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Cerebellar gangliocytoma presenting with hemifacial spasms: clinical report, literature review and possible mechanisms

机译:小脑神经节细胞瘤伴面肌痉挛:临床报告,文献综述和可能的机制。

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摘要

Cerebellar lesions have classically been considered not to cause epilepsy. However, previous reports have attributed seizures, beginning as hemifacial spasms to lesions of the cerebellar peduncles. We report an example of paroxysmal facial contractions associated with a cerebellar gangliocytoma. The seizures began on the first day of life and consisted of paroxysmal contractions involving the left orbicularis oculi, often the left forehead and lower facial muscles, sometimes accompanied by nystagmoid eye movements to the right and by head deviation to the left. Video-EEG monitoring showed only artifacts from muscle contractions. Magnetic resonance imaging showed a mass arising from the left superior cerebellar peduncle and partially occupying the fourth ventricle. The lesion was removed subtotally and partial seizure control was achieved. The neuropathological findings were consistent with a gangliocytoma. The literature in the association of cerebellar lesions with hemifacial spasms is reviewed and its possible mechanisms discussed.
机译:传统上认为小脑病变不会引起癫痫。然而,先前的报道将癫痫发作归因于癫痫发作,其始于面肌痉挛是小脑梗的病变。我们报告与小脑神经节细胞瘤相关的阵发性面部收缩的例子。癫痫发作始于生命的第一天,包括阵发性收缩,累及左眼轮匝肌,常为左额头和下颌面部肌肉,有时伴有眼球震颤眼球向右运动,头部偏向左侧。视频脑电图监测仅显示来自肌肉收缩的伪影。磁共振成像显示肿块由左上小脑梗引起,并部分占据第四脑室。皮下切除病变,实现部分发作控制。神经病理学结果与神经节细胞瘤一致。综述了小脑病变与面肌痉挛的相关文献,并探讨了其可能的机制。

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