Williamson P D, Thadani V M, Darcey T M, Spencer D D, Spencer S S, Mattson R H
Department of Neurology, Yale University School of Medicine, New Haven, CT.
Ann Neurol. 1992 Jan;31(1):3-13. doi: 10.1002/ana.410310103.
Twenty-five patients with occipital lobe seizure origin were retrospectively evaluated to determine clinical seizure characteristics and electroencephalographic manifestations. Certain symptoms and signs served to identify occipital lobe origin in 22 (88%). These included elementary visual hallucinations, ictal amaurosis, eye movement sensations, early forced blinking or eyelid flutter, and visual field deficits. Eye or head deviation, or both, was observed frequently and was contralateral to the side of seizure origin in 13, but 3 patients exhibited ipsilateral deviation in some or all their seizures. After the initial signs and symptoms, clinical seizure characteristics resembled those of seizures originating elsewhere. Seizures typical of temporal lobe origin with loss of contact and various types of automatic, semipurposeful activity occurred in 11 patients. Seizures in 3 patients exhibited asymmetrical tonic or focal clonic motor patterns characteristic of frontal lobe seizures. Eleven of the 25 patients had, on two occasions, two or more distinctly different seizure types. Scalp electroencephalographic findings were seldom helpful for occipital lobe localization and were frequently misleading. Intracranial electroencephalographic recording correctly identified occipital lobe seizure origin in most, but not all, patients who had such studies. Intracranial electroencephalic recording also proved the variability in clinical seizure characteristics was related to different seizure spread patterns, medially or laterally above and below the sylvian fissure, both ipsilateral and contralateral to the occipital lobe of seizure origin. Eighteen patients had occipital lobe lesions detected with computed tomographic or magnetic resonance imaging scans or both. Resection of the lesions in 16 patients produced excellent results in 14 (88%). Five patients had temporal lobectomies, with good results in 3, but poor results in 2. Two patients with unlocalized seizures had complete section of the corpus callosum, 1 with a good result and the other with a poor result.
对25例枕叶癫痫起源患者进行回顾性评估,以确定临床癫痫发作特征和脑电图表现。某些症状和体征有助于在22例(88%)患者中识别枕叶起源。这些症状包括基本视幻觉、发作性黑矇、眼球运动感觉、早期强迫眨眼或眼睑颤动以及视野缺损。经常观察到眼球或头部偏斜,或两者皆有,其中13例偏斜与癫痫起源侧对侧,但3例患者在部分或全部发作中表现为同侧偏斜。在初始症状和体征之后,临床癫痫发作特征与起源于其他部位的癫痫发作相似。11例患者出现典型的颞叶起源癫痫发作,伴有意识丧失和各种类型的自动、半目的性活动。3例患者的癫痫发作表现为额叶癫痫特征性的不对称强直或局灶性阵挛运动模式。25例患者中有11例曾两次或两次以上出现明显不同的癫痫发作类型。头皮脑电图检查结果对枕叶定位很少有帮助,且常常产生误导。颅内脑电图记录在大多数(但并非所有)接受此项检查的患者中正确识别了枕叶癫痫起源。颅内脑电图记录还证明,临床癫痫发作特征的变异性与不同的癫痫扩散模式有关,即沿外侧裂上下内侧或外侧扩散,与癫痫起源枕叶同侧和对侧均有关。18例患者通过计算机断层扫描或磁共振成像扫描或两者均检查发现有枕叶病变。16例患者切除病变,其中14例(88%)效果良好。5例患者接受了颞叶切除术,3例效果良好,2例效果不佳。2例癫痫发作部位未明确的患者接受了胼胝体完全切开术,1例效果良好,另1例效果不佳。