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. 2018 Aug 21;12:2577–2590. doi: 10.2147/DDDT.S142406

Table 1.

Subtypes of B-NHL in the order of B-cell development

B-cell non-Hodgkin lymphoma (B-NHL) subtype Subgroup Reference Cell of origin
Molecular features
Incidence
B-cell type Localization Translocation Oncogene Per 105 person-years37 % of B-NHL
B-cell acute lymphoblastoid leukemia (B-ALL) 38 Immature BM t(9;22) BCR-ABL 0.8 2.9
Mature Periphery
Mantle-cell lymphoma (MCL) 39 Naïve LN or S t(11;14) Cyclin D1 0.5 2.0
Chronic lymphocytic leukemia (CLL) UM 1 Follicular LN or S ZAP70 5.2 19.8
M Memory
Marginal-zone lymphoma (MZL) 40 Follicular LN or S 1.0 3.7
Follicular lymphoma (FL) 41, 42 Centrocyte GC t(14;18) BCL2 3.2 12.2
Burkitt lymphoma (BL) 43 Follicular GC t(8;14) MYC 0.3 1.1
Diffuse large B-cell lymphoma (DLBCL) GC 44, 45 Centroblast GC PTEN loss 7.1 27.3
ABC Plasmablast GC Mutant CD79, CARD11, MYD88
Waldenström macroglobulinemia (WM) 46 B cells to plasma cells BM MYD88 L265P 0.4 1.3
Multiple myeloma (MM) 47 Plasma cell BM 5.3 20.2

Notes: B-NHL subtypes listed according to development stages of presumed cells of origin; references to recent reviews of diseases included, along with indications of molecular features and incidence.

Abbreviations: ABC, activated B cell; BM, bone marrow; GC, germinal center; LN, lymph node; M, mutated IGHV genes; MZ, marginal zone; S, spleen; UM, unmutated IGHV genes.