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起源于上斜肌的眼眶神经鞘瘤。

Orbital schwannoma originating from the superior oblique muscle.

作者信息

Li Jia, Lin Jing, Liu Rongjiao, Li Jianqun, Yan Jianhua

机构信息

From the *State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou; and †Department of Ophthalmology, Guangzhou First People's Hospital, Guangzhou, the People's Republic of China.

出版信息

J Craniofac Surg. 2015 Mar;26(2):559-60. doi: 10.1097/SCS.0000000000001230.

Abstract

PURPOSE

Orbital schwannoma in extraocular muscles is quite rare. In this study, we describe what, to the best of our knowledge, represents the first report of a schwannoma in the superior oblique muscle.

METHODS

A case report relating clinical features as well as radiologic, surgical, and histologic findings is presented.

RESULTS

A 27-year-old man presented with a 2-year history of progressive swelling in the left upper eyelid. A smooth mass was palpable within the superior nasal orbit. The left eye was slightly displaced inferiorly, and upward gaze was mildly impaired. There was no strabismus in the primary position. Magnetic resonance imaging revealed a well-defined mass in the left superior orbit measuring 32 × 18 × 8 mm, with a high T2 signal and low-to-moderate signal on T1. A left anterior orbitotomy was performed, and the tumor was completely resected. The mass originated from the tendon of the superior oblique muscle, and histologic diagnosis confirmed a schwannoma of Antoni type A. After this procedure, all symptoms were relieved and left superior oblique function was normal. No recurrence was evident at 6 months after surgery.

CONCLUSIONS

This rare case demonstrates that orbital schwannoma may occur in association with the superior oblique muscle. With careful surgical dissection, normal function of the involved muscle can be restored.

摘要

目的

眼外肌眶内神经鞘瘤十分罕见。在本研究中,据我们所知,我们描述了首例发生于上斜肌的神经鞘瘤。

方法

呈现一例报告,涉及临床特征以及放射学、手术和组织学检查结果。

结果

一名27岁男性,左上眼睑渐进性肿胀2年。在鼻上眶可触及一光滑肿物。左眼轻度向下移位,向上注视轻度受限。原在位无斜视。磁共振成像显示左眶上部有一界限清晰的肿物,大小为32×18×8mm,T2加权像呈高信号,T1加权像呈低至中等信号。行左前眶切开术,肿瘤被完全切除。肿物起源于上斜肌腱,组织学诊断为Antoni A型神经鞘瘤。术后所有症状缓解,左上斜肌功能正常。术后6个月未见复发。

结论

这一罕见病例表明眶内神经鞘瘤可与上斜肌相关联。通过仔细的手术分离,受累肌肉的正常功能可得以恢复。

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