Acta Scientific Ophthalmology (ASOP)

Case Report Volume 3 Issue 7

A Rare Case Report of the Posterior and Bilateral Persistent Hyperplastic Primary Vitreous (PHPV)

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

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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

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References

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Citation

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.




Metrics

Acceptance rate35%
Acceptance to publication20-30 days
ISI- IF1.042
JCR- IF0.24

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