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Iron deficiency anemia

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coenzyme transferrin Ferritin hemosiderin myoglobin iron bloodstream Red blood cells 63% Storage pool 38% Muscle 3.5% Coenzyme 0.4% diet cells Blood stream 0.4% iron ... – PowerPoint PPT presentation

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Title: Iron deficiency anemia


1
Iron deficiency anemia
  • Jiang shayi

2
iron
transferrin
bloodstream
Ferritin hemosiderin
myoglobin
coenzyme
3
diet
Red blood cells 63
Muscle 3.5
Coenzyme 0.4
Blood stream 0.4
Storage pool 38
cells
4
iron protoporphyrin
hemoglobin
5
pathogenesis
Hypochromic anemia
protoporphyrin
ferritin
Abnormality of CBC
Free erythrocyte protoporphyi ?
Serum ferrtin ?
6
cause
  • Blood loss (polyp intestinal, meckel
    devirticulum, hookworm disease)
  • A lack of iron in diet
  • An inability to absorb iron
  • Less iron storage

7
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

8
Clinical manifestation
  • pica
  • persistent eating of non-food items for a
    period of at least one month. Including dirt,
    clay, soap, chalk, burnt matches

9
Clinical manifestation
  • koilonychia
  • Lost convexity
  • Flat or concave

10
Laboratory examination
  • Serum iron (SI)
  • Serum iron binding capacity
  • Serum ferritin (SF)
  • Biopsy of bone marrow
  • Complete blood count (CBC)

11
Complete blood count
  • Mean corpuscular volume (MCV)
  • Mean corpuscular hemoglobin(MCH)
  • Mean corpuscular hemoglobin concentration(MCHC)

12
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13
A normal peripheral blood smear indicates the
appropriate appearance of red blood cells, with a
normal zone of central pallor .
14
Iron deficiency anemia
15
the MCV of the red blood cells is decreased, the
zone of central pallor is increased
16
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17
Biopsy of bone marrowiron stain
Reduced iron stores
Normal iron stores
18
Diagnosis
  • Patient history
  • Clinical manifestation
  • Complete blood count and iron metabolism tests
  • Clinical trial of iron supplementation

19
Diagnosis
  • Determination of etiology
  • Primary disease, such gastrointestinal
    malformation

20
Differential diagnosis
  • Thalassemia
  • Pulmonary hemosiderosis
  • Sideroblastic anemia

21
Thalassemia
  • Family history
  • Unusuall facies
  • Splenomegaly, hepatomegaly
  • Target cell
  • HbF, HbA or HbH, Hb Barts elevate

22
thalassemia
23
Pulmonary hemosiderosis
  • moderate to severe hypochromic anemia
  • recurrent pulmonary hemorrhage of unknown cause
  • cough, coughing up blood (hemoptysis)
  • lung tissue changes.

24
Sideroblastic anemia
  • Hypochromic anemia
  • Iron test are normal or increased
  • Bone marrow ringed sideroblast

25
Sideroblastic anemia
26
Therapy
  • Diet
  • Eating iron fortified food
  • Breast and cows milk are low in iron
  • Iron is better absorbed from breast milk than
    cows milk
  • Formula milks (???)are fortified with iron

27
Therapy
  • Supplement therapy
  • Ferrous sulfate
  • Dextran-iron
  • elemental iron 3-6mg/kg/d
  • Therapy should be continued for 3 months

28
Therapy
  • Treating for primary disease

29
Summary
metabolism
mechanism
cause
tests
manifastation
diagnosis
therapy
30
??!
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