Aneurysm of the Subclavian Artery and Aneurysm of the Cerebral Artery in Association with Congenital Absence of Ipsilateral Internal Carotid Artery
	    		
	    			
	    			
		        		
			        		
		        		
			        
		   		
		   		
		   			
		   		
	    	
    	 
    	10.4326/jjcvs.35.333
   		
        
        	
        		- VernacularTitle:右内頸動脈無形成に合併した前交通動脈瘤と右鎖骨下動脈瘤の1例
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Fuyuki Asami
			        		
			        		;
		        		
		        		
		        		
			        		Takashi Wakabayashi
			        		
			        		;
		        		
		        		
		        		
			        		Osamu Namura
			        		
			        		;
		        		
		        		
		        		
			        		Masakazu Sogawa
			        		
			        		;
		        		
		        		
		        		
			        		Jun-ichi Hayashi
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            
            	- From:Japanese Journal of Cardiovascular Surgery
	            		
	            		 2006;35(6):333-335
	            	
            	
 
            
            
            	- CountryJapan
 
            
            
            	- Language:Japanese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	A 56-year-old man had aneurysms of the right subclavian artery and cerebral artery in association with congenital absence of the right internal carotid artery. The aneurysm of the subclavian artery was successfully surgically repaired through a partial sternotomy. Congenital absence of the internal carotid artery is rare vascular anomaly. This anomaly contributes to the occurrence of intracranial aneurysms. However, aneurysm of subclavian artery associated with congenital absence of the internal artery is very rare. This is the 3rd case reported in the literature.