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Published on: March 12, 2016
Rhegmatogenous retinal detachment associated with primary congenital glaucoma
Shingo Satofuka1, Yutaka Imamura, Susumu Ishida
1Department of Ophthalmology, Keio University School of Medicine, 35-Shinanomachi, Shinjuku-ku, Tokyo, 160-0016, Japan.
International Ophthalmology
|September 28, 2007
Summary
Rhegmatogenous retinal detachment (RRD) is rare in congenital glaucoma (CG) patients. While surgery can reattach the retina, poor visual outcomes are common in these highly myopic eyes.
Area of Science:
- Ophthalmology
- Retinal Surgery
- Glaucoma Research
Background:
- Rhegmatogenous retinal detachment (RRD) is an uncommon complication in patients with a history of congenital glaucoma (CG).
- This study examines three cases of RRD in highly myopic eyes with prior CG surgery.
Observation:
- All patients were male, with ages 14, 43, and 48, presenting with RRD.
- Retinal tears were equatorial, and detachment severity varied from half to total, including proliferative vitreoretinopathy.
Findings:
- Vitrectomy successfully reattached the retinas in all three cases.
- Despite successful reattachment, all patients experienced poor visual acuity post-surgery.
Implications:
- Advanced vitreous liquefaction in highly myopic eyes may precipitate RRD in CG patients.
- Periodic fundus examinations are recommended for CG patients due to potential poor functional recovery after RRD repair.
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