Geographic Atrophy and Calcified Drusen
- Represents the most advanced form of nonneovascular AMD.
- Pathogenesis is unclear, but may raise from:
- Areas of confluent large, soft drusen that undergone regression
- Multiple reticulated areas of hyper- or hypopigmentation (non-geographic atrophy) which may progress to one large area of GA, spreads contiguously around the fovea and eventually surrounding it
- Spontaneous flattening of a pigment epithelial detachment
Clinical Features
- Symptoms:
- Gradual or progressive loss of vision, depending on the extend and the location of the atrophy relative to the foveal center
- Reduced contrast sensitivity
- Signs:
- Single or multiple discrete areas of hypopigmentation or depigmentation or absent of the RPE forming an areolar pattern
- Often appear as bilateral and symmetric disease, although they may have different onset and progression rates
- Visualization of the larger caliber choroidal vessels within the atrophied area
- May be accompanied by calcified drusen which appears as glistening, bright yellow specks
- The areas of atrophy will continue to enlarge over time
Fluorescein angiography findings:
- Early and discrete bright hyperfluorescence
- Slowly or entirely absent of choriocapillaris filling within the GA zone
- Persistent staining of the atrophied area with a maintaining border in the late phase