Cancer Types: Difference between revisions
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== WHO Classification of Tumours of the Digestive System (2010) == | == WHO Classification of Tumours of the Digestive System (2010) == | ||
== WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (2008) == | == WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (2008) == | ||
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'''Myeloproliferative neoplasms''' | |||
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:Chronic myelogenous leukaemia, BCR-ABL1 positive | |||
:Chronic neutrophilic leukaemia | |||
:Polycythaemia vera | |||
:Primary myelofibrosis | |||
:Essential thrombocythaemia | |||
:Chronic eosinophilic leukaemia, NOS | |||
:Mastocytosis | |||
:Cutaneous mastocytosis | |||
:Systemic mastocytosis | |||
:Mast cell leukaemia | |||
:Mast cell sarcoma | |||
:Extracutaneous mastocytoma | |||
:Myeloproliferative neoplasm, unclassifiable | |||
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'''Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA,PDGFRB or FGFR1''' | |||
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'''Myelodysplastic/myeloproliferative neoplasms''' | |||
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:Chronic myelomonocytic leukaemia | |||
:Atypical chronic myeloid leukaemia, BCR-ABL1 negative | |||
:Juvenile myelomonocytic leukaemia | |||
:Myelodysplastic/myeloproliferative neoplasm, unclassifiable | |||
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'''Myelodysplastic syndromes''' | |||
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:Myelodysplastic syndromes/neoplasms, overview | |||
:Refractory cytopenia with unilineage dysplasia | |||
:Refractory anaemia with ring sideroblasts | |||
:Refractory cytopenia with multilineage dysplasia | |||
:Refractory anaemia with excess blasts | |||
:Myelodysplastic syndrome with isolated del(5q) | |||
:Myelodysplastic syndrome, unclassifiable | |||
:Childhood myelodysplastic syndrome | |||
:Refractory cytopenia of childhood | |||
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'''Acute myeloid leukaemia (AML) and related precursor neoplasms''' | |||
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:AML with recurrent genetic abnormalities | |||
:AML with t(8;21)(q22;q22); RUNX1-RUNX1T1 | |||
:AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 | |||
:Acute promyelocytic leukaemia with t(15;17)(q22;q12); PML-RARA | |||
:AML with t(9;11)(p22;q23); MLLT3-MLL | |||
:AML with t(6;9)(p23;q34); DEK-NUP214v AML with inv(3)(q21q26.2) or t(3;3)(q21;q26.2);RPN1-EVI1 | |||
:AML (megakaryoblastic) with t(1;22)(p13;q13);RBM15-MKL1 | |||
:AML with mutated NPM1 | |||
:AML with mutated CEBPA | |||
:AML with myelodysplasia-related changes | |||
:Therapy-related myeloid neoplasms | |||
:Acute myeloid leukaemia, NOS | |||
:AML with minimal differentiation | |||
:AML without maturation | |||
:AML with maturation | |||
:Acute myelomonocytic leukaemia | |||
:Acute monoblastic and monocytic leukaemia | |||
:Acute erythroid leukaemia | |||
:Acute megakaryoblastic leukaemia | |||
:Acute basophilic leukaemia | |||
:Acute panmyelosis with myelofibrosis | |||
:Myeloid sarcoma | |||
:Myeloid proliferations related to Down syndrome | |||
:Transient abnormal myelopoiesis | |||
:Myeloid leukaemia associated with Down syndrome | |||
:Blastic plasmacytoid dendritic cell neoplasm | |||
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'''Acute leukaemias of ambiguous lineage''' | |||
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:Acute undifferentiated leukaemia | |||
:Mixed phenotype acute leukaemia with t(9;22)(q34;q11.2); BCR-ABL1 | |||
:Mixed phenotype acute leukaemia with t(v;11q23); MLL rearranged | |||
:Mixed phenotype acute leukaemia, B/myeloid, NOS 152 | |||
:Mixed phenotype acute leukaemia, T/myeloid, NOS 153 | |||
:Mixed phenotype acute leukaemia, NOS - rare types | |||
:Other ambiguous lineage leukaemias | |||
:Natural killer (NK)-cell lymphoblastic leukaemia/lymphoma | |||
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'''Precursor lymphoid neoplasms''' | |||
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:B lymphoblastic leukaemia/lymphoma, NOS | |||
:B lymphoblastic leukaemia/lymphoma with recurrent genetic abnormalities | |||
:B lymphoblastic leukaemia/lymphoma with t(9:22)(q34;q11.2); BCR-ABL1 | |||
:B lymphoblastic leukaemia/lymphoma with t(v;11q23); MLL rearranged | |||
:B lymphoblastic leukaemia/lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1) | |||
:B lymphoblastic leukaemia/lymphoma with hyperdiploidy | |||
:B lymphoblastic leukaemia/lymphoma with hypodiploidy (Hypodiploid ALL) | |||
:B lymphoblastic leukaemia/lymphoma with t(5;14)(q31;q32); IL3-IGH | |||
