A Case of Adult B Lymphoblastic Leukemia with ider(9)(q10)t(9;22)(q34;q11.2) and der(19)t(1;19)(q23;p13.3).
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3343/kjlm.2010.30.6.585
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Soon Il JUNG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Hee Soon CHO
			        		
			        		;
		        		
		        		
		        		
			        		Chae Hoon LEE
			        		
			        		;
		        		
		        		
		        		
			        		Bo Chan JUNG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Laboratory Medicine, Yeungnam University College of Medicine, Daegu, Korea. chscp@ynu.ac.kr
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Case Report ; Research Support, Non-U.S. Gov't
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Recurrent cytogenetic abnormalities;
			        		
			        		
			        		
				        		B lymphoblastic leukemia;
			        		
			        		
			        		
				        		ider(9)(q10)t(9;
			        		
			        		
			        		
				        		22);
			        		
			        		
			        		
				        		der(19)t(1;
			        		
			        		
			        		
				        		19)
			        		
			        		
	        			
        			
        		
 
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Bone Marrow Cells/cytology/pathology;
				        		
			        		
				        		
					        		Chromosome Deletion;
				        		
			        		
				        		
					        		Chromosomes, Human, Pair 1;
				        		
			        		
				        		
					        		Chromosomes, Human, Pair 19;
				        		
			        		
				        		
					        		Chromosomes, Human, Pair 22;
				        		
			        		
				        		
					        		Chromosomes, Human, Pair 9;
				        		
			        		
				        		
					        		Female;
				        		
			        		
				        		
					        		Fusion Proteins, bcr-abl/genetics/metabolism;
				        		
			        		
				        		
					        		Humans;
				        		
			        		
				        		
					        		In Situ Hybridization, Fluorescence;
				        		
			        		
				        		
					        		Karyotyping;
				        		
			        		
				        		
					        		Middle Aged;
				        		
			        		
				        		
					        		Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/*diagnosis/genetics;
				        		
			        		
				        		
					        		*Translocation, Genetic
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:The Korean Journal of Laboratory Medicine
	            		
	            		 2010;30(6):585-590
	            	
            	
 
            
            
            	- CountryRepublic of Korea
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	In B lymphoblastic leukemia/lymphoma (B-ALL/LBL), t(9;22)(q34;q11.2) and t(1;19)(q23;p13.3) are recurrent cytogenetic abnormalities. The concurrent occurrence of both abnormalities is very rare, and only 3 cases have been previously reported. Here, we report a case of adult B-ALL with ider(9)(q10)t(9;22)(q34;q11.2) and der(19)t(1;19)(q23;p13.3). A literature review revealed that ider(9) (q10)t(9;22) is a rare variant of t(9;22) with a deletion of the short arm of chromosome 9. Fifteen cases of ider(9)(q10)t(9;22) have been reported. This abnormality is specific to precursor B-lymphoid neoplasms, such as B-ALL or B-lymphoid blast phase of CML, and is associated with disease progression or short survival. The cytogenetic abnormality t(1;19) is also specific to B-ALL. In most instances of t(1;19), TCF3 is fused to PBX1; however, a few cases have identical translocations but no TCF3-PBX1 fusion, as was observed in our patient. We describe the first case of ider(9)(q10)t(9;22) in combination with TCF3-PBX1 negative t(1;19). The patient underwent imatinib therapy in addition to intensive chemotherapy, but failed to achieve remission.