Department of Ophthalmology, The Second Hospital of Lanzhou University, Lanzhou, China.
J Int Med Res. 2024 Jan;52(1):3000605231222214. doi: 10.1177/03000605231222214.
Persistent hyperplastic primary vitreous (PHPV) is a rare congenital developmental ocular disorder caused by incomplete regression of the embryonic hyaloid vasculature; bilateral presentations are even rarer. We report a 6-year-old child with bilateral PHPV who visited our hospital for strabismus, without exhibiting leukocoria, microphthalmia, and systemic diseases. These unique characteristics distinguish our case from other cases of PHPV. It is crucial to increase awareness of congenital eye disease in children and the importance of performing fundus examination with the pupils dilated.
永存原始玻璃体增生症(PHPV)是一种罕见的先天性眼部发育异常,由胚胎期玻璃血管系统不完全退化引起;双侧表现更为罕见。我们报告了一例 6 岁儿童,因斜视就诊于我院,无白瞳、小眼球及全身疾病。这些独特的特征使我们的病例与其他 PHPV 病例相区别。提高对儿童先天性眼病的认识,以及散瞳眼底检查的重要性至关重要。