Page 318 - Textbook of Pathology, 6th Edition
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             TABLE 12.5: Laboratory Diagnosis of Hypochromic Anaemias.
              Test             Iron Deficiency  Chronic Disorders   Thalassaemia    Sideroblastic Anaemia
           1. MCV, MCH, MCHC   Reduced          Low normal-to-reduced  Very low     Very low
                                                                                    (except MCV raised in aquired type)
           2. Serum iron       Reduced          Reduced             Normal          Raised
           3. TIBC             Raised           Low-to-normal       Normal          Normal
           4. Serum ferritin   Reduced          Raised              Normal          Raised
                                                                                    (complete saturation)
           5. Marrow-iron stores  Absent        Present             High            High
           6. Iron in normoblasts  Absent       Absent              Present         Ring sideroblasts
           7. Hb electrophoresis  Normal        Normal              Abnormal        Normal



           Treatment                                           tions, the anaemia is complicated by other causes such as
                                                               iron, B  and folate deficiency, hypersplenism, renal failure
                                                                     12
           The treatment of secondary sideroblastic anaemia is  with consequent reduced erythropoietic activity, endocrine
           primarily focussed on removal of the offending agent. No  abnormalities etc. However, in general, 2 factors appear to
           definite treatment is available for hereditary and idiopathic  play significant role in the pathogenesis of anaemia in chronic
     SECTION II
           types of sideroblastic anaemias. However, pyridoxine is
           administered routinely to all cases of sideroblastic anaemia  disorders. These are: defective red cell production and reduced
           (200 mg per day for 2-3 months). Blood transfusions and other  red cell lifespan.
           supportive therapy are indicated in all patients.   1. Defective red cell production. Though there is abun-
              Differential diagnosis of various types of hypochromic  dance of storage iron in these conditions but the amount of
           anaemias by laboratory tests is summarised in Table 12.5.  iron available to developing erythroid cells in the marrow is
                                                               subnormal. The mononuclear phagocyte system is
           ANAEMIA OF CHRONIC DISORDERS                        hyperplastic which traps all the available free iron due to
                                                               the activity of iron binding protein, lactoferrin. A defect in
           One of the commonly encountered anaemia is in patients of  the transfer of iron from macrophages to the developing
           a variety of chronic systemic diseases in which anaemia  erythroid cells in the marrow leads to reduced availability
           develops secondary to a disease process but there is no actual  of iron for haem synthesis despite adequate iron stores,
           invasion of the bone marrow. A list of such chronic systemic  elevating serum ferritin levels. The defect lies in suppression
           diseases is given in Table 12.6. In general, anaemia in chronic  of erythropoieitn by inflammatory cytokines at some stage
           disorders is usually normocytic normochromic but can have  in erythropoiesis, and hepcidin which is the key iron
           mild degree of microcytosis and hypochromia unrelated to  regulatory hormone. These inflammatory cytokines include
           iron deficiency. The severity of anaemia is usually directly  TNF and IFN-β released in bacterial infections and tumours,
           related to the primary disease process. The anaemia is  and IL-1 and IFN-γ released in patients of rheumatoid
           corrected only if the primary disease is alleviated.
                                                               arthritis and autoimmune vasculitis (Fig. 12.17).
           Pathogenesis                                        2. Reduced red cell lifespan.  Decreased survival of
                                                               circulating red cells in chronic renal disease is attributed to
           A number of factors may contribute to the development of  hyperplastic mononuclear phagocyte system.
     Haematology and Lymphoreticular Tissues
           anaemia in chronic systemic disorders, and in many condi-
                                                                 Laboratory Findings
            TABLE 12.6:  Anaemias Secondary to Chronic Systemic
               Disorders.                                        The characteristic features of anaemia in these patients
           1. ANAEMIA IN CHRONIC INFECTIONS/INFLAMMATION         uncomplicated by other deficiencies are as under:
           a. Infections e.g. tuberculosis, lung abscess, pneumonia, osteomyelitis,  i) Haemoglobin. Anaemia is generally mild to moderate.
              subacute bacterial endocarditis, pyelonephritis.   A haemoglobin value of less than 8 g/dl suggests the
           b. Non-infectious  inflammations  e.g. rheumatoid arthritis, SLE,  presence of additional contributory factors.
              vasculitis, dermatomyositis, scleroderma, sarcoidosis, Crohn’s
              disease.                                           ii) Blood picture. The type of anaemia in these cases is
           c. Disseminated malignancies e.g. Hodgkin’s disease, disseminated  generally normocytic normochromic but may have slight
              carcinomas and sarcomas.                           microcytosis and hypochromia.
           2. ANAEMIA OF RENAL DISEASE e.g.                      iii) Absolute values. Red cell indices indicate that in spite
              uraemia, renal failure                             of normocytic normochromic anaemia, MCHC is slightly
           3. ANAEMIA OF HYPOMETABOLIC STATE e.g.                low.
              endocrinopathies (myxoedema, Addison's disease, hyperthyroidism,
              hypopituitarism, Addison’s disease), protein malnutrition, scurvy and  iv) Reticulocyte count. The reticulocyte count is generally
              pregnancy, liver disease.                          low.
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