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• Introduction
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  • Myeloproliferative neoplasms (MPN)
    • Chronic myeloid leukaemia (CML), BCR-ABL1-positive
      • Chronic myeloid leukaemia (CML), BCR-ABL1-positive: chronic phase
      • Chronic myeloid leukaemia (CML), BCR-ABL1 positive: accelerated phase
      • Chronic myeloid leukaemia (CML), BCR-ABL1-positive: blast phase
        • Chronic myeloid leukaemia (CML), BCR-ABL1-positive: blast phase, lymphoblastic crisis
        • Chronic myeloid leukaemia (CML), BCR-ABL1-positive: blast phase, myeloblastic crisis
    • Polycythaemia vera (PV)
    • Primary myelofibrosis (PMF)
      • Prefibrotic/early primary myelofibrosis
      • Overt primary myelofibrosis
    • Essential thrombocythaemia (ET)
  • Mastocytosis
    • Systemic mastocytosis
      • Systemic mastocytosis
      • Indolent systemic mastocytosis (ISM)
      • Aggressive systemic mastocytosis (ASM)
  • Myeloid/lymphoid neoplasms with eosinophilia and gene rearrangement
    • Myeloid neoplasm with eosinophilia and with PDGFRA rearrangement
    • Lymphoid neoplasm with eosinophilia and with FGFR1 rearrangement
  • Myelodysplastic/myeloproliferative neoplasms (MDS/MPN)
    • Chronic myelomonocytic leukaemia (CMML)
      • Chronic myelomonocytic leukaemia, type 0 (CMML-0)
      • Chronic myelomonocytic leukaemia, type 1 (CMML-1)
      • Chronic myelomonocytic leukaemia, type 2 (CMML-2)
    • Atypical chronic myeloid leukaemia (aCML), BCR-ABL1-negative
    • Myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T)
  • Myelodysplastic syndromes (MDS)
    • Myelodysplastic syndrome with ring sideroblasts (MDS-RS)
      • Myelodysplastic syndrome with ring sideroblasts and with single lineage dysplasia (MDS-RS-SLD)
      • Myelodysplastic syndrome with ring sideroblasts and with multilineage dysplasia (MDS-RS-MLD)
    • Myelodysplastic syndrome with excess blasts (MDS-EB)
      • Myelodysplastic syndrome with excess blasts (MDS-EB-1)
      • Myelodysplastic syndrome with excess blasts (MDS-EB-2)
    • Myelodysplastic syndrome with isolated del(5q)
    • Childhood myelodysplastic syndrome
      • Refractory cytopenia of childhood
  • Myeloid neoplasms with germline predisposition
    • Myeloid neoplasms with germline predisposition and pre-existing platelet disorders
      • Myeloid neoplasms with germline RUNX1 mutation
  • Acute myeloid leukaemia and related precursor neoplasms
    • Acute myeloid leukaemia with recurrent genetic abnormalities
      • Acute myeloid leukaemia with t(8;21)(q22;q22); RUNX-RUNX1T1
      • Acute myeloid leukaemia with inv(16)(p131q22) or t(16;16)(p13.1;q22); CBFB-MYH11
      • Acute promyelocytic leukaemia with PML-RARA
      • Acute promyelocytic leukaemia with NPM1-RARA
    • Acute myeloid leukaemia, not otherwise specified
      • Acute myeloid leukaemia without maturation
      • Acute monoblastic/monocytic leukaemia
      • Acute megakaryoblastic leukaemia
  • Blastic plasmacytoid dendritic cell neoplasm
  • Acute leukaemias of ambiguous lineage
  • Precursor lymphoid neoplasms
    • B-lymphoblastic leukaemia/lymphoma, not otherwise specified
    • B-lymphoblastic leukaemia/lymphoma with recurrent genetic abnormalities
      • B-lymphoblastic leukaemia/lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1
    • T-lymphoblastic leukaemia/lymphoma
      • T-lymphoblastic leukaemia/lymphoma
  • Mature B-cell neoplasms
    • Chronic lymphocytic leukaemia / small lymphocytic lymphoma
      • Chronic lymphocytic leukaemia – classic morphology
      • Chronic lymphocytic leukaemia – atypical pleomorphic variant (mixed cell type)
      • Chronic lymphocytic leukaemia – transformation to diffuse large B-cell lymphoma (DLBCL), Richter’s syndrome
    • B-cell prolymphocytic leukaemia
    • Splenic marginal zone lymphoma
    • Hairy cell leukaemia
    • Lymphoplasmacytic lymphoma
      • Lymphoplasmacytic lymphoma
      • Waldenström macroglobulinaemia
    • Plasma cell neoplasms
      • Plasma cell myeloma
      • Plasma cell myeloma variants
        • Plasma cell leukaemia
    • Nodal marginal zone lymphoma
      • Nodal marginal zone lymphoma
    • Follicular lymphoma
      • Follicular lymphoma
    • Mantle cell lymphoma
      • Mantle cell lymphoma
      • Classic morphology
      • Small cell (CLL-like) variant
      • Pleomorphic variant
      • Blastoid variant
      • Marginal zone-like variant
    • Diffuse large B-cell lymphoma (DLBCL), not otherwise specified
      • Diffuse large B-cell lymphoma (DLBCL), not otherwise specified
      • Common morphological variants
        • Centroblastic morphological variant
        • Immunoblastic morphological variant
        • Anaplastic morphological variant
    • Burkitt lymphoma
  • Mature T- and NK-cell neoplasms
    • T-cell prolymphocytic leukaemia
      • T-cell prolymphocytic leukaemia
      • Small cell variant
    • T-cell large granular lymphocytic leukaemia
    • Hepatosplenic T-cell lymphoma
    • Sézary syndrome
    • Peripheral T-cell lymphoma, not otherwise specified
    • Angioimmunoblastic T-cell lymphoma and other nodal lymphomas of T follicular helper (TFH) cell origin
      • Angioimmunoblastic T-cell lymphoma
    • Anaplastic large-cell lymphoma, ALK-positive
  • Hodgkin lymphomas
    • Classic Hodgkin lymphoma
      • Classic Hodgkin lymphoma
      • Mixed cellularity classic Hodgkin lymphoma
  • Immunodeficiency-associated lymphoproliferative disorders
  • Histiocytic and dendritic cell neoplasms
  • Non-malignant haematology
    • Disorders of red blood cells
      • Normocytic normochromic anaemia
        • Congenital dyserythropoietic anaemia
          • Congenital sideroblastic anaemia
        • Paroxysmal nocturnal haemoglobinuria
      • Haemoglobinopathies
        • Beta thalassaemia major
        • Anaemia associated with haemoglobin Köln
      • Microcytic hypochromic anaemia
        • Iron-deficiency anaemia
      • Macrocytic anaemias
        • Megaloblastic anaemia
          • Vitamin B12 deficiency
      • Congenital haemolytic anaemias
        • Sickle cell anaemia
        • Hereditary spherocytosis
        • Pyruvate kinase deficiency
      • Acquired haemolytic anaemias
        • Autoimmune haemolytic anaemia
        • Autoimmune haemolytic anaemia with cold antibodies
        • Rouleaux
      • Anaemias induced by microorganisms
        • Leishmaniasis
          • Visceral leishmaniasis
        • Malaria
          • Plasmodium falciparum
          • Plasmodium malariae
          • Plasmodium ovale
          • Plasmodium vivax
    • Disorders of platelets
      • Thrombocytopenia
        • Congenital thrombocytopenia
          • MYH 9 mutation
            • May–Hegglin anomaly
    • Disorders with neutropenia
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