中医眼耳鼻喉杂志2026，Vol.16Issue(1)：63-66,4.DOI:10.3969/j.issn.1674-9006.2026.01.018
睑板神经纤维瘤及全身神经纤维瘤病1例并文献复习
A case of tarsus neurofibroma and generalized neurofibromatosis with literature review
陈安琪 1郭传恒 2莫亚 1李罗翔3
作者信息
- 1. 610072,四川成都,成都中医药大学附属医院眼科||610075,四川成都,成都中医药大学眼科学院
- 2. 610072,四川成都,成都中医药大学附属医院眼科||266000,山东青岛,青岛市黄岛区中医医院
- 3. 610072,四川成都,成都中医药大学附属医院病理科
- 折叠
摘要
Abstract
Neurofibromatosis type Ⅰ(NF1)is a multisystemic genetic disorder caused by mutations in the neurofi-bromatosis protein 1 gene located on chromosome 17.Neurofibromas occurring in the eye are relatively rare,and those in the lid area in particular are difficult to distinguish from other common swellings such as eyelid chalazion.As a result,cli-nicians often lack sufficient experience to properly intervene in patients.In this report,we report the case of a 31-year-old male patient who presented to our hospital with a limited painless swelling in the lateral canthus of the upper lid of his left eye that had persisted for 1 year.He had systemic signs of NF1,including cutaneous neurofibromas and iris Lisch nod-ules,which were biopsied after surgery.During the follow-up period,the patient's postoperative recovery was favorable,and there were no signs recurrence in the eyelid skin at six-month follow-up.In addition to reporting this case,we per-formed a comprehensive literature review of previously reported cases of ocular neurofibromas.关键词
睑板神经纤维瘤/Lisch结节/Ⅰ型神经纤维瘤病Key words
Tarsus neurofibroma/Lisch's node/Type Ⅰ neurofibromatosis分类
医药卫生引用本文复制引用
陈安琪,郭传恒,莫亚,李罗翔..睑板神经纤维瘤及全身神经纤维瘤病1例并文献复习[J].中医眼耳鼻喉杂志,2026,16(1):63-66,4.
