Hematologic disease
This article needs more primary sources. (July 2018) |
Hematologic disease | |
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Specialty | Hematology |
Hematologic diseases are disorders which primarily affect the
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)
- red blood cellsor hemoglobin)
- Iron-deficiency anemia
- Megaloblastic anemia
- Vitamin B12 deficiency
- Folate deficiency
- red blood cells)
- Genetic disorders of RBC membrane
- Genetic disorders of RBC metabolism
- 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
- Warm antibody autoimmune hemolytic anemia
- Alloimmunehemolytic 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)
- Hemolytic disease of the newborn (HDN)
- Drug induced immune mediated hemolytic anemia
- Penicillin (high dose)
- Methyldopa
- Autoimmune hemolytic anemia
- 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
- neutrophils)
- Agranulocytosis
- Glanzmann's thrombasthenia
- 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)
- red blood cells)
- white blood cells)
- 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
- Christmas disease)
- Hemophilia C
- Von Willebrand disease
- Disseminated intravascular coagulation
- Protein S deficiency
- Antiphospholipid syndrome
- Disorders of platelets
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
- 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
- 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
- Lymphomas
Miscellaneous
- Hemochromatosis
- Asplenia
- Hypersplenism
- Monoclonal gammopathy of undetermined significance
- Hemophagocytic lymphohistiocytosis
- Tempi syndrome