Table 1.

Clinical characteristics of 6 patients with t(6;14)(p21.1;q32.3)

PatientAge/sexDiagnosisCytogenetics
63/F 1988: AIHA  
  1992: DLBCL 46, XX, 2p−, 6p−, 6q+, 7q−, 9p+, 11q−, 12p+, 13q−,14q+, 20p−  
74/F Leukemic, low-grade B-cell lymphoma, NOS. 46,XX, t(6;14)(p21.1;q32.3), add(6)(q13), del(7)(q33∼34), add(10)(p14), t(14;19)(q32;q13) [4]  
  WBC = 42.5 × 109/L (87% lymphocytes).  46, XX [21] 
  AIHA  
3* 47/M SLVL 46,XY,t(6;14)(p21;q32.3)[11]/46,XY [9]  
68/F SMZL with focal transformation present in intra-abdominal
lymph nodes. 
47,XX,t(6;14)(p21;q32), +12, + add(12)(q22) [9] 
51/M Parotid gland biopsy with background extranodal marginal
zone B-cell lymphoma (MALT) and focal areas of
transformation to DLBCL. 
48,add(X)(p22),Y, del(1)(q21q43), add(2)(p25), +3, del(5)(q13q31), −6, ?add(12)(q24.3),
add(14)(q32), der(14)t(6;14)(p21.1;q32),+18,+mar [9]/47,add(X)(p22), Y, add(1)(q21),
del(1)(q21q43), add(2)(p25), del(5)(q13q31), −6, del(9)(p13), der(14)t(1;14)(q21;q32),
+18, +mar [4]  
42/F Parotid gland biopsy with background extranodal marginal
zone B-cell lymphoma (MALT) and focal areas of
transformation to DLBCL. 
47,X,−X,add(6)(q15),der(14)?t(6;14)(p21.1;q32.3),add(15)(p11),i(18)(q10),add(22)(p11),
+2mar [5]/46,X,−X, ?t(3;14)(p25;q32), der(10)t(10;11)(q26;q13), add(12)(p11),
der(14)?t(6;14)(q32.3;p21.1), add (15)(p11), i(18)(q10), add(22)(p11), + 2mar[3] 
PatientAge/sexDiagnosisCytogenetics
63/F 1988: AIHA  
  1992: DLBCL 46, XX, 2p−, 6p−, 6q+, 7q−, 9p+, 11q−, 12p+, 13q−,14q+, 20p−  
74/F Leukemic, low-grade B-cell lymphoma, NOS. 46,XX, t(6;14)(p21.1;q32.3), add(6)(q13), del(7)(q33∼34), add(10)(p14), t(14;19)(q32;q13) [4]  
  WBC = 42.5 × 109/L (87% lymphocytes).  46, XX [21] 
  AIHA  
3* 47/M SLVL 46,XY,t(6;14)(p21;q32.3)[11]/46,XY [9]  
68/F SMZL with focal transformation present in intra-abdominal
lymph nodes. 
47,XX,t(6;14)(p21;q32), +12, + add(12)(q22) [9] 
51/M Parotid gland biopsy with background extranodal marginal
zone B-cell lymphoma (MALT) and focal areas of
transformation to DLBCL. 
48,add(X)(p22),Y, del(1)(q21q43), add(2)(p25), +3, del(5)(q13q31), −6, ?add(12)(q24.3),
add(14)(q32), der(14)t(6;14)(p21.1;q32),+18,+mar [9]/47,add(X)(p22), Y, add(1)(q21),
del(1)(q21q43), add(2)(p25), del(5)(q13q31), −6, del(9)(p13), der(14)t(1;14)(q21;q32),
+18, +mar [4]  
42/F Parotid gland biopsy with background extranodal marginal
zone B-cell lymphoma (MALT) and focal areas of
transformation to DLBCL. 
47,X,−X,add(6)(q15),der(14)?t(6;14)(p21.1;q32.3),add(15)(p11),i(18)(q10),add(22)(p11),
+2mar [5]/46,X,−X, ?t(3;14)(p25;q32), der(10)t(10;11)(q26;q13), add(12)(p11),
der(14)?t(6;14)(q32.3;p21.1), add (15)(p11), i(18)(q10), add(22)(p11), + 2mar[3] 

AIHA indicates autoimmune hemolytic anemia; NOS, not otherwise specified; WBC, white blood cell count.

*

Patient was a 47-year-old asymptomatic man who was found to have a lymphocytosis, but neither lymphadenopathy nor hepatosplenomegaly, on routine testing. WBC was 30 × 109/L with 73% lymphocytes, whereas bone marrow aspirate contained 80% mature lymphoid cells. Morphology and immunophenotype from blood and marrow were consistent with SLVL, namely, positive staining with CD19, CD20, CD22, CD79a, strong sIgM/Dκ and weak FMC7. CD5 was positive in 39% of cells; CD10 and CD23 were both negative.

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