构,中心部分呈渐进式坏死。基于这些发现,我们最终诊断为可能由多形性腺瘤引起的唾液管癌。P16高甲基化是口腔恶性肿瘤的一种已知现象。我们还检查了p16基因的甲基化状态,发现在该肿瘤中存在高水平的甲基化。结论:我们报告了一例可能由多形性腺瘤引起的罕见的涎腺癌,并证实了肿瘤中p16基因的高甲基化水平。
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A case of salivary duct carcinoma possibly arising from pleomorphic adenoma
Objective: We report a rare case of salivary duct carcinoma possibly arising from the malignant component of carcinoma ex pleomorphic adenoma. Methods: A 56-year-old Japanese male complained of swelling in the left side of jaw for 2 years which was painless until 2 days ago. On extraoral examination, the face was bilaterally asymmetrical. An ultrasonography revealed hypoechoic mass of size 1.5x2.5x2.5 cm on left parotid gland. Computed tomography (CT) revealed a slight irregular mass on left parotid gland with no infiltration to adjacent tissues. Based on these findings, a clinical diagnosis of left parotid benign tumor was made. Results: A surgical excision was performed under general anesthesia. On histopathological examination, the connective tissue was rich in fibrous components and was accompanied by hyaline. Epithelial cells with high atypia proliferating invasively as cords into connective tissue were observed. The intraductal component had Roman-bridge-like architecture with central portion undergoing comedonecrosis. Based on these findings, a final diagnosis of salivary duct carcinoma possibly arising from pleomorphic adenoma was made. p16 hypermethylation is a known phenomenon in oral malignancy. We also checked the methylation status of p16 gene and found high level of methylation in this tumor. Conclusion: We reported a rare case of salivary duct carcinoma possibly arising from pleomorphic adenoma and also demonstrated high methylation level of p16 gene in the tumor.
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