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新发癫痫持续状态伴孤立性失语。

De novo status epilepticus with isolated aphasia.

作者信息

Flügel Dominique, Kim Olaf Chan-Hi, Felbecker Ansgar, Tettenborn Barbara

机构信息

Department of Neurology, Kantonsspital St. Gallen, Rorschacherstrasse 95, 9000 St. Gallen, Switzerland.

Department of Neuroradiology and Nuclear Medicine, Kantonsspital St. Gallen, Rorschacherstrasse 95, 9000 St. Gallen, Switzerland.

出版信息

Epilepsy Behav. 2015 Aug;49:198-202. doi: 10.1016/j.yebeh.2015.05.009. Epub 2015 Jun 1.

Abstract

BACKGROUND

Sudden onset of aphasia is usually due to stroke. Rapid diagnostic workup is necessary if reperfusion therapy is considered. Ictal aphasia is a rare condition but has to be excluded. Perfusion imaging may differentiate acute ischemia from other causes. In dubious cases, EEG is required but is time-consuming and laborious. We report a case where we considered de novo status epilepticus as a cause of aphasia without any lesion even at follow-up. A 62-year-old right-handed woman presented to the emergency department after nurses found her aphasic. She had undergone operative treatment of varicosis 3 days earlier. Apart from hypertension and obesity, no cardiovascular risk factors and no intake of medication other than paracetamol were reported. Neurological examination revealed global aphasia and right pronation in the upper extremity position test. Computed tomography with angiography and perfusion showed no abnormalities. Electroencephalogram performed after the CT scan showed left-sided slowing with high-voltage rhythmic 2/s delta waves but no clear ictal pattern. Intravenous lorazepam did improve EEG slightly, while aphasia did not change. Lumbar puncture was performed which likely excluded encephalitis. Magnetic resonance imaging showed cortical pathological diffusion imaging (restriction) and cortical hyperperfusion in the left parietal region. Intravenous anticonvulsant therapy under continuous EEG resolved neurological symptoms. The patient was kept on anticonvulsant therapy. Magnetic resonance imaging after 6 months showed no abnormalities along with no clinical abnormalities.

CONCLUSIONS

Magnetic resonance imaging findings were only subtle, and EEG was without clear ictal pattern, so the diagnosis of aphasic status remains with some uncertainty. However, status epilepticus can mimic stroke symptoms and has to be considered in patients with aphasia even when no previous stroke or structural lesions are detectable and EEG shows no epileptic discharges. Epileptic origin is favored when CT or MR imaging reveal no hypoperfusion. In this case, MRI was superior to CT in detecting hyperperfusion. This article is part of a Special Issue entitled "Status Epilepticus".

摘要

背景

失语症的突然发作通常归因于中风。如果考虑进行再灌注治疗,则需要进行快速诊断检查。发作性失语症是一种罕见的病症,但必须排除。灌注成像可以区分急性缺血与其他病因。在可疑病例中,需要进行脑电图检查,但该检查耗时且费力。我们报告了一例病例,即使在随访时也未发现任何病变,但我们认为新发癫痫持续状态是失语症的病因。一名62岁右利手女性在护士发现她失语后被送往急诊科。她3天前接受了静脉曲张手术治疗。除高血压和肥胖外,未报告有心血管危险因素,除对乙酰氨基酚外未服用其他药物。神经系统检查显示完全性失语症,上肢姿势试验显示右侧旋前。计算机断层扫描血管造影和灌注检查未发现异常。CT扫描后进行的脑电图检查显示左侧慢波,伴有2赫兹的高电压节律性δ波,但无明确的发作模式。静脉注射劳拉西泮确实使脑电图略有改善,但失语症未改变。进行了腰椎穿刺,这可能排除了脑炎。磁共振成像显示左侧顶叶区域有皮质病理扩散成像(受限)和皮质高灌注。在持续脑电图监测下进行静脉抗惊厥治疗后,神经症状得到缓解。患者继续接受抗惊厥治疗。6个月后的磁共振成像显示没有异常,临床也无异常。

结论

磁共振成像结果仅为细微表现,脑电图无明确的发作模式,因此失语症状态的诊断仍存在一定不确定性。然而,癫痫持续状态可模仿中风症状,即使在未发现既往中风或结构性病变且脑电图未显示癫痫放电的失语症患者中也必须考虑。当CT或磁共振成像未显示灌注不足时,癫痫起源的可能性较大。在本病例中,磁共振成像在检测高灌注方面优于CT。本文是名为“癫痫持续状态”的特刊的一部分。

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