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ANEMIA
Dr. Mansour Aljabry
Head of Flow cytometry unit
Assistant professor & Consultant Hematologists
Hemoglobin??
α
β
β
α
Fe⁺⁺
Fe⁺⁺
Fe⁺⁺
Fe⁺⁺
Globin chain
Haem
Prophyrin ring
Iron atom
O2
O2
O2
O2
Hemoglobin structure
Dr. Aljabry
Hemoglobin
• Hemoglobin is the protein molecule in RBC that carries O2
from the lungs to the body's tissues and returns carbon CO2
from the tissues back to the lungs.
• Hemoglobin maintains the shape of RBC also.
Hematopoietic stem cell:
1- Self renewal
2- Cell differentiation
Hematopoiesis
Myeloid SC Erythroid Precursors
Transcriptional
Factor
Erythropoietin
GATA1
6
6
Late
Normoblast
Reticulocyte Erythrocyte
Basophilic
Normoblast
Erythroblast
Intermediate
Normoblast
+ ++ +++ ++ + -
Synthesis of
Hemoglobin
Erythropoiesis
The “Bone Marrow” is the major site with the need of:
Folic acid – Iron “Ferrous” – Vit B12 – Erythropoietin -Amino acids
minerals - other regulatory factors
Female
Male
Indices
11.5-15.5
13.5-17.5
Hemoglobin(g/dL)
36-48
40-52
Hematocrit (PCV) (%)
3.9-5.6
4.5-6.5
Red Cell Count (×10¹²)
80-95
Mean Cell Volume (MCV) (fL)
30-35
Mean Cell Hemoglobin (MCH)
(pg)
Hb
Macrocytic
Normocytic
Microcytic
MCV
Normochromic
Hypochromic
MCH
Normal Ranges
HCT
• An (without) -aemia (blood)
• Reduction of Hb concentration below the normal
range for the age and gender
• Leading to decreased O2 carrying capacity of
blood and thus O2 availability to tissues (hypoxia)
ANEMIA
Clinical Features
Presence or absence of clinical feature depends on:
1-Speed of onset :
Rapidly progressive anemia causes more symptoms than slow onset
anemia due to lack of compensatory mechanisms:
(cardiovascular system, BM &O2 dissociation curve
2-Severity:
• Mild anemia :no symptoms usually
• Symptoms appear if Hb less than 9g/dL
3- Age:
• Elderly tolerate anemia less than young patients
• Weakness
• Headache
• Pallor
• Lethargy
• Dizziness
• Palpitation (tachycardia)
• Angina
• Cardiac failure
Related to anemia
Related to compensatory
mechanism
Clinical Features
1-General features of anemia
Specific signs are associated with particular types of anemia :
 Spoon nail with iron deficiency,
 Leg ulcers with sickle cell anemia
 Jaundice with hemolytic anemia
 bone deformities in thalassemia major
2-Specific features
Classification of
Anemia
Hypochromic
microcytic
anemia
Hemoglobin
Prophyrin
Iron
Globin chain
Thalassemia
Iron def.
anemia
Sidroblastic
anemia
DNA
DNA
synthesis
Megaloblastic
anemia:
-B12 def.
-Folate def.
MDS
Macrocytic
anemia
RBC count
Hemolysis
RBC production
Acute
bleeding
Autoimmune
Enzymopathy
Membranopathy
Mechanical
Sickle cell anemia
BM failure:
-Chemotherapy
-Aplastic anemia
-Malignancy
Anemia of chronic
disease
Blood loss
Normocytic
normochromic
anemia
• Iron is among the abundant minerals on earth (6%).
• Iron deficiency is the most common disorder( 24%).
• Limited absorption ability :
1-Only 5-10% of taken iron will be absorbed
2- Inorganic iron can not be absorbed easily.
• Excess loss due to hemorrhage
Iron Deficiency Anemia
!
