Girotti F, Milanese C, Casazza M, Allegranza A, Corridori F, Avanzini G
Cortex. 1982 Dec;18(4):603-14. doi: 10.1016/s0010-9452(82)80057-9.
A 67-year-old man had repeated cerebral ischemic attacks, which resulted in a clinical picture combining paralysis of visual fixation, optic ataxia and impairment of visuospatial orientation, consistent with the definition of Balint's syndrome. Postmortem examination showed multiple lesions involving the occipital cortex of both sides and the white matter underlying the right insular cortex. EOG recording demonstrated a marked impairment of refixation saccades and saccades on verbal command. Smooth pursuit movements were completely abolished. Visual fixation was randomly achieved after many erratic exploratory movements and steadily maintained on the target (spasmodic fixation). During spasmodic fixation, EOG recording detected an ocular flicker resulting in a continuous instability of eye position. It is suggested that these findings may all be accounted for by the loss of panoramic vision due to a bilateral impairment of cortical areas 18 and 19.
一名67岁男性反复发生脑缺血发作,导致出现一种临床表现,即视觉注视麻痹、视觉性共济失调和视觉空间定向障碍并存,符合巴林特综合征的定义。尸检显示双侧枕叶皮质及右侧岛叶皮质下白质有多处病变。眼电图记录显示,重新注视扫视和听指令扫视明显受损。平稳跟踪运动完全消失。经过多次不稳定的探索性运动后,随机实现了视觉注视,并稳定地保持在目标上(痉挛性注视)。在痉挛性注视期间,眼电图记录检测到眼球闪烁,导致眼位持续不稳定。提示这些发现可能均由双侧18区和19区皮质受损导致全景视觉丧失所致。