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A case of focal epilepsy associated with focal cortical dysplasia and crossed cerebellar diaschisis

机译:与局灶性皮质发育不良和交叉的小脑二硅质骨质相关的局灶性癫痫病例

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We here reported a 24-year-old woman who presented complex partial seizure from 15 years of age. Her brain MRI showed the right perirolandic focal cortical dysplasia (FCD) corresponding to the orofacial division of the primary sensori-motor area. On SPECT (Tc-99 mECD) study, hypoperfusion was demonstrated at the FCD, the right pons and the left cerebellum (crossed cerebellar diaschisis (CCD)). Magnetoencephalography disclosed the current source of the focal spikes was localized on the FCD. To our knowledge, no previous report of a case associated with FCD and CCD was found. We speculated the pathomechanism of the CCD might be related to the persistent epileptogenic firing which inhibited the cerebellar metabolism transsynaptically through cortico (FCD)-ponto-cerebellar pathway.
机译:我们在这里报道了一名24岁的女性,从15岁开始呈现复杂的部分癫痫发作。 她的脑MRI展示了对应于主要感应电机区域的orofacial划分的权利肺部脊髓焦皮质发育不良(FCD)。 在SPECT(TC-99 MECD)的研究中,在FCD,右侧PONS和左心细胞(交叉的小脑二底(CCD))上证明了过低血熔。 磁性脑图公开了焦平峰的电流源在FCD上定位。 据我们所知,未发现与FCD和CCD相关的案件的先前报告。 我们推测CCD的丧失癫痫灭火可能与持续的癫痫发射灭火有关,该灭火抑制通过Cortico(FCD)-Pontbellar途径逐突出的小脑代谢。

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