Case of peripheral fibrovascular proliferative retinopathy associated with morning glory disc anomaly

Tomoka Ishida1, Ryuki Fukumoto1, Yoshihiro Wakabayashi2

  • 1Department of Ophthalmology, Kyorin University, Tokyo, Japan.

Insights

Retinal detachments (RDs) linked to Morning Glory Disc Anomaly (MGDA) are rare. This case highlights a unique tractional RD with massive exudation, successfully treated with vitrectomy and buckling surgery.

Area of Science:

  • Ophthalmology
  • Retinal Diseases
  • Vascular Anomalies

Background:

  • Morning Glory Disc Anomaly (MGDA) is a rare congenital condition affecting the optic nerve head.
  • Retinal detachments (RDs) associated with MGDA typically originate near the optic disc.
  • Peripheral fibrovascular proliferation and tractional RDs are considered uncommon complications of MGDA.

Observation:

  • This report details an unusual case of MGDA with a tractional RD.
  • The patient presented with massive exudation from a peripheral temporal fibrovascular proliferation.
  • Stretched vasculatures due to proliferation and hyaloidal membrane contraction were observed.

Findings:

  • A rare presentation of tractional retinal detachment occurred in an eye with Morning Glory Disc Anomaly.
  • Massive exudation and vascular stretching were key features of this atypical RD.
  • The complex RD was successfully managed surgically.

Implications:

  • This case expands the understanding of potential complications associated with Morning Glory Disc Anomaly.
  • It underscores the importance of considering tractional RD in atypical presentations of MGDA.
  • Successful surgical outcomes demonstrate the efficacy of combined vitrectomy and buckling for complex RDs in MGDA.

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