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Iron deficienc y anemia. Jiang shayi. iron. transferrin. bloodstream. Ferritin hemosiderin. myoglobin. coenzyme. diet. Red blood cells 63%. Muscle 3.5%. Coenzyme 0.4%. Blood stream 0.4%. Storage pool 38%. cells. iron + protoporphyrin. hemoglobin. pathogenesis.
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Iron deficiency anemia Jiang shayi
iron transferrin bloodstream Ferritin hemosiderin myoglobin coenzyme
diet Red blood cells 63% Muscle 3.5% Coenzyme 0.4% Blood stream 0.4% Storage pool 38% cells
iron + protoporphyrin hemoglobin
pathogenesis Hypochromic anemia protoporphyrin ferritin Abnormality of CBC Free erythrocyte protoporphyi ↑ Serum ferrtin ↓
cause • Blood loss (polyp intestinal, meckel devirticulum, hookworm disease) • A lack of iron in diet • An inability to absorb iron • Less iron storage
Clinical l manifestation • Pale skin color • Fatigue, irritability, dizziness, weakness, • shortness of breath in severe patient • Poor appetite, especially in infants and children with iron deficiency anemia
Clinical manifestation • pica persistent eating of non-food items for a period of at least one month. Including dirt, clay, soap, chalk, burnt matches
Clinical manifestation • koilonychia Lost convexity Flat or concave
Laboratory examination • Serum iron (SI) • Serum iron binding capacity • Serum ferritin (SF) • Biopsy of bone marrow • Complete blood count (CBC)
Complete blood count • Mean corpuscular volume (MCV) • Mean corpuscular hemoglobin(MCH) • Mean corpuscular hemoglobin concentration(MCHC)
A normal peripheral blood smear indicates the appropriate appearance of red blood cells, with a normal zone of central pallor .
the MCV of the red blood cells is decreased, the zone of central pallor is increased
Biopsy of bone marrow——iron stain Normal iron stores Reduced iron stores
Diagnosis • Patient history • Clinical manifestation • Complete blood count and iron metabolism tests • Clinical trial of iron supplementation
Diagnosis • Determination of etiology Primary disease, such gastrointestinal malformation
Differential diagnosis • Thalassemia • Pulmonary hemosiderosis • Sideroblastic anemia
Thalassemia • Family history • Unusuall facies • Splenomegaly, hepatomegaly • Target cell • HbF, HbA or HbH, Hb Barts elevate
Pulmonary hemosiderosis • moderate to severe hypochromic anemia • recurrent pulmonary hemorrhage of unknown cause • cough, coughing up blood (hemoptysis) • lung tissue changes.
Sideroblastic anemia • Hypochromic anemia • Iron test are normal or increased • Bone marrow ringed sideroblast
Therapy • Diet • Eating iron fortified food • Breast and cow’s milk are low in iron • Iron is better absorbed from breast milk than cow’s milk • Formula milks (配方奶)are fortified with iron
Therapy • Supplement therapy • Ferrous sulfate • Dextran-iron • elemental iron 3-6mg/kg/d • Therapy should be continued for 3 months
Therapy • Treating for primary disease
Summary metabolism mechanism cause tests manifastation diagnosis therapy