:B lymphoblastic leukaemia/lymphoma with t(1;19) (q23;p13.3); E2A-PBX1(TCF3-PBX1) | |||
:T lymphoblastic leukaemia/lymphoma | |||
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'''Mature B-cell neoplasms''' | |||
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:Chronic lymphocytic leukaemia /small lymphocytic lymphoma | |||
:B-cell prolymphocytic leukaemia | |||
:Splenic marginal zone lymphoma | |||
:Hairy cell leukaemia | |||
:Splenic B-cell lymphoma/leukaemia, unclassifiable | |||
:Splenic diffuse red pulp small B-cell lymphoma | |||
:Hairy cell leukaemia-variant | |||
:Lymphoplasmacytic lymphoma | |||
:Heavy chain diseases | |||
:Gamma heavy chain disease | |||
:Mu heavy chain disease | |||
:Alpha heavy chain disease | |||
:Plasma cell neoplasms | |||
:Monoclonal gammopathy of undetermined significance (MGUS) | |||
: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 | |||
:Follicular lymphoma | |||
:Primary cutaneous follicle centre lymphoma | |||
:Mantle cell lymphoma | |||
:Diffuse large B-cell lymphoma (DLBCL), NOS | |||
:T cell/histiocyte-rich large B-cell lymphoma | |||
:Primary DLBCL of the CNS | |||
:Primary cutaneous DLBCL, leg type | |||
:EBV positive DLBCL of the elderly | |||
:DLBCL associated with chronic inflammation | |||
:Lymphomatoid granulomatosis | |||
:Primary mediastinal (thymic) large B-cell lymphoma | |||
:Intravascular large B-cell lymphoma | |||
:ALK positive large B-cell lymphoma | |||
:Plasmablastic lymphoma | |||
:Large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease | |||
:Primary effusion lymphoma | |||
:Burkitt lymphoma | |||
:B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and Burkitt lymphoma | |||
:B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma | |||
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'''Mature T- and NK-cell neoplasms''' | |||
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:T-cell prolymphocytic leukaemia | |||
:T-cell large granular lymphocytic leukaemia | |||
:Chronic lymphoproliferative disorder of NK cells | |||
:Aggressive NK cell leukaemia | |||
:Epstein-Barr virus (EBV) positive T-cell lymphoproliferative diseases of childhood | |||
:Systemic EBV+ T-cell lymphoproliferative disease of childhood | |||
:Hydroa vacciniforme-like lymphoma | |||
:Adult T-cell leukaemia/lymphoma | |||
:Extranodal NK/T-cell lymphoma, nasal type | |||
:Enteropathy-associated T-cell lymphoma | |||
:Hepatosplenic T-cell lymphoma | |||
:Subcutaneous panniculitis-like T-cell lymphoma | |||
:Mycosis fungoides | |||
:Sézary syndrome | |||
:Primary cutaneous CD30 positive T-cell lymphoproliferative disorders | |||
:Primary cutaneous peripheral T-cell lymphomas, rare subtypes | |||
:Primary cutaneous gamma-delta T-cell lymphoma | |||
:Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma | |||
:Primary cutaneous CD4 positive small/medium T-cell lymphoma | |||
:Peripheral T-cell lymphoma, NOS | |||
:Angioimmunoblastic T-cell lymphoma | |||
:Anaplastic large cell lymphoma, ALK positive | |||
:Anaplastic large cell lymphoma, ALK negative | |||
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'''Hodgkin lymphoma''' | |||
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:Nodular lymphocyte predominant Hodgkin lymphoma | |||
:Classical Hodgkin lymphoma | |||
:Nodular sclerosis classical Hodgkin lymphoma | |||
:Mixed cellularity classical Hodgkin lymphoma | |||
:Lymphocyte-rich classical Hodgkin lymphoma | |||
:Lymphocyte-depleted classical Hodgkin lymphoma | |||
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'''Immunodeficiency-associated lymphoproliferative disorders''' | |||
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:Lymphoproliferative diseases associated with primary immune disorders | |||
:Lymphomas associated with HIV infection | |||
:Post-transplant lymphoproliferative disorders (PTLD) | |||
:Plasmacytic hyperplasia and infectious- mononucleosis-like PTLD | |||
:Polymorphic PTLD | |||
:Monomorphic PTLD | |||
:Classical Hodgkin lymphoma type PTLD | |||
:Other iatrogenic immunodeficiency-associated lymphoproliferative disorders | |||
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'''Histiocytic and dendritic cell neoplasms''' | |||
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:Histiocytic sarcoma | |||
:Tumours derived from Langerhans cells | |||
:Langerhans cell histiocytosis | |||
:Langerhans cell sarcoma | |||
:Interdigitating dendritic cell sarcoma | |||
:Follicular dendritic cell sarcoma | |||
:Other rare dendritic cell tumours | |||
:Disseminated juvenile xanthogranuloma | |||
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== Miscellaneous Cancer Types == | == Miscellaneous Cancer Types == | ||