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起源于神经节神经胶质瘤的前庭性发作和自发性下跳性眼球震颤:病例报告。

Vestibular seizures and spontaneous downbeat nystagmus of ganglioglioma origin: a case report.

机构信息

Department of Otorhinolaryngology - Head and Neck Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, PR China.

出版信息

BMC Neurol. 2023 Jul 24;23(1):278. doi: 10.1186/s12883-023-03311-6.

Abstract

BACKGROUND

Low-grade gangliogliomas (GGs) are typically epileptogenic intracranial neoplasms. Yet, the presentation of simplex vertiginous experience and spontaneous downbeat nystagmus (DBN) has not been reported to date.

CASE PRESENTATION

We present the case of a 26-year-old male with focal onset impaired awareness seizures, characterized by vertigo due to right temporal lobe epilepsy caused by ganglioglioma. As rare presentations, a spontaneous, consistent DBN in the absence of vertiginous experience was noticed. MRI suggested lesion in the right temporal pole. Twenty-four-hour continuous electroencephalogram (EEG) monitoring recorded periodic sharp and slow waves, originating from the right temporal lobe. The patient was completely relieved of the symptoms after surgical removal of the tumor, which was histologically confirmed as Grade I Ganglioglioma.

CONCLUSIONS

Asides from the cortical pathogenesis of epileptic vertigo, this case also provides insight into the DBN secondary to tumor of the temporal lobe. Moreover, the 24-h EEG is advantageous to recognize vestibular seizures and localize the ictal onset areas.

摘要

背景

低级别神经节细胞瘤(GGs)通常是具有致痫性的颅内肿瘤。然而,目前尚未有单纯眩晕发作和自发性下跳性眼球震颤(DBN)的报道。

病例介绍

我们报告了一例 26 岁男性局灶性意识障碍性癫痫发作病例,其病因是右颞叶癫痫,由神经节细胞瘤引起。作为罕见表现,患者出现了无眩晕的自发性、持续性 DBN。MRI 提示病变位于右颞极。24 小时连续脑电图(EEG)监测记录到起源于右颞叶的阵发性尖慢波。肿瘤切除后,患者症状完全缓解,组织学证实为 1 级神经节细胞瘤。

结论

除了癫痫性眩晕的皮质发病机制外,本病例还提示了颞叶肿瘤继发 DBN。此外,24 小时 EEG 有利于识别前庭性癫痫发作和定位发作起始区。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5f/10364402/1f4b2889e639/12883_2023_3311_Fig1_HTML.jpg

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