Sarnat Harvey B
Departments of Paediatrics (Neurology), Pathology (Neuropathology) and Clinical Neurosciences, University of Calgary Cumming School of Medicine and Alberta Children's Hospital Research Institute, Calgary, Alberta, Canada.
Handb Clin Neurol. 2018;154:109-128. doi: 10.1016/B978-0-444-63956-1.00007-2.
The cerebellar system is a series of axonal projections and synaptic circuits as networks, similar to those of the limbic system and those subserving the propagation and spread of seizures. Three principal cerebellar networks are identified and cerebellar disease often affects components of the networks other than just the cerebellar cortex. Contemporary developmental neuropathology of the cerebellum is best considered in the context of alterations of developmental processes: embryonic segmentation and genetic gradients along the three axes of the neural tube, individual neuronal and glial cell differentiation, migration, synaptogenesis, and myelination. Precisely timed developmental processes may be delayed or precocious rhombencephalosynapsis and pontocerebellar hypoplasia exemplify opposite gradients in the horizontal axis. Chiari II malformation may be reconsidered as a disorder of segmentation rather than simply due to mechanical forces upon normally developing hindbrain structures. Cellular nodules in the roof of the fourth ventricle are heterotopia of histologically differentiated but architecturally disoriented and disorganized neurons and glial cells; they often are less mature immunocytochemically than similar cells in adjacent normal folia. Cell rests are nodules of undifferentiated neuroepithelial cells. Both are frequent in human fetuses and neonates. Axonal projections from heterotopia to adjacent cerebellar folia or nuclei are few or absent, hence these nodules are clinically silent despite neuronal differentiation.
小脑系统是一系列作为网络的轴突投射和突触回路,类似于边缘系统以及那些与癫痫发作的传播和扩散相关的系统。已确定三个主要的小脑网络,并且小脑疾病通常不仅影响小脑皮质,还会影响这些网络的其他组成部分。小脑的当代发育神经病理学最好在发育过程改变的背景下进行考量:胚胎分割以及沿神经管三个轴的遗传梯度、单个神经元和胶质细胞的分化、迁移、突触形成和髓鞘形成。精确计时的发育过程可能会延迟或早熟,菱脑融合和脑桥小脑发育不全在水平轴上体现了相反的梯度。Chiari II 畸形可能应重新被视为一种分割障碍,而不仅仅是由于对正常发育的后脑结构施加机械力所致。第四脑室顶部的细胞结节是组织学上已分化但结构上定向紊乱且组织混乱的神经元和胶质细胞的异位;它们在免疫细胞化学上通常比相邻正常小叶中的类似细胞成熟度更低。细胞残余是未分化神经上皮细胞的结节。两者在人类胎儿和新生儿中都很常见。从异位到相邻小脑小叶或核的轴突投射很少或不存在,因此尽管神经元已分化,但这些结节在临床上并无症状。