Abstract
Purpose: To describe the clinical course of patients with punctate inner choroidopathy seen at the University of Illinois, with emphasis on development of choroidal neovascularization (CNV). Methods: Patients with a diagnosis of punctate inner choroidopathy were identified retrospectively. The diagnosis was made clinically based on findings of multiple, small "punched-out" lesions in the posterior pole without intraocular inflammation. Medical records were evaluated for evidence of CNV. Results: Twelve patients with a diagnosis of punctate inner choroidopathy were identified. Average age at presentation was 32 years (range, 24-52 years). Eleven were women, and 11 were white. Eleven patients had available refractive data: 10 were myopic. Eight had CNV at initial presentation, and 1 later developed CNV. Eight had follow-up averaging 4 years (range, 1.4-9.6 years). Of these, five had CNV at initial presentation, and five developed new CNV. Four had multiple CNV membranes. All 6 patients with follow-up of ≥3 years had visual acuity at 3 years postpresentation of >20/40 in at least 1 eye. Four had visual acuity >20/40 bilaterally. Conclusion: Of punctate inner choroidopathy patients in this series, 75% had CNV, and more than 30% developed multiple neovascular membranes. With treatment, all patients with follow-up of ≥3 years had >20/40 vision in at least 1 eye.
Original language | English (US) |
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Pages (from-to) | 1387-1391 |
Number of pages | 5 |
Journal | Retina |
Volume | 31 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2011 |
Keywords
- CNV
- PIC
- choroidal neovascularization
- punctate inner choroidopathy
- recurrence
- uveitis
ASJC Scopus subject areas
- Ophthalmology