Rozenman Y, Folberg R, Nelson L B, Cohen E J
Ophthalmic Surg. 1985 Jun;16(6):372-4.
A child with a history of a monocular congenital cataract, cataract surgery and intraocular lens implantation at age three developed pseudophakic bullous keratopathy which persisted following intraocular lens removal and vitrectomy two years later. At age nine she presented to the Cornea Service at Wills Eye Hospital with painful bullous keratopathy and underwent a penetrating keratoplasty and anterior vitrectomy. The case is presented to bring attention to potential long-term corneal complications of pediatric cataract surgery with intraocular lens implantation.
一名曾患单眼先天性白内障的儿童，三岁时接受了白内障手术及人工晶状体植入，两年后出现了人工晶状体性大疱性角膜病变，在摘除人工晶状体和进行玻璃体切除术后该病变仍持续存在。九岁时，她因疼痛性大疱性角膜病变就诊于威尔斯眼科医院角膜科，并接受了穿透性角膜移植术和前部玻璃体切除术。本文报告该病例是为了引起对小儿白内障手术联合人工晶状体植入潜在长期角膜并发症的关注。
