论文部分内容阅读
隐眼球症是一种罕见的眼球发育异常,可能是一种眼部孤立的畸形或合并其他部位的畸形,形成隐眼球综合症。1872年Eehender首先提出了隐眼球症的诊断。本文报告一例单侧隐眼球病例如下; 患者男性,6岁,汉族,新疆籍,出生后左侧无眼球,下睑皮下可见一圆形隆起物,随眼龄而渐增大。检查:左眼睑,睑裂、睫毛均正常,小角膜,透明,前房正常,虹膜4～5点处缺损,瞳孔呈梨形,光反射存在,眼底呈豹纹状。左眼睑长2cm(对侧为2.7cm),睫毛排列较对侧稀疏,下眼睑向前隆起,可触及一囊样物,随对侧眼球运动略有活动,暴露于光亮
Hidden eye disease is a rare eye developmental abnormalities, may be an eye isolated deformity or other parts of the deformity, the formation of hidden eye syndrome. 1872 Eehender first proposed the diagnosis of occult eye disease. This article reports a case of unilateral occultophthalmia as follows; Male patients, 6 years old, Han nationality, Xinjiang nationality, no left eye after birth, under the eyelid can be seen a subcutaneous sublift, with age and gradually increased. Check: left eyelid, palpebral fissure, eyelashes are normal, small cornea, transparent, anterior chamber normal, iris defect 4 to 5 points, the pupil was pear-shaped, light reflection exists, the fundus was leopard-like. Left eyelid length 2cm (contralateral 2.7cm), eyelashes sparse than the other side of the arrangement, the lower eyelid forward bulge, can reach a bag of samples, with the contralateral eye movement slightly activity, exposure to light