Kazim M, Kennerdell J S, Maroon J, Rothfus W, Marquardt M
Department of Ophthalmology, Columbia University, New York, NY.
Arch Ophthalmol. 1992 Feb;110(2):236-8. doi: 10.1001/archopht.1992.01080140092034.
A 21-year-old patient with a biopsy-proved choristomatous malformation of the optic nerve and chiasm is presented. The patient experienced progressive unilateral vision loss and optic atrophy. A gadolinium-enhanced magnetic resonance image demonstrated chiasmal involvement that was not evident on computed tomographic scan or visual field testing. We believe this is the third reported case of a choristomatous malformation of the optic nerve and chiasm and the first report of magnetic resonance imaging findings.
本文报告了一名21岁经活检证实患有视神经和视交叉迷芽瘤畸形的患者。该患者经历了渐进性单侧视力丧失和视神经萎缩。钆增强磁共振成像显示视交叉受累,这在计算机断层扫描或视野检查中并不明显。我们认为这是第三例报告的视神经和视交叉迷芽瘤畸形病例,也是磁共振成像结果的首次报告。