Käsmann B, Ruprecht K W
Department of Ophthalmology, University of Saarland, Homburg/Saar, Germany.
Ger J Ophthalmol. 1995 Jul;4(4):234-8.
Cortical blindness is defined as a loss of vision due to bilateral retrogeniculate lesions (geniculocalcarine blindness). Gerstmann's syndrome is a combination of disorientation for left and right, finger agnosia, and profound agraphia, alexia, and acalculia. It is due to a lesion in the left angular gyrus, situated at the confluence of the temporal, parietal, and occipital lobes. We report on a patient who suffered from severe underdiagnosed eclampsia and who developed bilateral extensive medial temporal, parietal, and calcarine ischemic infarctions during an eclamptic fit. In addition, ischemia destroyed the left angular gyrus. The combination of these lesions led to Gerstmann's syndrome with additional cortical agnosia and cortical diplopia. For the first few months following the ischemic insult, the patient had been cortically blind. Thereafter, the patient slowly regained a visual acuity of 0.1 in both eyes. She then experienced monocular and binocular diplopia. Her ocular motility was normal; there was no phoria or tropia. Monocular and binocular diplopia slowly became less severe over the following year. Now, 2 years after the incident, the patient has a visual acuity of 0.2 in both eyes and no double vision. However, the handicapping symptoms of Gerstmann's syndrome, which make leading a normal life impossible, have persisted--the patient still cannot cope alone, mainly due to the severe disorientation for left and right. The picture of cortical agnosia, cortical diplopia, and Gerstmann's syndrome is a very rare combination. Visual recovery and rehabilitation in cortical blindness are severely affected and made difficult by the symptoms of Gerstmann's syndrome. In our case the reason for such a dramatic clinical picture was eclampsia, whose prodomes had not been diagnosed in time.
皮质盲被定义为由于双侧膝状体后病变(膝距束性盲)导致的视力丧失。格斯特曼综合征是左右定向障碍、手指失认症以及严重的失写症、失读症和失算症的组合。它是由位于颞叶、顶叶和枕叶交汇处的左侧角回病变引起的。我们报告了一名患有严重未被诊断出的子痫的患者,该患者在子痫发作期间出现了双侧广泛的内侧颞叶、顶叶和距状缺血性梗死。此外,缺血破坏了左侧角回。这些病变的组合导致了伴有额外皮质失认症和皮质性复视的格斯特曼综合征。在缺血性损伤后的最初几个月里,患者处于皮质盲状态。此后,患者双眼视力缓慢恢复到0.1。然后她出现了单眼和双眼复视。她的眼球运动正常;没有隐斜或斜视。在接下来的一年里,单眼和双眼复视逐渐减轻。现在,事件发生2年后,患者双眼视力为0.2,没有复视。然而,格斯特曼综合征的致残症状使正常生活变得不可能,这些症状仍然存在——患者仍然无法独自应对,主要是由于严重的左右定向障碍。皮质失认症、皮质性复视和格斯特曼综合征的情况是一种非常罕见的组合。皮质盲的视觉恢复和康复受到格斯特曼综合征症状的严重影响且变得困难。在我们的病例中,出现这种戏剧性临床表现的原因是子痫,其前驱症状没有及时被诊断出来。