©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
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 |
- Citation: Moreno Chulilla JA, Romero Colás MS, Gutiérrez Martín M. Classification of anemia for gastroenterologists. World J Gastroenterol 2009; 15(37): 4627-4637
- URL: https://www.wjgnet.com/1007-9327/full/v15/i37/4627.htm
- DOI: https://dx.doi.org/10.3748/wjg.15.4627