Table 2.

IgVH mutational frequency considering the productive rearrangement in 96 MCL cases, in relation to the main clinical features at presentation

0%Frequency of IgVHsomatic mutation
More than 0%More than 2%More than 5%
Total 29 67 28 13 
Splenomegaly at diagnosis 5/26 21/26 11/26 5/26  
Splenic primary MCL 1/5 4/5 3/5 3/5* 
PB/BM infiltration 13/51 38/51 17/51 9/51  
I/II CS 4/9 5/9 1/9 1/9 
Waldeyer 1/7 6/7 0/7 0/7 
Intestinal 0/7 7/7 3/7 0/7  
Diffuse/nodular/MZ pattern 6/13/3 20/18/6 8/6/3 2/3/1 
Blastoid 5/14 9/14 6/14 3/14  
i-GC Cyclin D1+ cells 5/20 14/20 6/20 3/20 
0%Frequency of IgVHsomatic mutation
More than 0%More than 2%More than 5%
Total 29 67 28 13 
Splenomegaly at diagnosis 5/26 21/26 11/26 5/26  
Splenic primary MCL 1/5 4/5 3/5 3/5* 
PB/BM infiltration 13/51 38/51 17/51 9/51  
I/II CS 4/9 5/9 1/9 1/9 
Waldeyer 1/7 6/7 0/7 0/7 
Intestinal 0/7 7/7 3/7 0/7  
Diffuse/nodular/MZ pattern 6/13/3 20/18/6 8/6/3 2/3/1 
Blastoid 5/14 9/14 6/14 3/14  
i-GC Cyclin D1+ cells 5/20 14/20 6/20 3/20 

PB indicates peripheral blood; BM, bone marrow; CS, clinical stage; MZ, marginal zone; i-GC, intragerminal center cyclin D1+ cells.

*

P < .05.

P = .069.

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