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眼眶囊性施万瘤

Cystic schwannoma of the orbit.

作者信息

Lam D S, NG J S, To K F, Abdulah V, Liew C T, Tso M O

机构信息

Department of Ophthalmology and Visual Sciences, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, N.T., Hong Kong.

出版信息

Eye (Lond). 1997;11 ( Pt 6):798-800. doi: 10.1038/eye.1997.208.

Abstract

Cystic schwannoma of the orbit is unreported in the world literature. A 54-year-old Caucasian man presented to our clinic with a 5 year history of progressive right-sided proptosis and diplopia. A large paramedian cystic mass displacing the right globe downwards and laterally was demonstrated. From the clinical and radiological features, the presumptive diagnosis of right frontal sinus mucocoele was made. However, the excisional biopsy of the lesion revealed the rare diagnosis of cystic schwannoma, arising from a branch of the first division of the trigeminal nerve. Post-operatively, the patient had a smooth recovery with visual acuity of 20/20 in each eye; full binocular single vision was also re-established. The differential diagnoses of cystic orbital mass, and the radiological and histological findings of the lesion, are described and discussed.

摘要

眼眶囊性神经鞘瘤在世界文献中尚无报道。一名54岁的白种男性因右侧进行性眼球突出和复视5年就诊于我们的诊所。检查发现一个位于中线旁的巨大囊性肿块,将右侧眼球向下和向外推移。根据临床和放射学特征,初步诊断为右额窦黏液囊肿。然而,病变的切除活检显示为罕见的囊性神经鞘瘤,起源于三叉神经第一分支。术后,患者恢复顺利,双眼视力均为20/20;双眼单视功能也得以重建。本文描述并讨论了眼眶囊性肿块的鉴别诊断以及该病变的放射学和组织学表现。

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