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舌下腺黏液表皮样癌伴 基因易位:一例报告。 (原文中“the gene”处信息缺失)

Mucoepidermoid carcinoma of the sublingual gland harboring a translocation of the gene: A case report.

作者信息

Sato Kiminobu, Akiba Jun, Nakamura Ken, Abe Hideyuki, Kawahara Akihiko, Aso Takeichiro, Umeno Hirohito, Harada Hiroshi, Yano Hirohisa

机构信息

Department of Otolaryngology-Head and Neck Surgery, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.

Department of Pathology, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.

出版信息

Oncol Lett. 2017 Sep;14(3):2970-2974. doi: 10.3892/ol.2017.6550. Epub 2017 Jul 8.

Abstract

Among tumors of the major salivary glands, tumors in the sublingual gland are rare. Although mucoepidermoid carcinoma (MEC) represents a histological type of salivary gland tumor, it is occasionally difficult to diagnose due to its histological variation. The present study reports a case of MEC harboring a mastermind-like transcriptional coactivator 2 () gene translocation in the sublingual gland. A 76-year-old Japanese woman with a mass in the left submandibular region was referred to Kurume University Hospital (Kurume, Japan). Computed tomography scans revealed that the tumor was predominantly located in the sublingual gland, and tumor resection was performed. Histologically, the tumor was composed of cells that exhibited low-grade nuclear atypia and clear and/or granular eosinophilic cytoplasm, and that were proliferating in solid patterns. Periodic acid-Schiff and alcian blue staining revealed a small number of mucinous cells in the tumor. Immunohistochemically, the tumor cells were positive for p40 and p63. Fluorescence hybridization (FISH) analysis revealed a gene split. The definitive pathological diagnosis was low-grade MEC, as the case lacked any factors indicative of high-grade malignancy. To the best of our knowledge, this is the first report of MEC in the sublingual gland with gene translocation confirmed by FISH.

摘要

在大唾液腺肿瘤中,舌下腺肿瘤较为罕见。尽管黏液表皮样癌(MEC)是唾液腺肿瘤的一种组织学类型,但由于其组织学变异,有时诊断困难。本研究报告了一例发生于舌下腺的伴有主脑样转录共激活因子2()基因易位的黏液表皮样癌病例。一名76岁的日本女性因左下颌下区肿物被转诊至久留米大学医院(日本久留米)。计算机断层扫描显示肿瘤主要位于舌下腺,遂行肿瘤切除术。组织学上,肿瘤由核异型性低、胞质清亮和/或嗜酸性颗粒状、呈实性增殖的细胞组成。过碘酸-希夫染色和阿尔辛蓝染色显示肿瘤中有少量黏液细胞。免疫组化显示肿瘤细胞p40和p63呈阳性。荧光原位杂交(FISH)分析显示有基因断裂。最终病理诊断为低级别黏液表皮样癌,因为该病例缺乏任何提示高级别恶性的因素。据我们所知,这是首例经FISH证实伴有基因易位的舌下腺黏液表皮样癌报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/372c/5588114/b185ca2cfbc1/ol-14-03-2970-g00.jpg

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