Ghassemi Fariba, Bazvand Fatemeh, Hosseini Seyedeh Simindokht, Karkhaneh Reza, Ebrahimiadib Nazanin, Shekarchi Babak
Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Department of Radiology, AJA University of Medical Sciences, Tehran, Iran.
J Ophthalmic Vis Res. 2015 Apr-Jun;10(2):187-92. doi: 10.4103/2008-322X.163779.
To report three cases of optic nerve aplasia (ONA).
Herein three subjects with ONA are described, two subjects had unilateral involvement. In one of these cases, the fellow eye had an associated persistent hyperplastic primary vitreous (PHPV). The third patient had bilateral ONA with multiple intracranial anomalies. Previous reports are reviewed and reported findings are summarized. Orbital and brain magnetic resonance imaging (MRI) were normal in two of our cases and loss of corpus callosum in the third case. Narrow optic nerve was observed on the right side and normal appearance in other two patients.
The diagnosis of optic nerve abnormalities in children requires a thorough ophthalmic examination and proper ancillary testing. Although MRI is valuable in the diagnosis of associated central nervous system anomalies, the optic nerve may appear in normal size and course on MRI images and thus one may not be able to diagnose ONA in eyes with opaque media.
报告三例视神经发育不全(ONA)病例。
本文描述了三例患有ONA的患者,其中两例为单侧受累。在其中一例中,对侧眼伴有永存原始玻璃体增生症(PHPV)。第三例患者为双侧ONA并伴有多种颅内异常。回顾了既往报告并总结了报告结果。我们的两例患者眼眶和脑部磁共振成像(MRI)正常,第三例患者胼胝体缺失。右侧观察到视神经变窄,另外两名患者外观正常。
儿童视神经异常的诊断需要进行全面的眼科检查和适当的辅助检查。虽然MRI在诊断相关中枢神经系统异常方面很有价值,但视神经在MRI图像上可能显示大小和走行正常,因此对于介质混浊的眼睛可能无法诊断ONA。