Congenital corneal blood staining secondary to hemorrhagic persistent fetal vasculature

J AAPOS. 2020 Feb;24(1):51-53. doi: 10.1016/j.jaapos.2019.11.007. Epub 2020 Jan 11.

Abstract

An African American girl born at 37 weeks via spontaneous vaginal delivery to a 33-year-old woman was noted on delivery to have a unilateral absent red reflex in the right eye, which was enlarged. Intraocular pressure was elevated, and the cornea had a straw-colored opacity. B-scan ultrasonography of the right eye showed diffuse hyperechoic vitreous opacities and a retrolental mass, with a hyperechoic band stretching from the optic disk to the posterior lens. Neuroimaging showed a unilateral enlarged globe, intraocular hemorrhage, and persistent fetal vasculature, with no other intracranial pathology. An anterior chamber washout revealed liquified blood; the presence of corneal blood staining was confirmed. A spontaneous intraocular hemorrhage associated with persistent fetal vasculature was suspected, leading to secondary glaucoma and corneal blood staining.

Publication types

  • Case Reports

MeSH terms

  • Cornea / blood supply*
  • Cornea / diagnostic imaging
  • Corneal Diseases / diagnosis
  • Corneal Diseases / etiology*
  • Eye Hemorrhage / diagnosis
  • Eye Hemorrhage / etiology*
  • Female
  • Humans
  • Infant, Newborn
  • Intraocular Pressure / physiology*
  • Magnetic Resonance Imaging
  • Persistent Hyperplastic Primary Vitreous / complications*
  • Persistent Hyperplastic Primary Vitreous / diagnosis
  • Ultrasonography