PRECURSOR LYMPHOID NEOPLASMS
- B-lymphoblastic leukemia/lymphoma
- B-lymphoblastic leukemia/lymphoma, not otherwise specified
- B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormalities
- B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1
- B-lymphoblastic leukemia/lymphoma with t(v;11q23.3); KMT2A rearranged
- B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1
- B-lymphoblastic leukemia/lymphoma with hyperdiploidy
- B-lymphoblastic leukemia/lymphoma with hypodiploidy
- B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3); IL3-IGH
- B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3); TCF3-PBX1
- B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like (provisional entity)
- B-lymphoblastic leukemia/lymphoma with iAMP21 (provisional entity)
- T-lymphoblastic leukemia/lymphoma
- early T-cell precursor lymphoblastic leukemia (provisional entity)
- natural killer (NK) cell lymphoblastic leukemia/lymphoma (provisional entity)
MATURE B-CELL NEOPLASMS
- 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 (provisional entity)
- hairy cell leukemia-variant (provisional entity)
- lymphoplasmacytic lymphoma
- Waldenström macroglobulinemia
- IgM monoclonal gammopathy of undetermined significance
- heavy-chain diseases
- μ heavy-chain disease
- γ heavy-chain disease
- α heavy-chain disease
- plasma cell neoplasms
- non-IgM monoclonal gammopathy of undetermined significance (IgG/A)
- plasma cell myeloma
- plasma cell myeloma variants
- smoldering (asymptomatic) plasma cell myeloma
- non-secretory myeloma
- plasma cell leukemia
- plasmacytoma
- solitary plasmacytoma of bone
- extraosseous plasmacytoma
- monoclonal immunoglobulin deposition diseases
- primary amyloidosis
- light chain and heavy chain deposition diseases
- plasma cell neoplasms with associated paraneoplastic syndrome
- POEMS syndrome
- TEMPI syndrome
- extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma)
- nodal marginal zone lymphoma
- pediatric nodal marginal zone lymphoma (provisional entity)
- follicular lymphoma
- testicular follicular lymphoma
- in situ follicular neoplasia
- duodenal-type follicular lymphoma
- pediatric-type follicular lymphoma
- large B-cell lymphoma with IRF4 rearrangement (provisional entity)
- primary cutaneous follicle center lymphoma
- mantle cell lymphoma
- leukemic non-nodal mantle cell lymphoma
- in situ mantle cell neoplasia
- diffuse large B-cell lymphoma, not otherwise specified
- germinal center B-cell type
- activated B-cell type
- T-cell/histiocyte-rich large B-cell lymphoma
- primary diffuse large B-cell lymphoma of the central nervous system
- primary cutaneous diffuse large B-cell lymphoma, leg type
- EBV-positive diffuse large B-cell lymphoma, not otherwise specified
- EBV-positive mucocutaneous ulcer (provisional entity)
- diffuse large B-cell lymphoma associated with chronic inflammation
- fibrin-associated diffuse large B-cell lymphoma
- lymphomatoid granulomatosis
- primary mediastinal (thymic) large B-cell lymphoma
- intravascular large B-cell lymphoma
- ALK-positive large B-cell lymphoma
- plasmablastic lymphoma
- primary effusion lymphoma
- HHV8-associated lymphoproliferative disorders
- multicentric Castleman disease
- HHV8-positive diffuse large B-cell lymphoma, not otherwise specified (provisional entity)
- HHV8-positive germinotropic lymphoproliferative disorder
- Burkitt lymphoma
- Burkitt-like lymphoma with 11q aberration (provisional entity)
- high-grade B-cell lymphoma
- high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements
- high-grade B-cell lymphoma, not otherwise specified
- B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma
MATURE T- and NK-CELL NEOPLASMS
- T-cell prolymphocytic leukemia
- T-cell large granular lymphocytic leukemia
- chronic lymphoproliferative disorder of NK cells (provisional entity)
- aggressive NK-cell leukemia
- EBV-positive T-cell and NK-cell lymphoproliferative diseases of childhood
- systemic EBV-positive T-cell lymphoma of childhood
- chronic active EBV infection of T- and NK-cell type, systemic form
- hydroa vacciniforme–like lymphoproliferative disorder
- severe mosquito bite allergy
- adult T-cell leukemia/lymphoma
- extranodal NK-/T-cell lymphoma, nasal type
- intestinal T-cell lymphoma
- enteropathy-associated T-cell lymphoma
- monomorphic epitheliotropic intestinal T-cell lymphoma
- intestinal T-cell lymphoma, not otherwise specified
- indolent T-cell lymphoproliferative disorder of the gastrointestinal tract (provisional entity)
- hepatosplenic T-cell lymphoma
- subcutaneous panniculitis-like T-cell lymphoma
- mycosis fungoides
- Sézary syndrome
- primary cutaneous CD30+ T-cell lymphoproliferative disorders
- lymphomatoid papulosis
- primary cutaneous anaplastic large cell lymphoma
- primary cutaneous peripheral T-cell lymphomas, rare subtypes
- primary cutaneous γδ T-cell lymphoma
- primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma (provisional entity)
- primary cutaneous acral CD8+ T-cell lymphoma (provisional entity)
- primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder (provisional entity)
- peripheral T-cell lymphoma, not otherwise specified
- angioimmunoblastic T-cell lymphoma and other nodal lymphomas of T follicular helper cell origin
- angioimmunoblastic T-cell lymphoma
- follicular T-cell lymphoma (provisional entity)
- nodal peripheral T-cell lymphoma with T follicular helper phenotype (provisional entity)
- anaplastic large-cell lymphoma, ALK-positive
- anaplastic large-cell lymphoma, ALK-negative
- breast implant-associated anaplastic large-cell lymphoma (provisional entity)
HODGKIN LYMPHOMAS
- nodular lymphocyte predominant Hodgkin lymphoma
- classical Hodgkin lymphoma
- nodular sclerosis classical Hodgkin lymphoma
- lymphocyte-rich classical Hodgkin lymphoma
- mixed cellularity classical Hodgkin lymphoma
- lymphocyte-depleted classical Hodgkin lymphoma
IMMUNODEFICIENCY-ASSOCIATED LYMPHOPROLIFERATIVE DISORDERS
- plasmacytic hyperplasia PTLD
- infectious mononucleosis PTLD
- florid follicular hyperplasia PTLD
- polymorphic PTLD
- monomorphic PTLD
- monomorphic B-cell PTLD
- monomorphic T/NK-cell PTLD
- classical Hodgkin lymphoma PTLD
Bibliografía
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J (Eds): WHO CLASSIFICATION OF TUMOURS OF HAEMATOPOIETIC AND LYMPHOID TISSUES (Revised 4th edition). IARC: Lyon 2017