Japhet Pobanou Thera*, Tiama JM, Konipo A and Dakouo P
Institute of African Tropical Ophthalmology, Bamako, Mali
*Corresponding Author: Japhet Pobanou Thera, Institute of African Tropical Ophthalmology, Bamako, Mali.
Received: May 14, 2020; Published: June 26, 2020
Purpose: The aim of our study was to report a rare case of persistent hyperplastic primary vitreous.
Case Report: A 4-year-old girl was brought by her parents for impaired visual acuity. The examination of the lens found a tiny opacification. Fundoscopy revealed a membranous proliferation extending from the papilla to the posterior surface of the lens.
Discussion: The persistent primary vitreous is a congenital abnormality. It is due to a failure of regression of the embryonic vitreous to which is added the persistence of the hyoid artery. It occurs around the 6th week of embryo development.
Conclusion: Persistent hyperplastic primary vitreous (PHPV) is a rare congenital anomaly. It has many forms. The Posterior form and the isolated bilateral one is rare.
Keywords: Persistent Primary Vitreous; Posterior; Bilateral
Citation: Japhet Pobanou Thera.,et al. “A Rare Case Report of the Posterior and Bilateral Persistent Hyperplastic Primary Vitreous (PHPV)”Acta Scientific Ophthalmology 3.7 (2020): 45-47.
Copyright: © 2020 Japhet Pobanou Thera.,et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.