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Any fool can know. 
The point is to understand ! 
-- Albert Einstein 
Without Pathology, Medicine is quackery…!
DS3102: Clinical Haematology 
Pathology of 
RBC disorders (anemia) 
Dr. Shashidhar Venkatesh Murthy 
A/Prof. & Head of Pathology 
Less  More
3 
Anemia Introduction: 
“Anemia is, decreased red cell mass affecting 
tissue oxygenation” 
 Low Hb* or Low HCT * 
 Types: 
• Failure of production – Deficiency anemia (iron) 
• Excess destruction – Hemolytic anemia. (immune) 
 What is ‘polycythemia’ ? ( RBC) 
 What is spurious / false anemia? ( Plasma) 
O2 in - CO2 out 
RBC 
Hb + Enz 
Membrane
Normal Blood Film: 
RBC 
Hb + Enz + 
Membrane 
RBC 
WBC 
WBC 
RBC 
WBC
Anemia diagnosis: 
120 
Haemoglobin – 150 - 140 ±25 g gm/L 
PCV/HCT - 0.47 ±0.07, 0.42 ±0.05 % lit/lit (%) 
Packed Cell Volume 45 
RBC count - 5.5 ±1, 4.8 ± 1 x1012/L 
MCH - Hb/RBC - 30 ± 3 pg/RBC pg picogram (wt) 
• Average Hb in RBC 
MCV - PCV/RBC 90 ±10 – fl fl femto litres (vol) 
5 
Mean Cell Hb 30 
Mean Cell Vol 90 
Plasma 
WBC & PLT 
PCV / HCT
When your thinking is brilliant, you will be 
brilliant, but if your thinking is not brilliant 
you will not be brilliant, no matter how 
brilliant you may think you are….! 
-- Christian D. Larson 
Fake it until you make it…! 
-- Mohd. Ali. Boxer.
Clinical Features of Anemia & their 
Pathogenesis.
Anemia: Clinical Presentation 
 Extreme fatigue (tiredness) 
Decreased oxygen supply to tissues. 
 Chest pain (only in severe anemia) 
Myocardial ischemia. 
8
Anemia: Clinical Presentation 
 Pale skin 
Less Hb / RBC 
 Dizziness or lightheadedness 
Decreased oxygen supply to Brain. 
9 
RBC: Bring in O2, Take out CO2
Anemia Clinical Presentation: 
 Shortness of breath, light headedness. 
Decreased O2, Increased Co2. 
 Fast heart rate (tachycardia) 
Tissue hypoxia – Hypothalamus – 
sympathetic stimulation. 
10
Epithelial damage: 
 Brittle nails 
Fast dividing cells (epith) 
also need iron / nutrition 
Cytochrome enzymes 
 Stomatitis, Glossitis, Esophagitis. 
11
The mind uncontrolled and unguided 
will drag us down; and 
the mind controlled and guided will 
save us, free us. 
-- Swami Vivekananda
13 
Classification of Anemia: Pathogenesis 
 Decreased Production: 
• Nutrient Deficiency. 
• Iron def., Megaloblastic (B12/Folate) 
• Stem cell Deficiency : 
• Anemia of chronic disorders (ACD). 
• Aplastic anemia – bone marrow defect. 
 Increased loss / destruction: 
• Blood loss anemia – Acute / Chronic - bleeding. 
• Hemolytic anemia – Congenital / Acquired. 
• Acquired – Immune Haemolytic anemia (AIHA) 
• Congenital – Sickle, thalassemia etc. 
Top 5 Anemias 
1. Iron Deficiency. 
2. Megaloblastic. 
3. An. of Chronic Dis. 
4. Aplastic. 
5. Haemolytic - AIHA
BLAST Early Intermediate Late  Retic.  RBC 
Proerythroblast 
(Pronormoblast) 
Polychromatophilic 
Basophilic 
Normoblast 
Normoblast 
Reticulocyte 
Orthochromatophilic 
Normoblast 
Erythrocyte 
Anemia Pathogenesis: 
DNA: Megaloblastic Anemia 
Hb: Iron 
B12, Folate 
Iron Deficiency anemia 
Hemolytic anemia 
Immune 
14 
Aplastic anemia
Laboratory Diagnosis: Normal 
15 
WBC Scattergram 
RBC Histogram 
Neutrophil 
RBC 
Neutrophil 
Lymphocyte
16 
Classification of Anemia: 
 Decreased Production: 
• Nutrient Deficiency. 
