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Case Report: Unilateral persistent hyperplastic primary vitreous: intensive management approach with excellent outcome beyond visual maturation

机译:病例报告:单侧持续性增生性原发性玻璃体:强化治疗方法,视觉成熟后效果极佳

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摘要

Persistent hyperplastic primary vitreous (PHPV) is an ocular developmental disorder resulting from incomplete apoptosis of the embryonic hyaloid vasculature. Unilateral PHPV is traditionally associated with a poor prognosis because of the challenges associated with managing progressive anisometropic amblyopia. We report a child with unilateral PHPV who underwent cataract extraction, primary posterior capsulotomy with anterior vitrectomy and intraocular lens implantation followed by combined trabeculectomy/trabeculotomy within the first 8 weeks of life. Intensive optometric and orthoptic input was required for many years to manage the increasing anisometropic amblyopia with final visual acuity of 20/40 unaided in the affected eye and without evidence of glaucomatous optic neuropathy. This case illustrates the excellent visual outcome possible in a child with complex, unilateral PHPV using an intensive management approach comprising: early surgical intervention for congenital cataract and secondary glaucoma, meticulous monitoring of refraction, visual acuity and intraocular pressure and motivated parents who engaged in the management.
机译:持久性增生性原发性玻璃体(PHPV)是一种眼发育异常,是由胚胎透明质样脉管系统的不完全凋亡所致。传统上,单侧PHPV由于与进行性屈光参差性弱视相关的挑战而预后不良。我们报道一名单侧PHPV患儿,在其生命的前8周内接受了白内障摘除,原发性后囊切开术,前玻璃体切除术和人工晶状体植入术,然后进行了小梁切除术/小梁切开术联合治疗。多年以来,需要大量的验光和矫形输入来控制屈光参差性弱视,患眼的最终视力为20/40,而没有青光眼性视神经病变的证据。该案例说明了采用强化管理方法的复杂单侧PHPV儿童可能获得的出色视觉效果,包括:对先天性白内障和继发性青光眼的早期外科手术干预,对屈光,视敏度和眼内压的细致监测以及有动机的父母。管理。

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