颅面部骨纤维异常增殖症合并急性可逆性视力丧失：两例报告
Craniofacial fibrous dysplasia complicated by acute, reversible visual loss: report of two cases.
作者信息
Papadopoulos M C, Casey A T, Powell M
机构信息
Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, UK.
出版信息
Br J Neurosurg. 1998 Apr;12(2):159-61. doi: 10.1080/02688699845320.
PMID:11013671
Abstract
We report two cases of craniofacial fibrous dysplasia which presented with acute visual loss. The first patient had a sphenoid sinus mucocele compressing the optic chiasm. In the second patient the optic canal was narrowed by dysplastic bone. In both cases optic nerve decompression restored vision to normal.
摘要
我们报告了两例出现急性视力丧失的颅面骨纤维发育不良病例。第一例患者有蝶窦黏液囊肿压迫视交叉。第二例患者的视神经管因发育异常的骨骼而变窄。在这两例中，视神经减压均使视力恢复正常。
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