• Iron def., Megaloblastic (B12/Folate) 
• Stem cell Deficiency : 
• Anemia of chronic disorders (ACD) – Iron transfer defect. 
• Aplastic anemia – bone marrow defect. 
 Increased loss / destruction: 
• Blood loss anemia – Acute / Chronic - bleeding. 
• Hemolytic anemia – Congenital / Acquired. 
• Acquired / External RBC defect 
– Immune AIHA (Warm/Cold), Mechanical, Drugs & Parasites 
• Congenital / Internal RBC defect 
– E.g. Sickle cell anemia, Thalassemia. 
Top 5 Anemias 
1. Iron Deficiency. 
2. Megaloblastic. 
Most common anemias
17 
Haemopoiesis in deficiency anemias 
Microcytic hypochromic Macrocytic, pancytopenia 
Iron Deficiency Normal Megaloblastic
Iron Deficiency - Megaloblastic 
 Causes: 
• Bleeding, Nutrition, 
Increased needs. 
 Pathogenesis: 
•  Iron - Hb - MCV 
 Morphology: 
• Microcytic, 
Hypochromic 
• Pencil cells. 
 Clinical Features: 
• koilonychia, glossitis, 
stomatitis. 
18 
 Causes: 
• Nutrition, gastritis, 
intestinal disorders, 
Cancer therapy. 
 Pathogenesis: 
• Abn. DNA*  all cells. 
 Morphology: 
• Macrocytic, 
Normochromic 
• Pancytopenia* 
 Clinical Features: 
• Jaundice mild, glossitis, 
chelitis, stomatitis.
Whatever you think, that you will be. 
If you think yourselves weak, 
weak you will be. 
If you think yourselves strong, 
strong you will be! 
-- Swami Vivekananda
Microcytic Anemia (IDA) 
Normal 
20
Iron Deficiency Anemia: 
21 
L 
1.Microcytic, Hypochromic – excess cell division, low Hb. 
2.Anisopoikilocytosis. – varying supply, abnormal hemopoiesis. 
3.Pencil forms. - ? cause
22 
Macrocytic Anemia (Meg.): 
Normal 
H 
N
Megaloblastic Anemia: 
Megaloblastic Bone Marrow Normal 
Macrocyte 
Hypersegmented 
Neutrophils 
Megaloblast 
1. Oval Macrocytes, Pancytopenia – Less cell division. 
2. Anisopoikilocytosis – Ineffective hempoiesis, Hemolysis. 
3. Hypersegmented neutrophils. - Megaloblasts (in marrow). 
23
Anemia of Chronic Disease: 
 Causes: 
• Chronic Infections, 
inflammations, malignancy & 
anemia of renal disease*. 
 Pathogenesis: 
• Inflammatory mediators (IFN, 
TNF) block iron transfer from 
store to RBC 
• Also decrease erythropoietin 
prod. 
 Morphology: 
• Mild Microcytic, Hypochromic. 
 Clinical Features: 
• Mild anemia, resistant to iron… 
24 IDA ? IDA / ACD ACD
“No doubt knowledge is valuable, 
but above it is Character” 
Knowledge without character is dangerous!
Aplastic A: BM Failure: immune, drugs, cancer.. 
Stem cell damage 
• Drugs, Immune 
• Viral Infections. 
26 
Dysplasia Normal BM Aplasia 
Clinical Features: 
Anemia, Infections & Bleeding. 
1. RBC - Anemia, 
2.  WBC - Leukopenia 
3.  PLT - Thrombocytopenia 
Leukemia 
Normocytic Pancytopenia
Our destiny is in our hands, 
What we think and do in the present 
determines what shall happen to us in 
the future. 
-- Christian D. Larson
28 
Mechanism & Types of Anemia : 
 Decreased Production: 
• Nutrient Deficiency. 
• Iron, B12 / Folate 
• Hemopoietic cell defect: 
• Anemia of chronic disorders (ACD) – low erythropoietin. 
• Aplastic, Hypoplastic – Drugs, Disease, Destruction. 
• Dysplastic & Neoplastic proliferative anemias. 
 Increased loss / destruction: 
• Blood loss anemia – bleeding, parasites, 
• Hemolytic anemia – Congenital / Acquired. 