08/08/1444
14
Daily absorption ≈1 mg
Circulating
hemoglobin
(2.5g)
Bone marrow
erythroblast
(150mg)
Daily loss ≈1 mg
Liver and muscle
myoglobin (650mg)
Urine
faeces
Skin
nail
hair
Transferrin (4mg)
menstrual loss
(hemorrhage)
Macrophage (1g)
Storage forms:
Ferritin
Haemosiderin
Hepcidin
BM macrophage
- ve
IL6
Tfr2
+ve
Hypoxia
Iron for
erythropoeisis
Factor reducing absorption
Factors favoring absorption
Inorganic iron
Haem iron
Ferric iron Fe+++
Ferrous Iron (Fe++)
Alkalines
Acid
Iron overload
Iron def
Tea
Pregnancy
Increased hepcidin
Hemochromatosis
Precipitating agent(phenol)
Solubilizing agent (Sugar)
Iron Absorption
1-Body Iron status:
Increased demands
(iron def.,pregnancy..)
Low iron stores high absorption
Iron overload Full iron stores Low absorption
2- Content and form of dietary iron
More Iron
Heam Iron
More
absorption
3- Balance between dietary enhancers&Inhibitory factors:
Meat (haem iron)
Fruit (Vitamin C)
Sugar (Solubilizing agent )
Acids
Dairy foods (calcium)
High fiber foods (phytate)
Coffee &tea (polyphenoles)
Anti -Acids
Enhancers Inhibitors
Iron Absorption
Ferrous Iron
1-Chronic blood loss:
• GIT Bleeding: peptic ulcer, esophageal varices , hookworm cancer
• Uterine bleeding
• Hematuria
2- Increased demands:
• Immaturity
• Growth
• Pregnancy
• EPO therapy
3-Malabsorption:
• Enteropathy
• Gastrectomy
4-Poor diet: Rare as the only cause (rule out other causes)
Causes of IDA
4
Iron def.
anemia
3
Latent
2
Pre-latent
1
Normal
Low
Low
Low
Normal
Stores
Low
Low
Normal
Normal
MCV/MCH
Low
Normal
Normal
Normal
Hemoglobin
Development of IDA
Signs of
anemia
20
Beside symptoms and signs of anaemia +/- bleeding patients present with:
(a): Koilonychia (spoon-shaped nails)
(b): Angular stomatitis and/or glossitis
(c): Dysphagia due to pharyngeal web (Plummer-Vinson syndrome)
Signs and symptoms of IDA
a
c
b
Investigation
Microcytic hypochromic anemia with:
• Anisocytosis( variation in size)
• Pokiliocytosis (variation in shape)
normal
Iron Studies
TIBC*
• Serum Iron
• Serum ferritin
• Transferrin
saturation
• Low serum iron
• Low serum ferritin
• Low transferrin
saturation
high TIBC
Normal IDA
TIBC : total iron binding capacity of transferrin
Iron Studies
Low TIBC*
• High Serum Iron
• High Serum ferritin
• High Transferrin
saturation
• Low serum iron
• Low serum ferritin
• Low transferrin
saturation
high TIBC
Thalassemia IDA
Normal
BM Iron stain (Perl’s stain): The gold standard but invasive procedure
Normal IDA: reduced or absent iron stores
(hemosiderin)
Investigation
Treatment of IDA
• Treat the underlying cause
• Iron replacement therapy:
Oral :( Ferrous Sulphate OD for 6 months)
Intravenous:( Ferric sucrose OD for 6 months)
Hb should rise 2g/dL every 3 weeks
PREVENTION OF IDA
• Dietary modification
Meat is better source than vegetables.
• Food fortification (with ferrous sulphate)
• GIT disturbances ,staining of teeth & metallic taste.
• Iron supplementation:
For high risk groups.
Anemia of chronic disease
•Normochromic normocytic (usually) anemia caused by
decreased release of iron from iron stores due to raised
serum Hepcidin .
