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. 2023 May 9;108(6):1272–1276. doi: 10.4269/ajtmh.23-0004

Table 2.

Summary of epidemiological, clinical features, neuroimaging findings, histopathological features, and outcome of patients of SSPE with vision loss (N = 96)

Characteristic Value
Age
 Mean, years 17.86
 Median, years 15
 Mode, years 14
 Range, years 2–62
 NA, n 2
Gender
 Female, n (%) 34 (34.4)
 Male, n (%) 60 (62.5)
 NA, n 2
Measles vaccination, n (%)
 Yes 14 (14.6)
 No 14 (14.6)
 NA 68 (70.8)
Childhood measles, n (%)
 Yes 46 (47.9)
 No or NA 14 (14.6)
Geographic areas of reported cases (N = 88), n (%)
 Indian subcontinent 24 (27.2)
 Europe, except Turkey 23 (26.1)
 Turkey 15 (17.0)
 United States and Canada 14 (15.9)
 Japan and Taiwan 6 (6.8)
 Australia 4 (4.5)
 Africa 1 (1.1)
 West Indies 1 (1.1)
Duration of illness, n (%)
 Sudden/acute 14 (14.6)
 ≤ 15 days 28 (29.1)
 16 days–2 months 12 (12.5)
 > 2–6 months 19 (19.8)
 > 6 months–2 years 10 (10.4)
 > 2 years 7 (7.3)
 NA 6 (6.3)
Preceding vision loss, n (%) 73 (76)
Neuroimaging, n
 NA 26
 CT only 8
  Normal 4
  Cerebral atrophy 2
  White-matter hypodensity 2
 MRI
  Normal 9
  T2/FLAIR hypodensity 50
  Cerebral atrophy 1
  Spinal lesions only 1
  Basal ganglion/thalamus involvement 3
  Cortical ribboning 1
  Splenium of the corpus callosum and hippocampus 2
  Disappearing lesions 1
Site of lesion, n (%)
 Retina and choroid 58 (60.4)
 Optic nerve 9 (7.3)
 Cerebral cortex 29 (30.2)
Brain biopsy, n 29
Retinal biopsy, n 7

CT = computed tomography; FLAIR = fluid-attenuated inversion recovery; MRI = magnetic resonance imaging; NA = not available; SSPE = subacute sclerosing panencephalitis.