Desmoid Tumor in Familial Adenomatous Polyposis (FAP).
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3393/jksc.2008.24.1.20
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Dae Dong KIM
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Chang Sik YU
			        		
			        		;
		        		
		        		
		        		
			        		Dong Hyun HONG
			        		
			        		;
		        		
		        		
		        		
			        		Sang Hun JUNG
			        		
			        		;
		        		
		        		
		        		
			        		Pyong Wha CHOI
			        		
			        		;
		        		
		        		
		        		
			        		In Ja PARK
			        		
			        		;
		        		
		        		
		        		
			        		Hee Cheol KIM
			        		
			        		;
		        		
		        		
		        		
			        		Jin Cheon KIM
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Colorectal Clinic, Department of Surgery, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea. csyu@amc.seoul.kr
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Original Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Familial adenomatous polyposis;
			        		
			        		
			        		
				        		Desmoid tumor
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Abdominal Wall;
				        		
			        		
				        		
					        		Adenomatous Polyposis Coli;
				        		
			        		
				        		
					        		Fibromatosis, Aggressive;
				        		
			        		
				        		
					        		Humans;
				        		
			        		
				        		
					        		Incidence;
				        		
			        		
				        		
					        		Postoperative Period;
				        		
			        		
				        		
					        		Recurrence
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:Journal of the Korean Society of Coloproctology
	            		
	            		 2008;24(1):20-26
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:Korean
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	PURPOSE: This research was conducted to assess the incidence, clinical characteristics, and treatment outcomes for desmoid tumors in patients with familial adenomatous polyposis (FAP). METHODS: At Medical Center, we recruited 47 patients who had been diagnosed as having intraabdominal or abdominal wall desmoid tumor between Aug. 1995 and Dec. 2005. We compared FAP-associated desmoid tumors with non-FAP-associated desmoid tumors according to clinical characteristics and treatment outcomes. RESULTS: Desmoid tumors developed 12/46 (26.1%) in FAP, 1/14 (7.1%) in attenuated FAP and 34 in non-FAP associated. Unlike non-FAP-associated desmoid tumors, the occurrence of FAP-associated desmoid tumors in tended to be higher in the earlier age groups (< or =40 yrs, 92.3% vs 67.6%, P=0.082) and no sexual predominancy was observed (male:female ratio of 1.2:1 vs a tumor ratio 1:3.9, P=0.033). Intraabdominal-type desmoid tumors associated for the majority of FAP-associated desmoid tumors (92.3% vs 38.2%, P=0.002), and 70% of the desmoid tumors occurred within 3 years after total proctocolectomy. In the treatment of FAP-associated intraabdominal desmoid tumors, surgery was performed in 7 cases (58.3%), and complete resections were done in only 3 cases (25%), with one recurrence. In non-FAP-associated desmoid tumors, complete resection was possible in 10 cases (76.9%), and there was no recurrence (P=0.036). The medical treatment for unresectable or incompletely resectable cases in cases of non-FAP-associated desmoid tumor was good, but for FAP-associated desmoid tumors, the effectiveness was not good, and further investigation was needed. CONCLUSIONS: Intraabdominal desmoid tumors in FAP patients occurred frequently in the early (< or =3 yrs) postoperative period, and the treatment, outcome including surgery and medication, outcome was not good in patients with FAP-associated desmoid tumors.