左舌下腺原发性成釉细胞瘤1例报告

doi:10.19438/j.cjoms.2018.05.020

中国口腔颌面外科杂志 ›› 2018, Vol. 16 ›› Issue (5): 478-480.doi: 10.19438/j.cjoms.2018.05.020

• 病例报告 • 上一篇

左舌下腺原发性成釉细胞瘤1例报告

马超¹, 焦建军¹, 靳书滨¹, 王静², 程兵坤¹

1.邯郸市中心医院口腔颌面外科,2.病理科,河北邯郸 056000

收稿日期:2018-04-10 出版日期:2018-09-20 发布日期:2018-11-06
通讯作者: 焦建军,E-mail：910317769@qq.com
作者简介:马超（1981-）,男,本科,主治医师,E-mail：40505357@qq.com

Peripheral ameloblastoma in the sublingual gland: report of one case

MA Chao¹, JIAO Jian-jun¹, JIN Shu-bin¹, WANG Jing², CHENG Bing-kun¹

1.Department of Oral and Maxillofacial Surgery, 2.Department of Pathology, Handan Central Hospital. Handan 056000, Hebei Province, China

Received:2018-04-10 Online:2018-09-20 Published:2018-11-06

摘要/Abstract

摘要： 本文报告1例原发于舌下腺的成釉细胞瘤患者。查体见该患者左侧口底相当于左舌下腺区一卵圆形肿物,影像学检查显示肿物位于左舌下腺区,未侵及下颌骨,上、下颌颌骨无明显异常。完善术前检查,明确无绝对禁忌证后手术治疗。组织学检查显示肿物与舌下腺密切相关,且符合成釉细胞瘤病理表现。术后7 d患者伤口愈合良好出院,术后随访5个月肿瘤无复发。

关键词: 舌下腺, 外周型成釉细胞瘤, 龈外外周型成釉细胞瘤

Abstract: This paper described a patient who suffered from ameloblastoma in the sublingual gland. Clinical examination found an oval-shaped mass in the left floor of the mouth. Imaging examination revealed that the mass located in the left sublingual gland area and did not invade the mandible. Preoperative examinations confirmed that there were no surgical contraindications, then surgical removal of the tumor was performed, and there was no evidence of recurrence 5 months after surgery. Histological examination showed that the tumor was closely related to the sublingual gland, the final pathologic diagnosis was peripheral ameloblastoma.

Key words: Sublingual gland, Peripheral ameloblastoma, Extragingival peripheral ameloblastoma

中图分类号:

R739.8

马超, 焦建军, 靳书滨, 王静, 程兵坤. 左舌下腺原发性成釉细胞瘤1例报告[J]. 中国口腔颌面外科杂志, 2018, 16(5): 478-480.

MA Chao, JIAO Jian-jun, JIN Shu-bin, WANG Jing, CHENG Bing-kun. Peripheral ameloblastoma in the sublingual gland: report of one case[J]. China J Oral Maxillofac Surg, 2018, 16(5): 478-480.

参考文献

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左舌下腺原发性成釉细胞瘤1例报告

Peripheral ameloblastoma in the sublingual gland: report of one case

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