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Hematologic disease

Disorders of the blood and related organs

Field	Value
name	Hematologic disease

| Hematologic diseases are disorders which primarily affect the blood and blood-forming organs. Hematologic diseases include rare genetic disorders, anemia, HIV, sickle cell disease and complications from chemotherapy or transfusions.

Myeloid

Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis)
- Sickle cell disease
- Thalassemia
- Methemoglobinemia
Anemias (lack of red blood cells or hemoglobin)
- Iron-deficiency anemia
- Megaloblastic anemia
  - Vitamin B12 deficiency
    - Pernicious anemia
  - Folate deficiency
- Hemolytic anemias (destruction of red blood cells)
  - Genetic disorders of RBC membrane
    - Hereditary spherocytosis
    - Hereditary elliptocytosis
    - Congenital dyserythropoietic anemia
  - Genetic disorders of RBC metabolism
    - Glucose-6-phosphate dehydrogenase deficiency (G6PD)
    - Pyruvate kinase deficiency
  - Immune mediated hemolytic anemia (direct Coombs test is positive)
    - Autoimmune hemolytic anemia
      - Warm antibody autoimmune hemolytic anemia
        
        Idiopathic
        
        Systemic lupus erythematosus (SLE)
        
        Evans syndrome (antiplatelet antibodies and hemolytic antibodies)
      - Cold autoimmune hemolytic anemia
        
        Cold agglutinin disease
        
        Paroxysmal cold hemoglobinuria (rare)
        
        Infectious mononucleosis
    - Alloimmune hemolytic anemia
      - Hemolytic disease of the newborn (HDN)
        
        Rh disease (Rh D)
        
        ABO hemolytic disease of the newborn
        
        Anti-Kell hemolytic disease of the newborn
        
        Rhesus c hemolytic disease of the newborn
        
        Rhesus E hemolytic disease of the newborn
        
        Other blood group incompatibility (RhC, Rhe, Kid, Duffy, MN, P and others)
    - Drug induced immune mediated hemolytic anemia
      - Penicillin (high dose)
      - Methyldopa
  - Hemoglobinopathies (where these is an unstable or crystalline hemoglobin)
  - Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
  - Direct physical damage to RBCs
    - Microangiopathic hemolytic anemia
    - Secondary to artificial heart valve(s)
- Aplastic anemia
  - Fanconi anemia
  - Diamond–Blackfan anemia (inherited pure red cell aplasia)
  - Acquired pure red cell aplasia
Decreased numbers of cells
- Myelodysplastic syndrome
- Myelofibrosis
- Neutropenia (decrease in the number of neutrophils)
- Agranulocytosis
- Glanzmann's thrombasthenia
- Thrombocytopenia (decrease in the number of platelets)
  - Idiopathic thrombocytopenic purpura (ITP)
  - Thrombotic thrombocytopenic purpura (TTP)
  - Heparin-induced thrombocytopenia (HIT)
Myeloproliferative disorders (Increased numbers of cells)
- Polycythemia vera (increase in the number of cells in general)
- Erythrocytosis (increase in the number of red blood cells)
- Leukocytosis (increase in the number of white blood cells)
- Thrombocytosis (increase in the number of platelets)
- Myeloproliferative disorder
- Transient myeloproliferative disease
Coagulopathies (disorders of bleeding and coagulation)
- Thrombocytosis
- Recurrent thrombosis
- Disseminated intravascular coagulation
- Disorders of clotting proteins
  - Hemophilia
    - Hemophilia A
    - Hemophilia B (also known as Christmas disease)
    - Hemophilia C
  - Von Willebrand disease
  - Disseminated intravascular coagulation
  - Protein S deficiency
  - Antiphospholipid syndrome
- Disorders of platelets
  - Thrombocytopenia
  - Glanzmann's thrombasthenia
  - Wiskott–Aldrich syndrome

Hematological malignancies

Hematological malignancies
- Lymphomas
  - Hodgkin's disease
  - Non-Hodgkin's lymphoma {includes the next five entries}
    - Burkitt's lymphoma
    - Anaplastic large cell lymphoma
    - Splenic marginal zone lymphoma
    - Hepatosplenic T-cell lymphoma
    - Angioimmunoblastic T-cell lymphoma (AILT)
- Myelomas
  - Multiple myeloma
  - Waldenström macroglobulinemia
  - Plasmacytoma
- Leukemias increased WBC
  - Acute lymphocytic leukemia (ALL)
  - Chronic lymphocytic leukemia (CLL){now included in theCLL/SCLL type NHL}
  - Acute myelogenous leukemia (AML)
  - Acute megakaryoblastic leukemia (AMKL), a sub-type of acute myelogenous leukemia
  - Chronic Idiopathic Myelofibrosis (MF)
  - Chronic myelogenous leukemia (CML)
  - T-cell prolymphocytic leukemia (T-PLL)
  - B-cell prolymphocytic leukemia (B-PLL)
  - Chronic neutrophilic leukemia (CNL)
  - Hairy cell leukemia (HCL)
  - T-cell large granular lymphocyte leukemia (T-LGL)
  - Aggressive NK-cell leukemia

Miscellaneous

Hemochromatosis
Asplenia
Hypersplenism
- Gaucher's disease
Monoclonal gammopathy of undetermined significance
Hemophagocytic lymphohistiocytosis
Tempi syndrome

Hematological changes secondary to non-hematological disorders

Anemia of chronic disease
Infectious mononucleosis
AIDS
Malaria
Leishmaniasis

References

Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

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