Daxecker F, Felber S
Department of Ophthalmology, University of Innsbruck, Austria.
Ophthalmologica. 1993;206(3):139-42. doi: 10.1159/000310379.
Congenital anophthalmia (CA) is a rare malformation. Primary forms without development of optic nerves can be differentiated from secondary forms with rudimentary optic nerves and eye bulbi. Neuroradiologic examinations in these children are performed to differentiate primary from secondary forms and to exclude associated cerebral malformations. We report on 2 children with secondary CA, a 9-month-old girl with unilateral CA and a 3-year-old boy with bilateral CA. Magnetic resonance imaging (MRI) was superior to computerized tomography (CT) in the delineation of the rudimentary optic nerves and tracts as well as the intraorbital contents. In addition magnetic resonance images revealed partial agenesis of the corpus callosum and microgyria of the calcarine cortex in the boy. These results suggest that MRI should replace CT in the diagnosis of CA.
先天性无眼畸形(CA)是一种罕见的畸形。原发性无视神经发育的类型可与伴有发育不全的视神经和眼球的继发性类型相鉴别。对这些儿童进行神经放射学检查,以区分原发性和继发性类型,并排除相关的脑畸形。我们报告2例继发性CA患儿,1例9个月大的单侧CA女孩和1例3岁的双侧CA男孩。在显示发育不全的视神经和视束以及眶内结构方面,磁共振成像(MRI)优于计算机断层扫描(CT)。此外,磁共振图像显示该男孩胼胝体部分发育不全和距状皮质微小脑回。这些结果表明,在CA的诊断中,MRI应取代CT。