De Rosa M J, Secor D L, Barsom M, Fisher R S, Vinters H V
Department of Pathology (Division of Neuropathology), UCLA Medical Center 90024-1732.
Acta Neuropathol. 1992;84(3):250-60. doi: 10.1007/BF00227817.
Tissues from three cases of hemimegalencephaly (HME) causing intractable seizures treated by cortical resection were studied using immunohistochemical, ultrastructural, and morphometric techniques. Severe cortical dysplasia was seen in all cases and included lesions best characterized as hemilissencephaly and polymicrogyria. Blurring of the cortex-white matter junction, the presence of large neuronal heterotopias, and neuronal cytomegaly were frequent observations. Immunohistochemical analysis demonstrated cellular colocalization of astrocytic markers glial fibrillary acidic protein and vimentin in one case of hemilissencephaly. Morphometric data showed significant increases over controls in neuronal profile area in all cases of HME. Neuronal cell density was increased significantly above controls in one of the cases. The study shows that HME results from severe cortical dysplasia which may be caused by multiple insults, manifest in one of several ways, and reflects abnormal or altered signals that regulate cortical morphogenesis.
运用免疫组织化学、超微结构和形态计量学技术,对3例因难治性癫痫接受皮质切除术治疗的半侧巨脑症(HME)患者的组织进行了研究。所有病例均可见严重的皮质发育异常,包括最典型的半侧无脑回和多小脑回病变。皮质-白质交界处模糊、存在大型神经元异位和神经元细胞肥大是常见表现。免疫组织化学分析显示,在1例半侧无脑回病例中,星形胶质细胞标志物胶质纤维酸性蛋白和波形蛋白存在细胞共定位。形态计量学数据显示,所有HME病例的神经元轮廓面积均显著高于对照组。其中1例病例的神经元细胞密度显著高于对照组。该研究表明,HME是由严重的皮质发育异常引起的,这种异常可能由多种损伤导致,以几种方式之一表现出来,并反映了调节皮质形态发生的异常或改变的信号。