The clinical spectrum of schwannomas presenting with visual dysfunction: A clinicopathologic study of three cases

被引:24
作者
Cockerham, KP
Cockerham, GC
Stutzman, R
Hidayat, AA
Depper, MH
Turbin, RE
Kennerdell, JS
机构
[1] Allegheny Gen Hosp, Dept Ophthalmol, Pittsburgh, PA 15212 USA
[2] Ophthalmol Serv, Andrews AFB, MD USA
[3] Walter Reed Army Med Ctr, Ophthalmol Serv, Washington, DC 20307 USA
[4] Armed Forces Inst Pathol, Dept Ophthalm Pathol, Washington, DC 20306 USA
[5] Walter Reed Army Med Ctr, Dept Radiol, Washington, DC 20307 USA
关键词
neurilemoma; schwannoma; tumor;
D O I
10.1016/S0039-6257(99)00100-9
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Schwannomas (neurilemomas) are benign tumors that arise from Schwann cells in the peripheral nervous system. The most commonly involved nerves that cause neuro-ophthalmic manifestations are cranial nerves V and VIII. In this series of three women, schwannomas presented as intraconal masses that mimicked a cavernous hemangioma, a superior orbital mass transgressing the superior orbital fissure, and an expansive frontal lobe mass with clinical symptoms and signs of increased intracranial pressure. Although all three complained of visual blur-ring, none of our patients presented with Vth or VIIIth cranial nerve dysfunction. Histopathologic studies demonstrated well-circumscribed, encapsulated spindle-cell lesions with classic Antoni A and B patterns. Histopathologic examination is essential to confirm the diagnosis of a schwannoma that may be otherwise clinically confusing. Direct optic nerve compression, globe indentation with induced hyperopia, or increased intracranial pressure with optic nerve compromise may be responsible for visual symptoms. A multidisciplinary approach is often required because of the size and location of schwannomas. (C) 1999 by Elsevier Science Inc. All rights reserved.
引用
收藏
页码:226 / 234
页数:9
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