Recurrent Renal Leiomyosarcoma Mimicking a Colonic Submucosal Tumor: A Case Report.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3393/jksc.2011.27.5.270
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Yun Jeung KIM
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Hee Seok MOON
			        		
			        		;
		        		
		        		
		        		
			        		Eaum Seok LEE
			        		
			        		;
		        		
		        		
		        		
			        		Jae Kyu SUNG
			        		
			        		;
		        		
		        		
		        		
			        		Hyun Yong JEONG
			        		
			        		;
		        		
		        		
		        		
			        		Ji Yeon KIM
			        		
			        		;
		        		
		        		
		        		
			        		Dae Young KANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Internal Medicine, Chungnam National University Hospital, Daejeon, Korea. mhs1357@cnuh.co.kr
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Case Report
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Leiomyosarcoma;
			        		
			        		
			        		
				        		Submucosal tumor;
			        		
			        		
			        		
				        		Recurrence;
			        		
			        		
			        		
				        		Colon;
			        		
			        		
			        		
				        		Kidney
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Abdominal Pain;
				        		
			        		
				        		
					        		Accounting;
				        		
			        		
				        		
					        		Carcinoma, Renal Cell;
				        		
			        		
				        		
					        		Colon;
				        		
			        		
				        		
					        		Colon, Descending;
				        		
			        		
				        		
					        		Colonoscopy;
				        		
			        		
				        		
					        		Female;
				        		
			        		
				        		
					        		Humans;
				        		
			        		
				        		
					        		Kidney;
				        		
			        		
				        		
					        		Leiomyosarcoma;
				        		
			        		
				        		
					        		Middle Aged;
				        		
			        		
				        		
					        		Nephrectomy;
				        		
			        		
				        		
					        		Recurrence
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Journal of the Korean Society of Coloproctology
	            		
	            		 2011;27(5):270-274
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	A primary leiomyosarcoma of the kidney is a rare, but highly aggressive, neoplasm, accounting for only 0.1% of all invasive renal tumors. Local or systemic recurrence is common, but a leiomyosarcoma is difficult to diagnose preoperatively. We recently encountered an interesting case of an unusual recurrence of a renal leiomyosarcoma. A 57-year-old woman visited our hospital complaining of lower abdominal pain. Four years previously, she had undergone a left nephrectomy. She had a primary leiomyosarcoma of the kidney that had been misdiagnosed as a renal cell carcinoma. Colonoscopy revealed the presence of a lesion similar to a submucosal tumor in the descending colon. Postoperative pathologic examination confirmed that the mass was a recurrent leiomyosarcoma. We report this unusual case and present a review of the literature.