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顶枕叶胶质增生继发小儿药物难治性癫痫的临床谱

Clinical spectrum of pediatric drug refractory epilepsy secondary to parieto-occipital gliosis.

作者信息

Ray Somdattaa, Kenchaiah Raghavendra, Asranna Ajay, Padmanabha Hansashree, Kulanthaivelu Karthik, Mundlamuri Ravindranadh Chowdary, Viswanathan L G, Chatterjee Aparajita, Thennarasu Kandavel, Sinha Sanjib

机构信息

Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

出版信息

Epilepsy Res. 2021 Dec;178:106804. doi: 10.1016/j.eplepsyres.2021.106804. Epub 2021 Nov 2.

Abstract

BACKGROUND

Parieto-occipital (PO) gliosis secondary to perinatal insult, is often associated with neurologic sequelae such as epilepsy, which can be drug resistant.

OBJECTIVE

To evaluate the spectrum of epilepsy among patients presenting with seizures in association with PO gliosis and to determine factors that influence the development of epileptic encephalopathy (EE) in these patients.

METHODS

We retrospectively evaluated patients aged < 16 years with drug refractory epilepsy and PO gliosis who underwent video electroencephalography (Video EEG). We evaluated the clinical, electrophysiological and radiological profile including treatment responsiveness of subjects with EE.

RESULTS

One hundred one patients (M: F=3:1) with mean age of onset of epilepsy at 28.9 ± 33.1 months were recruited into the study. Based on video EEG findings, Based on video EEG findings, the commonest type of focal onset ictus was tonic seizures with impaired awareness (n = 26, 29.9%). Myoclonic jerks (n = 20, 23%) were the commonest type of generalised onset seizures. Ictal onset from parieto occipital region were observed in 28 patients. Ictal onset from frontal, temporal and fronto temporal region were observed in 6 (6.8%), 7(7.9%) and 9 (8.9%) patients, respectively. Comparison of the seizure types and ictal onset among subgroups of patients with occipital gliosis, parieto-occipital gliosis and parieto-occipital with frontal gliosis revealed that the extent of gliosis did not significantly affect seizure semiology or ictal onset. EE was significantly associated with presence of neonatal seizures (p = 0.04), hypoglycaemia (p = 0.005), longer duration of ICU stay (Z score = -3.55, p < 0.001) and younger age of onset of seizures (Z score = - 2.97, p = 0.03). Eleven out of eighteen (64.7%) subjects with EE showed greater than 50% improvement in seizure frequency following three months of pulse intravenous methylprednisolone therapy.

CONCLUSIONS

Among subjects with PO gliosis on MRI, the seizure semiology is unaffected by laterality, radiologic extension beyond the occipital cortex or presence of ulegyria. Patients with PO gliosis can have florid interictal epileptiform discharges anteriorly and can have seizures with ictal onset from frontal and temporal region. Development of EE is strongly related to the age of onset of seizures, neonatal seizures, prolonged NICU admission, rather than the radiological findings. Subjects with EE and PO gliosis show good response to intravenous pulse methylprednisolone.

摘要

背景

围产期损伤继发的顶枕叶(PO)胶质增生常与癫痫等神经系统后遗症相关,且癫痫可能耐药。

目的

评估伴有PO胶质增生的癫痫患者的癫痫谱,并确定影响这些患者癫痫性脑病(EE)发生发展的因素。

方法

我们回顾性评估了年龄小于16岁、患有药物难治性癫痫和PO胶质增生且接受了视频脑电图(Video EEG)检查的患者。我们评估了包括EE患者治疗反应性在内的临床、电生理和影像学特征。

结果

101例患者(男∶女 = 3∶1)纳入研究,癫痫平均发病年龄为28.9 ± 33.1个月。根据视频脑电图结果,局灶性发作最常见的类型是意识障碍性强直发作(n = 26,29.9%)。肌阵挛性抽搐(n = 20,23%)是全身性发作最常见的类型。28例患者观察到发作起源于顶枕叶区域。分别有6例(6.8%)、7例(7.9%)和9例(8.9%)患者观察到发作起源于额叶、颞叶和额颞叶区域。对枕叶胶质增生、顶枕叶胶质增生和顶枕叶伴额叶胶质增生患者亚组的发作类型和发作起始进行比较,结果显示胶质增生程度并未显著影响发作症状学或发作起始。EE与新生儿惊厥(p = 0.04)、低血糖(p = 0.005)、ICU住院时间延长(Z值 = -3.55,p < 0.001)以及癫痫发作起始年龄较小(Z值 = -2.97,p = 0.03)显著相关。18例EE患者中有11例(64.7%)在接受三个月的静脉注射脉冲甲基强的松龙治疗后癫痫发作频率改善超过50%。

结论

在MRI显示有PO胶质增生的患者中,发作症状学不受病变侧别、枕叶皮质以外的影像学范围或脑回病变的影响。PO胶质增生患者在发作间期可出现明显的前部癫痫样放电,且发作可起源于额叶和颞叶区域。EE的发生发展与癫痫发作起始年龄、新生儿惊厥、NICU住院时间延长密切相关,而非影像学表现。EE和PO胶质增生患者对静脉注射脉冲甲基强的松龙反应良好。

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