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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Bilateral Persistent Hyperplastic Primary Vitreous - A Rare Case Report ND01-ND02
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Bilateral Persistent Hyperplastic Primary Vitreous - A Rare Case Report ND01-ND02

机译：双侧持续性增生性原发性玻璃体-罕见病例报告ND01-ND02

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Persistent Hyperplastic Primary Vitreous (PHPV), now-a-days referred to as Persistent Fetal Vasculature (PFV), is a rare congenital anomaly of the eye that typically presents unilaterally with white pupillary reflex and microphthalmia without systemic associations. Bilateral presentations are rare. Here we report a case of 15-year-old male with bilateral PFV without leucokoria who was misdiagnosed as congenital esotropia with amblyopia, treated for refractive errors and referred to higher centre for squint corrections. The diagnosis of PFV was made easily on slit lamp examination with dilated pupil due to media clarity. Findings were confirmed by colour doppler ultrasonography of the eyes. This case warrants essential screening of the posterior segment of all children with deviated eyes to ensure earliest detection of such pathologies.
机译：持续性增生性原发玻璃体（PHPV），现今称为持续性胎儿脉管系统（PFV），是一种罕见的先天性眼部畸形，通常单侧表现为白色瞳孔反射和微眼，没有系统性关联。双边介绍很少。在这里，我们报道一例15岁的男性，患有双侧PFV且无白细胞减少症，但被误诊为先天性内斜视并伴有弱视，治疗了屈光不正，并转诊至较高的斜视矫正中心。 PFV的诊断很容易在裂隙灯检查中检查，因为介质清晰，瞳孔散大。通过眼睛的彩色多普勒超声检查证实了发现。该病例需要对所有眼斜视儿童的后段进行必要的筛查，以确保尽早发现此类病状。

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