•Associated with
- Chronic infection including HIV, malaria
- Chronic inflammations
-Tissue necrosis
-Malignancy
Hepcidin
BM macrophage
IL-6
IL-1
TNF
no Iron for
erythropoeisis
+ve
Tuberculosis
SLE
Carcinoma
Lymphoma
- ve
29
Management:
Treat the underlying cause
Iron replacement +/- EPO
• Normocytic normochromic or mildly microcytic anaemia
• Low serum iron and TIBC
• Normal or high serum ferritin ( acute phase reactant)
• High haemosiderin in macrophages but low in normoblasts
Work-up and treatment

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ENGLISH5 QUARTER4 MODULE1 WEEK1-3 How Visual and Multimedia Elements.pptx
 

Anemia.pptx

  • 1. ANEMIA Dr. Mansour Aljabry Head of Flow cytometry unit Assistant professor & Consultant Hematologists
  • 4. Hemoglobin • Hemoglobin is the protein molecule in RBC that carries O2 from the lungs to the body's tissues and returns carbon CO2 from the tissues back to the lungs. • Hemoglobin maintains the shape of RBC also.
  • 5. Hematopoietic stem cell: 1- Self renewal 2- Cell differentiation Hematopoiesis Myeloid SC Erythroid Precursors Transcriptional Factor Erythropoietin GATA1
  • 6. 6 6 Late Normoblast Reticulocyte Erythrocyte Basophilic Normoblast Erythroblast Intermediate Normoblast + ++ +++ ++ + - Synthesis of Hemoglobin Erythropoiesis The “Bone Marrow” is the major site with the need of: Folic acid – Iron “Ferrous” – Vit B12 – Erythropoietin -Amino acids minerals - other regulatory factors
  • 7. Female Male Indices 11.5-15.5 13.5-17.5 Hemoglobin(g/dL) 36-48 40-52 Hematocrit (PCV) (%) 3.9-5.6 4.5-6.5 Red Cell Count (×10¹²) 80-95 Mean Cell Volume (MCV) (fL) 30-35 Mean Cell Hemoglobin (MCH) (pg) Hb Macrocytic Normocytic Microcytic MCV Normochromic Hypochromic MCH Normal Ranges HCT
  • 8. • An (without) -aemia (blood) • Reduction of Hb concentration below the normal range for the age and gender • Leading to decreased O2 carrying capacity of blood and thus O2 availability to tissues (hypoxia) ANEMIA
  • 9. Clinical Features Presence or absence of clinical feature depends on: 1-Speed of onset : Rapidly progressive anemia causes more symptoms than slow onset anemia due to lack of compensatory mechanisms: (cardiovascular system, BM &O2 dissociation curve 2-Severity: • Mild anemia :no symptoms usually • Symptoms appear if Hb less than 9g/dL 3- Age: • Elderly tolerate anemia less than young patients
  • 10. • Weakness • Headache • Pallor • Lethargy • Dizziness • Palpitation (tachycardia) • Angina • Cardiac failure Related to anemia Related to compensatory mechanism Clinical Features 1-General features of anemia Specific signs are associated with particular types of anemia :  Spoon nail with iron deficiency,  Leg ulcers with sickle cell anemia  Jaundice with hemolytic anemia  bone deformities in thalassemia major 2-Specific features
  • 12. Hypochromic microcytic anemia Hemoglobin Prophyrin Iron Globin chain Thalassemia Iron def. anemia Sidroblastic anemia DNA DNA synthesis Megaloblastic anemia: -B12 def. -Folate def. MDS Macrocytic anemia RBC count Hemolysis RBC production Acute bleeding Autoimmune Enzymopathy Membranopathy Mechanical Sickle cell anemia BM failure: -Chemotherapy -Aplastic anemia -Malignancy Anemia of chronic disease Blood loss Normocytic normochromic anemia
  • 13. • Iron is among the abundant minerals on earth (6%). • Iron deficiency is the most common disorder( 24%). • Limited absorption ability : 1-Only 5-10% of taken iron will be absorbed 2- Inorganic iron can not be absorbed easily. • Excess loss due to hemorrhage Iron Deficiency Anemia !
