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原发性视神经鞘脊索样脑膜瘤。

A primary optic nerve sheath chordoid meningioma.

机构信息

Neurosurgery Services, Department of Surgical Oncology, Room 48, Main Building, Tata Memorial Hospital, E Borges Road, Parel, Mumbai 400 012, India.

出版信息

J Clin Neurosci. 2010 Mar;17(3):397-9. doi: 10.1016/j.jocn.2009.05.035. Epub 2010 Jan 13.

Abstract

Primary optic nerve sheath meningiomas (ONM) are rare. Most of these are World Health Organization Grade I meningiomas. Because of the intimate relationship to the optic nerve sheath from which they arise, radical excision is often not feasible. The chordoid variant of meningioma is an infrequent tumor and extremely uncommon among primary ONMs. We report a 36-year-old woman with painless proptosis and normal visual acuity who presented to us with an exophytic intraconal mass, which was excised. Histology revealed a chordoid meningioma. We could find only two previous reports, which are discussed.

摘要

原发性视神经鞘脑膜瘤(ONM)较为罕见。其中大多数为世界卫生组织分级 I 级脑膜瘤。由于与起源的视神经鞘关系密切,根治性切除往往不可行。脊索样脑膜瘤是一种罕见的肿瘤,在原发性 ONM 中极为罕见。我们报告了一例 36 岁女性,表现为无痛性眼球突出和正常视力,就诊时发现眶内突出的肿块,予以切除。组织学显示为脊索样脑膜瘤。我们仅发现两例既往报道,一并进行了讨论。

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