Kp. Cockerham et al., The clinical spectrum of schwannomas presenting with visual dysfunction: Aclinicopathologic study of three cases, SURV OPHTHA, 44(3), 1999, pp. 226-234
Schwannomas (neurilemomas) are benign tumors that arise from Schwann cells
in the peripheral nervous system. The most commonly involved nerves that ca
use neuro-ophthalmic manifestations are cranial nerves V and VIII. In this
series of three women, schwannomas presented as intraconal masses that mimi
cked a cavernous hemangioma, a superior orbital mass transgressing the supe
rior orbital fissure, and an expansive frontal lobe mass with clinical symp
toms and signs of increased intracranial pressure. Although all three compl
ained of visual blur-ring, none of our patients presented with Vth or VIIIt
h cranial nerve dysfunction. Histopathologic studies demonstrated well-circ
umscribed, encapsulated spindle-cell lesions with classic Antoni A and B pa
tterns. Histopathologic examination is essential to confirm the diagnosis o
f a schwannoma that may be otherwise clinically confusing. Direct optic ner
ve compression, globe indentation with induced hyperopia, or increased intr
acranial pressure with optic nerve compromise may be responsible for visual
symptoms. A multidisciplinary approach is often required because of the si
ze and location of schwannomas. (C) 1999 by Elsevier Science Inc. All right
s reserved.