• Acquired / External RBC defect 
– Immune (Warm/Cold), Mechanical, Drugs & Parasites 
• Congenital / Internal RBC defect 
– Defective Membrane (HS), Hb (Sickle, Thal) or Enzyme (G6PD)
Hemolytic anemia (acquired): 
 Causes: 
• Antibody to RBC – commonest (cold / warm) 
• Idiopathic, Drugs, infections, malaria, trauma. 
 Pathogenesis: 
• Damage  Hemolysis  Jaundice. 
 Morphology: 
• Spherocytes (warm) / RBC clumps (cold). 
 Clinical Features: 
• anemia, Jaundice. Splenomegaly in chronic. 
• Diagnosis: Coomb’s test (detects Ab on RBC) 
29 
COLD 
IgG 
WARM 
IgM 
COLD 
WARM
Congenital Hemolytic An.: 
1. Membrane Disorders 
• Hereditary Spherocytosis (HS) 
2. Enzyme Deficiencies. 
• G6PD Def. 
3. Hemoglobin Disorders 
• Globin deficiency: Thalassemia 
• Globin abnormal: Sickle cell an. 
30 
RBC 
• Cell Mem. 
• Enzymes 
• Hemoglobin 
Hemolysis 
Jaundice 
Clinical Features 
Thalassemia
Reticulocyte: Immature RBC 
Reticulocyte 
RBC 
(Bluish, Large, high MCV) 
RNA network within RBC – 
stained by methylene blue. 
Reticulocytes (Immature RBC)  Increased RBC production 
Reticulocytosis  Hemolytic anemia/bleeding 5-7 days 
31 
Polychromatophil 
Spherocyte 
Nucleated RBC
Never say No, never say, ‘I cannot’, for 
you are infinite. Even time and space 
are as nothing compared with your 
nature. You can do anything and 
everything. 
-- Swami Vivekananda
Anemia 
Diagnosis:
MCV 
Anemia 
Clinical Diagnosis 
Microcytic Normocytic Macrocytic 
Measure Ferritin 
Low Normal/high 
Iron def 
Anemia 
Anemia of 
chronic disease/ 
Congenital Hb dis. 
Reticulocyte count 
Normal Low 
high low Anemia of chronic disease 
Renal failure 
Marrow failure 
Hemolytic anemia 
or blood loss 
Measure B12 + folate 
Megaloblastic 
anemia 
34
If you need help, contact me… 
1. Office location – MS 39-136 (Townsville) 
2. Office Tel: 4781 4566 
3. Email: venkatesh.shashidhar@jcu.edu.au 
Need personal guidance? 
Email me for an appointment.
The power of thought is not a 
compelling force. It is a building 
force, and it is only when used in 
the latter sense that desirable 
results can be produced. 
-- Christian D. Larson
The pessimist waits for better times, 
and expects to keep on waiting; the 
optimist goes to work with the best 
that is at hand now, and proceeds to 
create better times. 
-- Christian D. Larson

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Haematology for Dental Students - RBC Disorders

  • 1. Any fool can know. The point is to understand ! -- Albert Einstein Without Pathology, Medicine is quackery…!
  • 2. DS3102: Clinical Haematology Pathology of RBC disorders (anemia) Dr. Shashidhar Venkatesh Murthy A/Prof. & Head of Pathology Less  More
  • 3. 3 Anemia Introduction: “Anemia is, decreased red cell mass affecting tissue oxygenation”  Low Hb* or Low HCT *  Types: • Failure of production – Deficiency anemia (iron) • Excess destruction – Hemolytic anemia. (immune)  What is ‘polycythemia’ ? ( RBC)  What is spurious / false anemia? ( Plasma) O2 in - CO2 out RBC Hb + Enz Membrane
  • 4. Normal Blood Film: RBC Hb + Enz + Membrane RBC WBC WBC RBC WBC
  • 5. Anemia diagnosis: 120 Haemoglobin – 150 - 140 ±25 g gm/L PCV/HCT - 0.47 ±0.07, 0.42 ±0.05 % lit/lit (%) Packed Cell Volume 45 RBC count - 5.5 ±1, 4.8 ± 1 x1012/L MCH - Hb/RBC - 30 ± 3 pg/RBC pg picogram (wt) • Average Hb in RBC MCV - PCV/RBC 90 ±10 – fl fl femto litres (vol) 5 Mean Cell Hb 30 Mean Cell Vol 90 Plasma WBC & PLT PCV / HCT
  • 6. When your thinking is brilliant, you will be brilliant, but if your thinking is not brilliant you will not be brilliant, no matter how brilliant you may think you are….! -- Christian D. Larson Fake it until you make it…! -- Mohd. Ali. Boxer.
