Piloerection as the sole symptom of epilepsy: A case report and review of literature
	    		
		   		
	    	
    	
    	
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Ji-Qing QIU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yu CUI
			        		
			        		;
		        		
		        		
		        		
			        		Li-Chao SUN
			        		
			        		;
		        		
		        		
		        		
			        		Bin QI
			        		
			        		;
		        		
		        		
		        		
			        		Xiao-Bo ZHU
			        		
			        		;
		        		
		        		
		        		
			        		Zhan-Peng ZHU
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Neurosurgery, The First Hospital of Jilin University, 71 Xinmin Street, Changchun, Jilin 130021, P.R. China
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Case report
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Piloerection;
			        		
			        		
			        		
				        		seizure;
			        		
			        		
			        		
				        		EEG
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:Neurology Asia
	            		
	            		 2018;23(2):163-175
	            	
            	
 
            
            
            	- CountryMalaysia
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Piloerection  is  an  involuntary  erection  of  body  hairs  that  usually  has  physiological  correlates  such as  cold  or  a strong  emotional  experience.  Piloerection  may  also  be  a  rare  manifestation  of  seizure.Here,  we  report  a  case  of  54-year-old  man  who  experienced  pilomotor  seizures  from  temporal  lobe  epilepsy. The patient presented with sudden piloerection and no loss of consciousness many times a day. Magnetic resonance imagingof the brain showed threelesions in the right hemisphere, with the largest  lesion  in  the  right  temporal  lobe.  A  video-EEG  showed  an  ictal  discharge  in  the  delta range with right temporal onset. Digital subtraction angiography excluded arteriovenous malformation. The lesion in the right temporal lobe was resected. Immunohistochemistry confirmed a cerebral cavernous malformation.  There  was  no  further  seizure.  A  review  of  the  published  literature  revealed  that  ictal  piloerection as a lone manifestation is rare. Most cases of pilomotor seizure originate in the temporal lobe. Close to four fifth of the cases has a structural lesion. EEG was able to confirm the diagnosis of ictal piloerection in the majority of cases.