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280.9 Iron deficiency anemia, unspecified; 281 Other deficiency anemias. 281.0 pernicious anemia; 281.2 Anemia, folate deficiency; 281.3 Other specified megaloblastic anemias, not elsewhere classified; 282 Hereditary hemolytic anemias. 282.0 Hereditary spherocytosis; 282.2 G6PD; 282.5 Sickle-cell trait; 282.6 Sickle-cell anemia; 283 Acquired ...
Neutropenia – a type of leukopenia, with a specific deficiency in neutrophils [2] Thrombocytopenia – a deficiency of platelets; Pancytopenia – when all three types of blood cells; red blood cells, white blood cells, and platelets, are all deficient. This is a life-threatening disorder that is a characteristic of aplastic anemia. [3]
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 ...
Bone marrow suppression is a serious side effect of chemotherapy and certain drugs affecting the immune system such as azathioprine. [2] The risk is especially high in cytotoxic chemotherapy for leukemia. In the case of non-small-cell lung cancer, myelosuppression predisposition was shown to be modulated by enhancer mutations. [3]
Thrombotic microangiopathy (TMA) is a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury. [1] It may be seen in association with thrombocytopenia, anemia, purpura and kidney failure.
Normal count is in the range of 150 × 10 9 to 450 × 10 9 platelets per liter of blood, [1] but investigation is typically only considered if the upper limit exceeds 750 × 10 9 /L. When the cause is unknown, the term thrombocythemia is used, as either primary thrombocythemia or essential thrombocythemia .
B2. No evidence of iron deficiency stainable iron in the bone marrow or normal red cell mean corpuscular volume; B3. No evidence of polycythemia vera. hematocrit < midpoint of normal range or normal red cell mass in presence of normal iron stores; B4. No evidence of chronic myeloid leukemia. But the Philadelphia chromosome may be present in up ...
Sometimes there are obvious clinical clues to suggest underlying B12 deficiency for a cause of pancytopenia. [6] In this selected cases even with severe anemia blood product transfusions can be avoided and vitamin B12 treatment itself suffice. [ 7 ]