Table 1

Histopathology, immunohistochemistry, and genetics of BL, DLBCL, and B-UNC/BL/DLBCL

BLDLBCLB-UNC/BL/DLBCL
Histopathology Medium-sized and highly monomorphic cells; multiple prominent nucleoli; basophilic cytoplasm; prominent cytoplasmic vacuoles. Heterogeneous with larger cells; vesicular chromatin; multiple peripheral nucleoli; narrow rim of basophilic cytoplasm. Intermediate to large neoplastic cells but monomorphic. 
Interspersed benign histiocytes (classic “starry sky” appearance).   
Ki67 index >95%. Ki67 variable but usually <90%. Ki67 intermediate between BL and DLBCL but high (∼90%). 
Immunohistochemistry CD19, CD20, CD22, CD79a, CD10, BCL6, HLA-DR, and CD43 positive. CD19, CD20, CD22, and CD79a positive. CD19, CD20, CD33, CD79a positive. 
 BCL6 positive 60%-70% of time. BCL6 variable but often positive. 
BCL-2, CD5, TdT, and CD23 negative. BCL2, CD10, CD5, CD30 and CD5 variable. Uniformly CD10 positive. 
  Commonly BCL2 positive. 
Genetics t(8;14) 80%;
t(2;8) 15%;
t(8;22) 5% 
No single cytogenetic change that is typical. “Double hit” cytogenetics with coincident translocations involving MYC and another locus, most often BCL2 30%-50%. 
No translocation involving BCL6 or BCL2. “Double hit” cytogenetics with coincident translocations involving MYC and another locus, most often BCL2 10%. 
BLDLBCLB-UNC/BL/DLBCL
Histopathology Medium-sized and highly monomorphic cells; multiple prominent nucleoli; basophilic cytoplasm; prominent cytoplasmic vacuoles. Heterogeneous with larger cells; vesicular chromatin; multiple peripheral nucleoli; narrow rim of basophilic cytoplasm. Intermediate to large neoplastic cells but monomorphic. 
Interspersed benign histiocytes (classic “starry sky” appearance).   
Ki67 index >95%. Ki67 variable but usually <90%. Ki67 intermediate between BL and DLBCL but high (∼90%). 
Immunohistochemistry CD19, CD20, CD22, CD79a, CD10, BCL6, HLA-DR, and CD43 positive. CD19, CD20, CD22, and CD79a positive. CD19, CD20, CD33, CD79a positive. 
 BCL6 positive 60%-70% of time. BCL6 variable but often positive. 
BCL-2, CD5, TdT, and CD23 negative. BCL2, CD10, CD5, CD30 and CD5 variable. Uniformly CD10 positive. 
  Commonly BCL2 positive. 
Genetics t(8;14) 80%;
t(2;8) 15%;
t(8;22) 5% 
No single cytogenetic change that is typical. “Double hit” cytogenetics with coincident translocations involving MYC and another locus, most often BCL2 30%-50%. 
No translocation involving BCL6 or BCL2. “Double hit” cytogenetics with coincident translocations involving MYC and another locus, most often BCL2 10%. 

B-UNC/BL/DLBCL, B-cell lymphoma unclassifiable with features intermediate between BL and DLBCL.

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