Dysplasia Type Ia, Ib and Hippocampal Sclerosis: Is Reelin the Missing Link?

R. Andrade-Machado, P. Aguledo-Flórez, L. Salazar-Peláez
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引用次数: 1

Abstract

Abnormal radial and/or tangential cortical lamination in the temporal lobe cortex associated to Hippocampal Sclerosis (HS) is now classified as focal cortical dysplasia (FCD) type IIIa in the current ILAE FCD classification. In these cases, the temporal cortex may show architectural abnormalities or hypertrophic neurons outside layer V. Five variants of FCD type IIIa have been recognized: HS with architectural abnormalities in the temporal lobe; HS with Temporal Lobe Sclerosis (TLS), HS with TLS and heterotopic neurons in subcortical white matter, HS with TLS and small “lentiform” heterotopias in subcortical white matter; and HS without TLS but with small “lentiform” subcortical heterotopias [1]. One of these types of histological features is frequently found in specimens of patients with temporal lobe epilepsy.
Ia型、Ib型发育不良与海马硬化:Reelin是缺失的环节吗?
在当前的ILAE FCD分类中,与海马硬化症(HS)相关的颞叶皮层径向和/或切向皮层层压异常被归类为局灶性皮质发育不良(FCD) IIIa型。在这些病例中,颞叶皮层可能表现为结构异常或v层外神经元肥大。FCD的五种变体IIIa型已被确认:HS伴颞叶结构异常;HS合并颞叶硬化(TLS)、HS合并颞叶硬化并发皮层下白质异位神经元、HS合并颞叶硬化并发皮层下白质小“透镜状”异位神经元;HS无TLS,但有小的“透镜状”皮质下异位[1]。在颞叶癫痫患者的标本中经常发现这些类型的组织学特征之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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