Loddenkemper T, Kellinghaus C, Gandjour J, Nair D R, Najm I M, Bingaman W, Lüders H O
Department of Neurology, The Cleveland Clinic Foundation, Cleveland, OH 44195-5245, USA.
J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):879-83. doi: 10.1136/jnnp.2003.023333.
Piloerection is a rare clinical symptom described during seizures. Previous reports suggested that the temporal lobe is the ictal onset zone in many of these cases. One case series concluded that there is a predominant left hemispheric representation of ictal cold. The aim of this study is to evaluate the localising and lateralising value of pilomotor seizures.
Medical records of patients who underwent video electroencephalogram (EEG) monitoring at the Cleveland Clinic between 1994 and 2001 were reviewed for the presence of ictal piloerection. The clinical history, physical and neurological examination, video EEG data, neuroimaging data, cortical stimulation results, and postoperative follow ups were reviewed and used to define the epileptogenic zone. Additionally, all previously reported cases of ictal piloerection were reviewed.
Fourteen patients with ictal piloerection were identified (0.4%). Twelve out of 14 patients had temporal lobe epilepsy. In seven patients (50%), the ictal onset was located in the left hemisphere. Four out of five patients with unilateral ictal piloerection had ipsilateral temporal lobe epilepsy as compared with the ipsilateral side of pilomotor response. Three patients became seizure free after left temporal lobectomy for at least 12 months of follow up. An ipsilateral left leg pilomotor response with simultaneously recorded after-discharges was elicited in one patient during direct cortical stimulation of the left parahippocampal gyrus.
Ictal piloerection is a rare ictal manifestation that occurs predominantly in patients with temporal lobe epilepsy. Unilateral piloerection is most frequently associated with ipsilateral focal epilepsy. No hemispheric predominance was found in patients with bilateral ictal piloerection.
竖毛是癫痫发作时描述的一种罕见临床症状。既往报道提示,在许多此类病例中颞叶是发作起始区。一个病例系列得出结论,发作期寒战以左侧大脑半球为主。本研究的目的是评估竖毛发作的定位和定侧价值。
回顾1994年至2001年在克利夫兰诊所接受视频脑电图(EEG)监测患者的病历,以确定是否存在发作期竖毛。回顾临床病史、体格和神经系统检查、视频EEG数据、神经影像学数据、皮质刺激结果及术后随访情况,用于确定癫痫灶。此外,还回顾了所有既往报道的发作期竖毛病例。
确定了14例发作期竖毛患者(0.4%)。14例患者中有12例患有颞叶癫痫。7例患者(50%)发作起始位于左侧半球。5例单侧发作期竖毛患者中有4例与竖毛反应同侧的颞叶癫痫。3例患者在接受左侧颞叶切除术后至少随访12个月无癫痫发作。在对1例患者左侧海马旁回进行直接皮质刺激时,引出了同侧左腿竖毛反应并同时记录到放电后电位。
发作期竖毛是一种罕见的发作表现,主要发生于颞叶癫痫患者。单侧竖毛最常与同侧局灶性癫痫相关。双侧发作期竖毛患者未发现半球优势。