-
Chronic lymphocytic leukemia/small lymphocytic lymphoma
-
Monoclonal B – cell lymphocytosis
-
B – cell prolymphocytic leukemia
-
Splenic marginal zone lymphoma
-
Hairy cell leukemia
-
Splenic B – cell lymphoma/leukemia, unclassifiable
- Splenic diffuse red pulp small B – cell lymphoma
- Hairy cell leukemia – variant
-
Lymphoplasmacytic lymphoma
- Waldenstrӧm macroglobulinemia
-
Monoclonal gammopathy of undetermined significance (MGUS), IgM
-
µ heavy – chain disease
-
γ heavy – chain disease
-
α heavy – chain disease
-
Monoclonal gammopathy of undetermined significance (MGUS), IgG/A
-
Plasma cell myeloma
-
Solitary plasmacytoma of bone
-
Extraosseous plasmacytoma
-
Monoclonal immunoglobulin deposition diseases
-
Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
(MALT lymphoma)
-
Nodal marginal zone lymphoma
- Pediatric nodal marginal zone lymphoma
-
Follicular lymphoma
- In situ follicular neoplasia
- Duodenal – type follicular lymphoma
-
Pediatric – type follicular lymphoma
-
Large B – cell lymphoma with IRF4 rearrangement
-
Primary cutaneous follicle center lymphoma
-
Mantle cell lymphoma
- In situ mantle cell neoplasia
-
Diffuse large B – cell lymphoma (DLBCL), NOS
- Germinal center B – cell type
- Activated B – cell type
-
T – cell/histiocyte – rich large B – cell lymphoma
-
Primary DLBCL of the central nervous system (CNS)
-
Primary cutaneous DLBCL, leg type
-
EBV+ DLBCL, NOS*
-
EBV+ mucocutaneous ulcer
-
DLBCL associated with chronic inflammation
-
Lymphomatoid granulomatosis
-
Primary mediastinal (thymic) large B – cell lymphoma
-
Intravascular large B – cell lymphoma
-
ALK1+ large B – cell lymphoma
-
Plasmablastic lymphoma
-
Primary effusion lymphoma
-
HHV8+ DLBCL, NOS
-
Burkitt lymphoma
-
Burkitt – like lymphoma with 11q aberration
-
High – grade B – cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
-
High – grade B – cell lymphoma, NOS
-
B – cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma