Topic Highlight
Copyright ©2009 The WJG Press and Baishideng.
World J Gastroenterol. Oct 7, 2009; 15(37): 4627-4637
Published online Oct 7, 2009. doi: 10.3748/wjg.15.4627
Table 2 Morphological classification
Microcytic anemia (MCV < 82 fL)
IDA
Thalassemia
Non thalassemic conditions associated with microcytosis
ACD (e.g. rheumatoid arthritis, Hodgkin’s lymphoma, chronic infection, neoplasia)
Sideroblastic anemia (e.g. hereditary, lead poisoning)
Normocytic anemia (MCV = 82-98 fL)
Nutritional anemia (iron deficiency, cobalamin y/o folate)
Anemia of renal insufficiency
Hemolytic anemia
Red cell intrinsic causes: membranopathy, enzymopathy, hemoglobinopathy
Red cell extrinsic causes: immune-mediated, microangiopathic, associated with infection, chemical agent (spider venoms), metabolic
ACD
Primary bone marrow disorder
Causes that are intrinsic to hematopoietic stem cells: bone marrow aplasia (idiopathic, PNH, Fanconi syndrome), pure red cell aplasia (acquired, congenital, Diamond-Blackfan syndrome), myelodysplastic syndrome
Extrinsic causes: drugs, toxins, radiation, viruses, immune-mediated, bone marrow infiltration (metastatic and lymphoma)
Macrocytic anemia (MCV > 98 fL)
Drugs (hydroxyurea, zidovudine, methotrexate)
Nutritional (vitamin B12 and folate deficiency)
Drug-induced hemolytic anemia
Dyserythropoiesis, myelodysplastic syndrome, clonal hematologic disorder
Hereditary hematologic disorders
Mild macrocytosis (MCV = 100-110 fL)
Reticulocytes
Excess alcohol intake, liver disease, smoking
Hypothyroidism, Waldenström’s macroglobulinemia
Copper deficiency, bone marrow aplasia, erythroblastopenic anemia
Down syndrome
Chronic obstructive pulmonary disease