  • 7. Clinical Features of Anemia & their Pathogenesis.
  • 8. Anemia: Clinical Presentation  Extreme fatigue (tiredness) Decreased oxygen supply to tissues.  Chest pain (only in severe anemia) Myocardial ischemia. 8
  • 9. Anemia: Clinical Presentation  Pale skin Less Hb / RBC  Dizziness or lightheadedness Decreased oxygen supply to Brain. 9 RBC: Bring in O2, Take out CO2
  • 10. Anemia Clinical Presentation:  Shortness of breath, light headedness. Decreased O2, Increased Co2.  Fast heart rate (tachycardia) Tissue hypoxia – Hypothalamus – sympathetic stimulation. 10
  • 11. Epithelial damage:  Brittle nails Fast dividing cells (epith) also need iron / nutrition Cytochrome enzymes  Stomatitis, Glossitis, Esophagitis. 11
  • 12. The mind uncontrolled and unguided will drag us down; and the mind controlled and guided will save us, free us. -- Swami Vivekananda
  • 13. 13 Classification of Anemia: Pathogenesis  Decreased Production: • Nutrient Deficiency. • Iron def., Megaloblastic (B12/Folate) • Stem cell Deficiency : • Anemia of chronic disorders (ACD). • Aplastic anemia – bone marrow defect.  Increased loss / destruction: • Blood loss anemia – Acute / Chronic - bleeding. • Hemolytic anemia – Congenital / Acquired. • Acquired – Immune Haemolytic anemia (AIHA) • Congenital – Sickle, thalassemia etc. Top 5 Anemias 1. Iron Deficiency. 2. Megaloblastic. 3. An. of Chronic Dis. 4. Aplastic. 5. Haemolytic - AIHA
  • 14. BLAST Early Intermediate Late  Retic.  RBC Proerythroblast (Pronormoblast) Polychromatophilic Basophilic Normoblast Normoblast Reticulocyte Orthochromatophilic Normoblast Erythrocyte Anemia Pathogenesis: DNA: Megaloblastic Anemia Hb: Iron B12, Folate Iron Deficiency anemia Hemolytic anemia Immune 14 Aplastic anemia
  • 15. Laboratory Diagnosis: Normal 15 WBC Scattergram RBC Histogram Neutrophil RBC Neutrophil Lymphocyte
  • 16. 16 Classification of Anemia:  Decreased Production: • Nutrient Deficiency. • Iron def., Megaloblastic (B12/Folate) • Stem cell Deficiency : • Anemia of chronic disorders (ACD) – Iron transfer defect. • Aplastic anemia – bone marrow defect.  Increased loss / destruction: • Blood loss anemia – Acute / Chronic - bleeding. • Hemolytic anemia – Congenital / Acquired. • Acquired / External RBC defect – Immune AIHA (Warm/Cold), Mechanical, Drugs & Parasites • Congenital / Internal RBC defect – E.g. Sickle cell anemia, Thalassemia. Top 5 Anemias 1. Iron Deficiency. 2. Megaloblastic. Most common anemias
  • 17. 17 Haemopoiesis in deficiency anemias Microcytic hypochromic Macrocytic, pancytopenia Iron Deficiency Normal Megaloblastic
  • 18. Iron Deficiency - Megaloblastic  Causes: • Bleeding, Nutrition, Increased needs.  Pathogenesis: •  Iron - Hb - MCV  Morphology: • Microcytic, Hypochromic • Pencil cells.  Clinical Features: • koilonychia, glossitis, stomatitis. 18  Causes: • Nutrition, gastritis, intestinal disorders, Cancer therapy.  Pathogenesis: • Abn. DNA*  all cells.  Morphology: • Macrocytic, Normochromic • Pancytopenia*  Clinical Features: • Jaundice mild, glossitis, chelitis, stomatitis.
