J. Gerling et al., VISUAL-FIELD DEFECTS IN OPTIC NEURITIS AND ANTERIOR ISCHEMIC OPTIC NEUROPATHY - DISTINCTIVE FEATURES, Graefe's archive for clinical and experimental ophthalmology, 236(3), 1998, pp. 188-192
Background: We analyzed the value of visual field defects in the diffe
rential diagnosis of optic neuritis (ON) and non-arteritic anterior is
chemic optic neuropathy (AION). Methods: Ninety-nine consecutive patie
nts with acute-onset optic neuropathy formed the basis for this study.
Compressive and vasculitic neuropathies were excluded. Eighty-six pat
ients fulfilled the criteria for either ON (50 patients): less than or
equal to 35 years, normal disk, recovery of visual function, or AION
(36 patients): greater than or equal to 60 years, swelling of the disk
, no recovery of visual function. Without knowledge of other clinical
data, visual fields obtained by Goldmann perimetry were classified int
o five types of defects (forced choice). With the correct diagnosis at
hand, fields were reviewed for characteristic features. Results: Forc
ed-choice classification into defect types [%]: Central scotoma ON 68,
AION 18; superior altitudinal defect ON 13, AION 7; inferior altitudi
nal defect ON 8, AION 52; peripheral defect ON 1, AION 5; diffuse defe
ct ON 10, AION 18. Search for pathognomonic defects: a scotoma centere
d on the fixation point with a sloping border occurred exclusively in
ON (25 of 50 patients). An inferior altitudinal defect with a sharp bo
rder along the horizontal meridian, particularly in the nasal peripher
y, occurred only in AION (10 of 36 patients). A steep centrocecal scot
oma occurred in 3 of the 36 AION cases and not at all in the ON cases.
Scotomas in the center breaking through to the periphery, superior al
titudinal defects (with a sloping border along the horizontal meridian
) and diffuse depressions verging on blindness occurred in both ON and
AION. Conclusion: A scotoma centered on the fixation point with a slo
ping border is highly characteristic of ON, while an inferior altitudi
nal defect with a sharp border along the horizontal meridian, particul
arly in the nasal periphery, is highly characteristic of AION. To iden
tify these diagnostic criteria, it can be necessary to examine full fi
elds. With restriction of perimetry to 30 degrees a large central scot
oma can be mistaken for a diffuse defect and the border in the nasal p
eriphery can be missed.