中国口腔颌面外科杂志 ›› 2019, Vol. 17 ›› Issue (2): 190-192.doi: 10.19438/j.cjoms.2019.02.019

• 病例报告 • 上一篇    

口腔黏膜幼年性黄色肉芽肿1例报告及文献复习

戴博文, 吴汉江   

  1. 中南大学湘雅二医院 口腔颌面外科,湖南 长沙 410011
  • 收稿日期:2018-09-12 修回日期:2018-11-19 出版日期:2019-03-20 发布日期:2019-04-12
  • 通讯作者: 吴汉江,E-mail:wuhanjiang163@126.com
  • 作者简介:戴博文(1994-),男,在读硕士研究生,E-mail:793781390@qq.com.

Oral juvenile xanthogranuloma:a case report and literature review

DAI Bo-wen, WU Han-jiang   

  1. Department of Oral and Maxillofacial Surgery, The Second Xiangya Hospital of Central South University. Changsha 410011, Hunan Province, China
  • Received:2018-09-12 Revised:2018-11-19 Online:2019-03-20 Published:2019-04-12

摘要: 幼年性黄色肉芽肿是非朗格汉斯组织细胞增生症中的一种,主要发生于皮肤,可单发或多发,皮肤外器官主要累及眼、中枢神经系统、肝脏、肾脏等,口腔病变罕见。本文报告1例发生于腭部的幼年性黄色肉芽肿病例。该患儿表现为腭部黏膜下黄色结节,无明显疼痛,不影响进食及语言功能,治疗采取手术切除,术后免疫组织化学报告为幼年性黄色肉芽肿。

关键词: 幼年性黄色肉芽肿, 口腔, S100

Abstract: Juvenile xanthogranuloma (JXG) is a rare non-Langerhans cell histiocytosis that usually occurs in the skin of children, single or multiple. The systemic form of JXG affected extracutaneous sites-mostly the eyes, central nervous system, liver, kidney, etc. Oral JXG is rare. This paper reported a case with yellowish papule affecting the hard palate, without typical clinical symptoms. The lesion was surgically excised, histological and immunohistochemical analysis revealed JXG.

Key words: Juvenile xanthogranuloma, Oral cavity, S100

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