Abdel-Hafez Ghada, Wilson M Edward, Trivedi Rupal H
Miles Center for Pediatric Ophthalmology, Storm Eye Institute, Department of Ophthalmology, Medical University of South Carolina, Charleston, South Carolina.
J AAPOS. 2010 Feb;14(1):81-2. doi: 10.1016/j.jaapos.2009.10.009.
An 8-month-old boy was found to have unilateral persistent fetal vasculature (PFV) and a small visually insignificant lens opacity. No changes were noted in the appearance of the eye on examinations up to age 3 years. At the age of 4 years, a posterior lentiglobus requiring surgical intervention developed. The thinned and bulging posterior capsule ruptured at surgery. PFV, when treated conservatively, has not been reported to lead to progressive lentiglobus. This case documents the rare concurrence of PFV and lentiglobus.
一名8个月大的男孩被发现患有单侧永存原始玻璃体增生症（PFV）以及一个在视觉上无明显影响的小晶状体混浊。在3岁前的检查中，眼睛外观未发现变化。4岁时，出现了需要手术干预的晶状体后球形突出。手术时，变薄且鼓起的后囊破裂。据报道，保守治疗PFV不会导致进行性晶状体后球形突出。本病例记录了PFV与晶状体后球形突出罕见的同时出现情况。
