Abstract
Membranoproliferative glomerulonephritis (MPGN) type 2 is characterized by electron-dense deposits in the glomerular basement membrane and drusen-like deposits in Bruch's membrane. Over time, atrophic changes in the retina and retinal pigment epithelium occur, which can progress to choroidal neovascularization (CNV). This report describes a patient with MPGN type 2 who developed progressive loss of vision secondary to CNV. High-speed ultrahigh-resolution optical coherence tomography (UHR-OCT) showed an irregular Bruch's membrane that measured 10 μm beneath the foveal center. High-speed UHR-OCT can potentially be used to analyze Bruch's membrane in secondary ocular manifestations of diseases such as MPGN type 2 and primary retinal diseases such as age-related macular degeneration.
Original language | English (US) |
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Pages (from-to) | 614-617 |
Number of pages | 4 |
Journal | Ophthalmic Surgery Lasers and Imaging Retina |
Volume | 45 |
Issue number | 6 |
DOIs | |
State | Published - Nov 1 2014 |
Externally published | Yes |
ASJC Scopus subject areas
- Surgery
- Ophthalmology