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APLASTIC AND HYPOPLASTIC ANEMIAS

APLASTIC AND HYPOPLASTIC ANEMIAS. Waggas Elaas. APLASTIC ANEMIA. Aplastic anemia is a severe, life threatening syndrome in which production of erythrocytes, WBCs, and platlets has failed. Aplastic anemia may occur in all age groups and both genders.

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APLASTIC AND HYPOPLASTIC ANEMIAS

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  1. APLASTIC AND HYPOPLASTIC ANEMIAS WaggasElaas

  2. APLASTIC ANEMIA • Aplastic anemia is a severe, life threatening syndrome in which production of erythrocytes, WBCs, and platlets has failed. • Aplastic anemia may occur in all age groups and both genders. • The disease is characterized by peripheral pancytopenia and accompanied by a hypocellular bone marrow. • Pancytopenia : a reduction in blood count of all cell lines, WBCs, RBCs, platelets.

  3. Pathophysiology • The underlying defect in all cases appears to be a reduction in the number of haemopoietic pluripotential stem cells, and a fault in the remaining stem cells or an immune reaction against them, which makes them unable to divide and differentiate sufficiently to populate the bone marrow

  4. Causes of aplasticanaemia.

  5. Other Causes of pancytopenia • Acute leukaemia • Megaloblasticanaemia • Paroxysmal nocturnal haemoglobinuria (PNH) • Myelofibrosis • Splenomegaly • Myeloma or lymphoma

  6. Clinical features • At any age with a peak incidence around 30 years. • A slight male predominance. • symptoms and signs resulting from anaemia, neutropenia or thrombocytopenia. • Infections, particularly of the mouth and throat, are common and generalized infections are life-threatening. • Bruising, bleeding gums, epistaxesand menorrhagia are frequent, and the usual presenting features, often with symptoms of anaemia. • The lymph nodes, liver and spleen are not enlarged.

  7. Laboratory findings • Anaemia is normochromic, normocytic or macrocytic • The reticulocyte count is usually extremely low • Leucopenia. There is a selective fall in granulocytes, usually but not always to below 1.5 x 109/L. In severe cases, the lymphocyte count is also low. The neutrophils appear normal. • Thrombocytopenia is always present and, in severe cases, is less than 20 x 109/L. • There are no abnormal cells in the peripheral blood.

  8. The bone marrow is hypocellular, with loss of haemopoietic tissue and replacement by fat which comprises over 75% of the marrow. The main cells present are lymphocytes and plasma cells. Megakaryocytes in particular are severely reduced or absent.

  9. The disease must be distinguished from other causes of pancytopenia. • This is done by examination of the bone marrow samples for Cytogenetic analysis, flow-cytometry, and for morphology of cells and the marrow microenviromnent.

  10. HYPOCELLULAR BONE MARROW IN APLASTIC ANEMIA HYPOCELLULAR NORMOCELLULAR

  11. RELATED DISORDERS 1. Pure red cell aplasia Characterized by a selective decrease in erythroid precursor cells in the bone marrow. WBCs and platlets are unaffected. 2. Congenital dyserythropoieticanaemia. Hereditary refractory anaemias characterized by ineffective erythropoiesis and erythroblast multinuclearity. 3. Myelodysplastic syndromes primary, neoplastic stem cell disorders that tend to terminate in acute leukemia

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