  • 19. Whatever you think, that you will be. If you think yourselves weak, weak you will be. If you think yourselves strong, strong you will be! -- Swami Vivekananda
  • 21. Iron Deficiency Anemia: 21 L 1.Microcytic, Hypochromic – excess cell division, low Hb. 2.Anisopoikilocytosis. – varying supply, abnormal hemopoiesis. 3.Pencil forms. - ? cause
  • 22. 22 Macrocytic Anemia (Meg.): Normal H N
  • 23. Megaloblastic Anemia: Megaloblastic Bone Marrow Normal Macrocyte Hypersegmented Neutrophils Megaloblast 1. Oval Macrocytes, Pancytopenia – Less cell division. 2. Anisopoikilocytosis – Ineffective hempoiesis, Hemolysis. 3. Hypersegmented neutrophils. - Megaloblasts (in marrow). 23
  • 24. Anemia of Chronic Disease:  Causes: • Chronic Infections, inflammations, malignancy & anemia of renal disease*.  Pathogenesis: • Inflammatory mediators (IFN, TNF) block iron transfer from store to RBC • Also decrease erythropoietin prod.  Morphology: • Mild Microcytic, Hypochromic.  Clinical Features: • Mild anemia, resistant to iron… 24 IDA ? IDA / ACD ACD
  • 25. “No doubt knowledge is valuable, but above it is Character” Knowledge without character is dangerous!
  • 26. Aplastic A: BM Failure: immune, drugs, cancer.. Stem cell damage • Drugs, Immune • Viral Infections. 26 Dysplasia Normal BM Aplasia Clinical Features: Anemia, Infections & Bleeding. 1. RBC - Anemia, 2.  WBC - Leukopenia 3.  PLT - Thrombocytopenia Leukemia Normocytic Pancytopenia
  • 27. Our destiny is in our hands, What we think and do in the present determines what shall happen to us in the future. -- Christian D. Larson
  • 28. 28 Mechanism & Types of Anemia :  Decreased Production: • Nutrient Deficiency. • Iron, B12 / Folate • Hemopoietic cell defect: • Anemia of chronic disorders (ACD) – low erythropoietin. • Aplastic, Hypoplastic – Drugs, Disease, Destruction. • Dysplastic & Neoplastic proliferative anemias.  Increased loss / destruction: • Blood loss anemia – bleeding, parasites, • Hemolytic anemia – Congenital / Acquired. • Acquired / External RBC defect – Immune (Warm/Cold), Mechanical, Drugs & Parasites • Congenital / Internal RBC defect – Defective Membrane (HS), Hb (Sickle, Thal) or Enzyme (G6PD)
  • 29. Hemolytic anemia (acquired):  Causes: • Antibody to RBC – commonest (cold / warm) • Idiopathic, Drugs, infections, malaria, trauma.  Pathogenesis: • Damage  Hemolysis  Jaundice.  Morphology: • Spherocytes (warm) / RBC clumps (cold).  Clinical Features: • anemia, Jaundice. Splenomegaly in chronic. • Diagnosis: Coomb’s test (detects Ab on RBC) 29 COLD IgG WARM IgM COLD WARM
  • 30. Congenital Hemolytic An.: 1. Membrane Disorders • Hereditary Spherocytosis (HS) 2. Enzyme Deficiencies. • G6PD Def. 3. Hemoglobin Disorders • Globin deficiency: Thalassemia • Globin abnormal: Sickle cell an. 30 RBC • Cell Mem. • Enzymes • Hemoglobin Hemolysis Jaundice Clinical Features Thalassemia
  • 31. Reticulocyte: Immature RBC Reticulocyte RBC (Bluish, Large, high MCV) RNA network within RBC – stained by methylene blue. Reticulocytes (Immature RBC)  Increased RBC production Reticulocytosis  Hemolytic anemia/bleeding 5-7 days 31 Polychromatophil Spherocyte Nucleated RBC
  • 32. Never say No, never say, ‘I cannot’, for you are infinite. Even time and space are as nothing compared with your nature. You can do anything and everything. -- Swami Vivekananda
  • 34. MCV Anemia Clinical Diagnosis Microcytic Normocytic Macrocytic Measure Ferritin Low Normal/high Iron def Anemia Anemia of chronic disease/ Congenital Hb dis. Reticulocyte count Normal Low high low Anemia of chronic disease Renal failure Marrow failure Hemolytic anemia or blood loss Measure B12 + folate Megaloblastic anemia 34
  • 35. If you need help, contact me… 1. Office location – MS 39-136 (Townsville) 2. Office Tel: 4781 4566 3. Email: venkatesh.shashidhar@jcu.edu.au Need personal guidance? Email me for an appointment.
  • 36. The power of thought is not a compelling force. It is a building force, and it is only when used in the latter sense that desirable results can be produced. -- Christian D. Larson
  • 37. The pessimist waits for better times, and expects to keep on waiting; the optimist goes to work with the best that is at hand now, and proceeds to create better times. -- Christian D. Larson