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双侧原发性增生性永存玻璃体:两例报告。

Bilateral primary hyperplastic persistent vitreous: report of two cases.

作者信息

Singh Neha, Agrawal Siddharth, Mishra Pallavi

机构信息

Department of Ophthalmology, King George Medical University, Lucknow, Uttar Pradesh, India.

出版信息

GMS Ophthalmol Cases. 2020 Oct 9;10:Doc42. doi: 10.3205/oc000169. eCollection 2020.

Abstract

Primary hyperplastic persistent vitreous (PHPV) or persistent fetal vasculature is a rare clinical entity that presents with leucocoria, microphthalmos, and cataract. It is mostly unilateral. Here we present a report of two cases of bilateral PHPV. One of the patients had associated Peters' anomaly. The entity closely mimics retinoblastoma and should be kept as a differential diagnosis of bilateral leucocoria. Examination under anesthesia, ultrasound B-scan, and aqueous lactate dehydrogenase levels helped us reach the diagnosis and differentiate it from the more serious entity retinoblastoma.

摘要

原发性增生性永存玻璃体(PHPV)或永存胎儿血管系统是一种罕见的临床病症,表现为白瞳症、小眼球和白内障。多数为单侧发病。在此,我们报告两例双侧PHPV病例。其中一名患者合并彼得斯异常。该病症极易与视网膜母细胞瘤混淆,在诊断双侧白瞳症时应将其列为鉴别诊断对象。麻醉下检查、B超扫描及房水乳酸脱氢酶水平检测有助于我们做出诊断,并将其与更严重的视网膜母细胞瘤区分开来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b006/7657025/205ae4505405/OC-10-42-g-001.jpg

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