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Anemia
Dr. Irtaza Rehman
(Author of the book The Extraordinary Life)
Learning Objectives
• To highlight the important concepts of different
types of anemia
• To learn the clinical approach to diagnose
different types of anemia
Q. 29 years old presents with
lethargy and irritability for the
last 5 years. Labs revealed Hb of
9.6, MCV 70 and MCHC is low.
WBC & Platelets are normal. She
was prescribed iron supplements,
yet after 2 months has Hb 10.
Which lab investigation should be
ordered to find the underlying
cause of persistent anemia?
• Ans. Hb electrophoresis
What is decreased in Anemia??
RBC
Hb Hct
Dec O2
carrying
capacity
Dec
healthy
RBCs
Why anemia??
• 1. Decreased red cell production
A. Hematopoietic cell damage (Infections, Drugs)
B. Factors deficiency (Iron for heme)
(VB12/Folate for DNA)
2. Increased Red cell loss
A. External blood loss
B. RBC destruction
Etiologic
Classification
TACSI
• Thalassemia
• Anemia of
Chronic disease
• Sideroblastic
anemia
• Iron deficiency
anemia
MCV < 80 fl
Microcytic Anemia
Q. How will you differentiate between
IDA and Anemia of chronic disease?
• TIBC is decreased in AOCD
Q. How will you differentiate between B-
Thalassemia major and minor?
• Increased Hb-F in major
• Increased Hb-A2 in minor
Target cells
(Inc Cell.mem:cell volume)
• Hb-C disease
• Asplenia
• Liver disease
• Iron deficiency
anemia
• Thalassemia
Q. A 22 years old man has
congenital anemia that has
required multiple transfusions of
RBCs for many years. On physical
examination, she has no
significant findings. However LFT
show reduced serum albumin.
Which of the following would
most likely appear in a liver
biopsy specimen?
Ans. Hemosiderin
(in hepatocytes)
Q. 65 years old lady treated for
arthritis now presented with
weakness and bruises.
Examination reveal
pancytopenia, Retic count 0.1%,
hypocellular bone marrow with
normal cell morphology.
Diagnosis is
• Ans. Aplastic Anemia
Normal: 0.5 -2.5%
• All Megaloblastic anemia
are Macrocytic anemia
but all Macrocytic anemia
are not Megaloblastic
anemia.
MCV > 100 fl MCV > 100 fl
Abnormally large blood
cells precursors in bone
marrow
FAT RBC
Folate def-Fetus (pregnancy)
Alcohal
Thyroid (hypothyroidism)
Reticulocytosis
B12 deficiency
Chronic liver disease
Drugs causing Macrocytic anemia
• