Kantzeli Angeliki, Brandt Christian, Tomka-Hoffmeister Maria, Woermann Friedrich, Bien Christian G
Department of Epileptology (Krankenhaus Mara), Bielefeld University, Medical School, Campus Bielefeld-Bethel, Maraweg 21, 33617 Bielefeld, Germany.
Society of Epilepsy Research, Maraweg 21, 33617 Bielefeld, Germany.
Epilepsy Behav Rep. 2021 Dec 8;17:100513. doi: 10.1016/j.ebr.2021.100513. eCollection 2022.
Aphasic status epilepticus (SE) is a rare manifestation of non-convulsive SE (NCSE) and may occasionally be under-recognized. We report a 69-year-old male patient with a pre-existing left parietal oligodendroglioma WHO III after two resections and radio-chemotherapy. The patient was left with some word finding difficulties but had no history of overt seizures. He developed aphasic NCSE, which was only detected by long-term electroencephalography (EEG) monitoring. The 24-hour EEG revealed paroxysmal rhythmic theta-delta activity in left posterior regions that propagated to left temporo-parietal areas. Rhythmic activity appeared every 15-30 min and lasted for 10-110 s. Aphasia was continuously present with superimposed short-lasting clinical deteriorations during the day. Magnetic resonance imaging showed peri-ictal edema on diffusion-weighted images in the insula and fronto-parietal cortex, which supported the diagnosis of SE. NCSE persisted for seven months. The patient recovered upon addition of intravenous phenytoin. One should not only consider aphasic SE when language impairment is episodic, but also when there are prolonged manifestations, especially when the typical differential diagnoses have been excluded. Intravenous therapy may be required to terminate NCSE. With this report, we would like to draw attention to aphasic SE as a rare phenomenon that may be difficult to diagnose and delay management in clinical practice.
失语性癫痫持续状态(SE)是非惊厥性癫痫持续状态(NCSE)的一种罕见表现,可能偶尔未被充分认识。我们报告一例69岁男性患者,既往有左顶叶少突胶质细胞瘤WHO III级,已接受两次手术及放化疗。患者遗留一些找词困难,但无明显癫痫发作史。他发生了失语性NCSE,仅通过长期脑电图(EEG)监测才得以发现。24小时脑电图显示左后区域阵发性节律性θ-δ活动,并扩散至左颞顶区域。节律性活动每15 - 30分钟出现一次,持续10 - 110秒。白天失语持续存在,并伴有短暂的临床症状恶化。磁共振成像显示岛叶和额顶叶皮质在扩散加权图像上有发作期水肿,支持SE的诊断。NCSE持续了七个月。加用静脉注射苯妥英后患者康复。当语言障碍呈发作性时,不仅应考虑失语性SE,当有持续较长时间的表现时也应考虑,尤其是在排除了典型的鉴别诊断之后。可能需要静脉治疗来终止NCSE。通过本报告,我们希望引起对失语性SE这一罕见现象的关注,其在临床实践中可能难以诊断且延误治疗。