  • 14. 08/08/1444 14 Daily absorption ≈1 mg Circulating hemoglobin (2.5g) Bone marrow erythroblast (150mg) Daily loss ≈1 mg Liver and muscle myoglobin (650mg) Urine faeces Skin nail hair Transferrin (4mg) menstrual loss (hemorrhage) Macrophage (1g) Storage forms: Ferritin Haemosiderin
  • 16. Factor reducing absorption Factors favoring absorption Inorganic iron Haem iron Ferric iron Fe+++ Ferrous Iron (Fe++) Alkalines Acid Iron overload Iron def Tea Pregnancy Increased hepcidin Hemochromatosis Precipitating agent(phenol) Solubilizing agent (Sugar) Iron Absorption
  • 17. 1-Body Iron status: Increased demands (iron def.,pregnancy..) Low iron stores high absorption Iron overload Full iron stores Low absorption 2- Content and form of dietary iron More Iron Heam Iron More absorption 3- Balance between dietary enhancers&Inhibitory factors: Meat (haem iron) Fruit (Vitamin C) Sugar (Solubilizing agent ) Acids Dairy foods (calcium) High fiber foods (phytate) Coffee &tea (polyphenoles) Anti -Acids Enhancers Inhibitors Iron Absorption Ferrous Iron
  • 18. 1-Chronic blood loss: • GIT Bleeding: peptic ulcer, esophageal varices , hookworm cancer • Uterine bleeding • Hematuria 2- Increased demands: • Immaturity • Growth • Pregnancy • EPO therapy 3-Malabsorption: • Enteropathy • Gastrectomy 4-Poor diet: Rare as the only cause (rule out other causes) Causes of IDA
  • 20. 20 Beside symptoms and signs of anaemia +/- bleeding patients present with: (a): Koilonychia (spoon-shaped nails) (b): Angular stomatitis and/or glossitis (c): Dysphagia due to pharyngeal web (Plummer-Vinson syndrome) Signs and symptoms of IDA a c b
  • 21. Investigation Microcytic hypochromic anemia with: • Anisocytosis( variation in size) • Pokiliocytosis (variation in shape) normal
  • 22. Iron Studies TIBC* • Serum Iron • Serum ferritin • Transferrin saturation • Low serum iron • Low serum ferritin • Low transferrin saturation high TIBC Normal IDA TIBC : total iron binding capacity of transferrin
  • 23. Iron Studies Low TIBC* • High Serum Iron • High Serum ferritin • High Transferrin saturation • Low serum iron • Low serum ferritin • Low transferrin saturation high TIBC Thalassemia IDA Normal
  • 24. BM Iron stain (Perl’s stain): The gold standard but invasive procedure Normal IDA: reduced or absent iron stores (hemosiderin) Investigation
  • 25. Treatment of IDA • Treat the underlying cause • Iron replacement therapy: Oral :( Ferrous Sulphate OD for 6 months) Intravenous:( Ferric sucrose OD for 6 months) Hb should rise 2g/dL every 3 weeks
  • 26. PREVENTION OF IDA • Dietary modification Meat is better source than vegetables. • Food fortification (with ferrous sulphate) • GIT disturbances ,staining of teeth & metallic taste. • Iron supplementation: For high risk groups.
  • 27. Anemia of chronic disease •Normochromic normocytic (usually) anemia caused by decreased release of iron from iron stores due to raised serum Hepcidin . •Associated with - Chronic infection including HIV, malaria - Chronic inflammations -Tissue necrosis -Malignancy
  • 28. Hepcidin BM macrophage IL-6 IL-1 TNF no Iron for erythropoeisis +ve Tuberculosis SLE Carcinoma Lymphoma - ve
  • 29. 29 Management: Treat the underlying cause Iron replacement +/- EPO • Normocytic normochromic or mildly microcytic anaemia • Low serum iron and TIBC • Normal or high serum ferritin ( acute phase reactant) • High haemosiderin in macrophages but low in normoblasts Work-up and treatment