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ACUTE ZONAL OCCULT OUTER RETINOPATHY (AZOOR)

Originally posted on @retina.rocks 11/23/2020

This 20YO female presented with a 5-year history of photopsias in her left eye. Vision was 20/20 bilaterally.

There were subtle pigmentary changes surrounding the left optic nerve (a brighter semicircular lesion in the left nasal macula is an artifact). Fundus autofluorescence shows more dramatic peripapillary changes with outer borders of hyperautofluorescence.

Optical coherence tomography (OCT) shows loss of the photoreceptor bands temporal to the optic nerve. Nasal to the optic nerve, both the photoreceptor bands and retinal pigment epithelium (RPE) are variably disturbed.

An enlarged blind spot is consistent with these peripapillary changes.

Learning Points:
First described by Gass in 1992, acute zonal occult outer retinopathy (AZOOR) initially presents unilaterally or bilaterally in young women with photopsias, central visual changes, and minimal fundoscopic changes.

Zones of visual field loss correspond to the locations of the photopsias. Electroretinography is often abnormal. Some may later develop areas of outer retinal, RPE, and choroidal atrophy in the initially affected retina.

The pathogenesis of the condition remains unclear, but it appears to initially involve inflammation of the photoreceptors. AZOOR is believed to be a part of the spectrum of other ‘photoreceptoritis’ conditions, including multiple evanescent white dot syndrome (MEWDS), acute macular neuroretinitis (AMN), and acute retinal pigment epitheliitis.