口腔医学 ›› 2026, Vol. 46 ›› Issue (4): 300-304.doi: 10.13591/j.cnki.kqyx.2026.04.011

• 病案分析 • 上一篇    下一篇

舌前区分泌性癌1例

凌风1,2,3, 张玉超1,2,3, 胡凌然1,2,3, 田颖琳1,2,3, 金佳怡1,2,3, 高允茹1,2,3, 傅瑜1,2,3()   

  1. 1 南京医科大学附属口腔医院口腔颌面外科, 江苏南京 (210029)
    2 江苏省口腔疾病研究重点实验室, 江苏南京 (210029)
    3 江苏省口腔转化医学工程研究中心, 江苏南京 (210029)
  • 收稿日期:2025-10-28 出版日期:2026-04-28 发布日期:2026-04-17
  • 通讯作者: 傅瑜 Tel:(025)69593129, E-mail:siyu_528@163.com
  • 基金资助:
    2023年度江苏省卫生健康委课题面上项目(苏卫科教2023-011号);江苏省自然科学基金及重点研发计划(BK20221300);江苏省科教能力提升工程——江苏省研究型医院(YJXYYJSDW4);江苏省医学创新中心(CXZX202227)

A case of secretory carcinoma in the anterior tongue

LING Feng1,2,3, ZHANG Yuchao1,2,3, HU Lingran1,2,3, TIAN Yinglin1,2,3, JIN Jiayi1,2,3, GAO Yunru1,2,3, FU Yu1,2,3()   

  1. Department of Oral Maxillofacial Surgery, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing 210029, China
  • Received:2025-10-28 Online:2026-04-28 Published:2026-04-17

摘要:

唾液腺分泌性癌是一种罕见的低度恶性唾液腺肿瘤,以ETV6-NTRK3融合基因为标志,2017年《WHO头颈部肿瘤分类》正式收录该类肿瘤。该肿瘤好发于腮腺,其次为下颌下腺及口腔小唾液腺,舌部原发极为罕见。文献报道的舌部病例仅有1例,且位于舌根处,舌前区原发病例尚未见报道。本文报道了1例发生于舌前区的唾液腺分泌性癌,患者为中年男性,以舌前部肿物就诊,外科手术完整切除肿瘤,术后HE染色示肿瘤呈腺管、乳头、囊状及实性等多种形态,伴嗜酸性分泌物和局部坏死,结合特征性免疫组化结果,最终确诊为唾液腺分泌性癌。病例的罕见发生部位增加了术前诊断难度,提示临床医师对舌部实性肿物需考虑分泌性癌可能。本文结合文献回顾了该类肿瘤的临床病理特征、分子机制及鉴别诊断,旨在提高对这一类肿瘤的认知,并对其在罕见部位发生保持警惕。

关键词: 唾液腺分泌性癌, 舌腺源性恶性肿瘤, ETV6, 免疫组化

Abstract:

Secretory carcinoma of the salivary gland is a rare low-grade malignant salivary gland tumor characterized by the distinctive ETV6-NTRK3 fusion gene. It was formally included in the 2017 WHO Classification of Head and Neck Tumors. This tumor most commonly arises in the parotid gland, followed by the submandibular gland and minor salivary glands of the oral cavity, with primary occurrence in the tongue being extremely rare. Only one case of tongue involvement has been reported in the literature, and that was located at the base of the tongue; no cases originating in the anterior tongue have been documented to date.This report describes a case of secretory carcinoma arising in the anterior tongue. The patient was a middle-aged male who presented with a mass in the anterior tongue. The tumor was completely resected surgically. Postoperative hematoxylin and eosin (HE) staining revealed a tumor exhibiting multiple growth patterns, including tubular, papillary, cystic, and solid architectures, accompanied by eosinophilic secretory material and focal necrosis. Combined with characteristic immunohistochemical findings, the final diagnosis was secretory carcinoma of the salivary gland. The rare site of occurrence in this case increased the difficulty of preoperative diagnosis, highlighting the need for clinicians to consider the possibility of secretory carcinoma when encountering solid masses in the tongue. This article, combined with a literature review, summarizes the clinicopathological features, molecular mechanisms, and differential diagnosis of this tumor type, with the aim of enhancing awareness of this entity and increasing vigilance regarding its occurrence at unusual sites.

Key words: secretory carcinoma of the salivary gland, malignant salivary gland tumor of the tongue, ETV6, immunohistochemistry

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