Barry E, Sussman N M, Bosley T M, Harner R N
Epilepsia. 1985 Nov-Dec;26(6):577-84. doi: 10.1111/j.1528-1157.1985.tb05694.x.
Five cases of ictal blindness are presented. All are documented to be ictal by simultaneous EEG monitoring during the period of blindness. In three cases, the blindness was complete; in two, it manifested as a homonymous hemianopia. Three cases (including the two with hemianopia) were secondary to vascular lesions; one case was due to a metastatic lesion; and there was one case of idiopathic epilepsy. Age ranged from 13 to 74 years. In all cases, the blindness was reversible with anticonvulsant therapy. All cases but one lasted from hours to days, meeting a criterion of "status epilepticus amauroticus." In the literature, ictal blindness is seldom reported and even less often documented. Unexplained cortical blindness might represent unrecognized seizure activity more often than is appreciated.
本文报告了5例发作性失明病例。所有病例在失明期间均通过同步脑电图监测记录为发作期。3例失明为完全性;2例表现为同向性偏盲。3例(包括2例偏盲患者)继发于血管病变;1例由于转移性病变;1例为特发性癫痫。年龄范围为13至74岁。所有病例中,抗惊厥治疗后失明均可逆。除1例外,所有病例持续数小时至数天,符合“黑蒙性癫痫持续状态”的标准。在文献中,发作性失明很少被报道,记录的就更少了。无法解释的皮质盲可能比人们认识到的更常代表未被识别的癫痫活动。