Table 1

Differential diagnosis of white dot syndromes

Sex
age
laterality
Precipitants
onset
duration
prognosis
SymptomsExamination
Multiple evanescent white dot syndromeF>M
3rd–6th decade
Usually unilateral
Viral prodrome
Quick onset
Weeks/months
Very good
Blurred vision
Scotomata
Photopsia
Dyschromatopsia
Blind spot enlarged
Multiple white dots, may coalesce, centred around macula and vascular arcades, granularity at fovea
±vitreous cells
Acute posterior multifocal placoid pigment epitheliopathyM=F
3rd–4th decade
Bilateral
Good
±viral prodrome
Acute
Weeks/months
Good, may be left with mottling
Blurred vision
Scotomata
Photopsia
Yellow/white placoid lesions at posterior pole
±vitreous cells
Acute retinal pigment epitheliitis/Krill diseaseM=F
2nd–4th decade
Usually unilateral
±viral prodrome
Sudden
Weeks–months
Excellent; can recur
Reduced acuity
Metamorphopsia
Scotomata
Small dark hyperpigmented lesions
±few vitreous cells
Punctate inner choroiditisF>M
3rd–4th decade
Bilateral
None
Sudden

Good; may develop chorioretinal scars, choroidal neovascularisation or subretinal fibrosis
Reduced central acuity
Scotomata
Photopsia
Grey/yellow round opacities at posterior pole
No vitreous cells
Acute zonal occult outer retinopathyF>M
Young
Bilateral
±viral prodrome
Sudden
Chronic
Good, but recurrent
Blurred vision
Field defects
Photopsia
White vision
Normal/mottling/retinitis pigmentosa appearance
±vitreous cells
Multifocal choroiditis and panuveitisF>M
3rd–7th decade
Bilateral
±viral prodrome
Insidious
Chronic
Usually poor with scarring
Blurred vision
Scotomata
Photopsia floaters
Myopia
50% iritis, yellow/white lesions →punched out scars
±disc swelling
Birdshot retinochoroidopathy/vitiliginous chorioretinitisF>M
5th–7th decade
Bilateral
None
Insidious
Chronic
Variable cystoid macular oedema can occur, rarely choroidal neovascularisation
Blurred vision
Floaters
Poor night/colour vision
Photopsia
Cream-coloured lesions with patchy depigmentation, optic atrophy, disc swelling
Moderate vitreous cells
Subretinal fibrosis and uveitis syndromeF>M
2nd–4th decade
Bilateral
None
Acute
Chronic
Reduced visionLow vision
Anterior chamber and vitreous inflammation
Serpiginous choroidopathyM>F
4th–7th decade
None
Bilateral
None
Variable
Chronic
Blurred vision
Central/paracentral Scotomata
Photopsia
Geographic areas of grey/yellow discolouration in peripapillary/macula area
±mild vitreous cells
  • Adapted from Crawford and Igboeli.15

  • F, female; M, male.