Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia. - Suppr | 超能文献

Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia.

作者信息

Cañizares B, Yago I, Piñero Á, Ruiz M

机构信息

Unidad de Oftalmología Infantil, Servicio de Oftalmología, Hospital Virgen de la Arrixaca, Murcia, España.

Unidad de Oftalmología Infantil, Servicio de Oftalmología, Hospital Virgen de la Arrixaca, Murcia, España.

出版信息

Arch Soc Esp Oftalmol. 2017 Jan;92(1):40-43. doi: 10.1016/j.oftal.2016.03.021. Epub 2016 May 24.

DOI:10.1016/j.oftal.2016.03.021

Abstract

CASE REPORT

A case is presented of a 4 week-old female neonate with Peters anomaly (PA) and unilateral persistent foetal vasculature (PFV) referred to our centre due to esotropia. At 12 weeks of age, a penetrating keratoplasty and vitrectomy were performed without major complications in the immediate post-operative period. The patient is currently under an intensive treatment for amblyopia and secondary glaucoma.

DISCUSSION

Surgical treatment of PFV is controversial, with prevention of amblyopia, phthisis, and glaucoma being the main reasons for it. Patients with unilateral PFV and type II PA could be good candidates for this combined surgical procedure.

摘要

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