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病例报告。一名患有右侧扣带回星形细胞瘤的患者出现痴笑发作。

Case report. Gelastic seizures in a patient with right gyrus cinguli astrocytoma.

作者信息

Nicolae L, Iacob G, Poparda Mihaela, Popescu B O

机构信息

Department of Neurosurgery, University Hospital Bucharest, Romania.

出版信息

J Med Life. 2010 Oct-Dec;3(4):433-6.

Abstract

OBJECTIVE AND IMPORTANCE

Gelastic seizure (GS) also known as "gelastic epilepsy" is a rare type of seizure associated with several different conditions such as tumors--hypothalamic hamartromas, tuberous sclerosis, hemangiomas, post infectious foci, cortical temporal dysplasia. We report one case of this rare condition generated by a right gyrus cinguli gr. II astrocytoma.

CLINICAL PRESENTATION

A 27 year-old male, right handed, was admitted for a 2 years history of very frequent gelastic seizures accompanied sometimes by simple motor partial seizures in both arms, more often being involved his left arm, without impairment of his consciousness state. His neurological examination was normal. Diagnosis was made on native CT scan: minimal hypodense frontal right paramedian lesion, cerebral MRI showed a small well delimited right, parenchymal, homogeneous lesion (16/22/15 mm), involving gyrus cinguli, without perilesional edema and mass effect, hyperintense both on T1 and T2 MR sequences, non-enhancing after Gadolinium. The cerebral lesion was also documented on EEG and video-EEG recordings. Using an interhemispheric microsurgical approach, above the corpus callosum and the right pericallosal artery, at the level of gyrus cinguli, a yellow-gray, infiltrative tumor, having a moderate vascularisation, has been identified and totally removed. The anatomopathological analysis revealed a grade II astrocytoma. The patient recovered very well, without deficits, no gelastic seizures or epileptic manifestations; three months after operation he is still free of seizures.

CONCLUSION

A case of gelastic seizures accompanied by simple motor partial seizures in both arms, without the impairment of his consciousness state induced by a grade II right gyrus cinguli astrocytoma is described and documented by radiological and electrophysiological studies. Using microsurgical resection, the tumor was totally removed, the patient clinical condition improved. Without an affective connotation as in temporal or hypothalamus topography, gelastic seizures are not patognomonic for hypothalamic hamartomas and in the case of frontal localization of the lesion; they can be associated with motor involvement of the limbs as in our case.

摘要

目的及重要性

笑性癫痫(GS)也被称为“笑性癫痫症”,是一种罕见的癫痫类型,与多种不同病症相关,如肿瘤——下丘脑错构瘤、结节性硬化症、血管瘤、感染后病灶、颞叶皮质发育异常。我们报告一例由右侧扣带回第二组星形细胞瘤引发的这种罕见病症。

临床表现

一名27岁右利手男性因有2年频繁笑性癫痫病史入院,有时伴有双臂简单运动性部分性癫痫发作,左臂更常受累,意识状态无损害。其神经系统检查正常。经头颅CT平扫诊断:右侧额叶旁正中极小低密度病灶,脑部MRI显示右侧一个边界清晰的小实质性均匀病灶(16/22/15毫米),累及扣带回,无瘤周水肿及占位效应,在T1和T2 MR序列上均呈高信号,钆增强后无强化。脑电图和视频脑电图记录也记录到了脑部病变。采用经胼胝体上方和右侧胼周动脉的半球间显微手术入路,在扣带回水平,发现并完全切除了一个黄灰色、浸润性、血管化程度中等的肿瘤。病理分析显示为二级星形细胞瘤。患者恢复良好,无功能缺损,无笑性癫痫发作或癫痫表现;术后三个月仍无癫痫发作。

结论

描述了一例由二级右侧扣带回星形细胞瘤引起的伴有双臂简单运动性部分性癫痫发作且意识状态无损害的笑性癫痫病例,并通过放射学和电生理学研究记录在案。通过显微手术切除,肿瘤被完全切除,患者临床状况改善。与颞叶或下丘脑部位不同,笑性癫痫无情感方面的含义,并非下丘脑错构瘤所特有,在病变位于额叶的情况下;它们可如我们病例中那样与肢体运动受累相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fa4/3019062/9300e7bff49d/JMedLife-03-433-g001.jpg

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