H. Chuman et al., Atypical Leber's hereditary optic neuropathy: a case with five different episodes of visual disturbance, NEURO-OPHTH, 22(3), 1999, pp. 195-198
We report an unusual case of Leber's hereditary optic neuropathy (LHON) wit
h recurrent episodes of visual disturbance. The patient, a 53-year-old male
, was a heavy smoker and alcohol drinker. At the age of 38, he was diagnose
d as having bilateral optic neuropathy. After corticosteroid therapy, visua
l function recovered. By the age of 40, this condition had recurred five ti
mes. At the age of 51, he demonstrated decreased visual acuity in both eyes
and Goldmann perimetry revealed bilateral cecocentral scotoma. Both optic
nerves had blurred margins, a hyperemic appearance, and microangiopathy. A
peripheral blood specimen showed a point mutation in mitochondrial DNA at n
p11778, indicating LHON. The patient was hospitalized for corticosteroid (m
ethylprednisolone) therapy to help him cease smoking and drinking alcohol.
After this treatment, his visual acuity recovered. We speculate that the me
chanism involved the ATP deficiency theory in which visual disturbance is c
aused by an ATP deficiency due to a gene defect. The induced stress caused
by smoking and drinking diminished during hospitalization due to the cessat
ion of these activities by the patient.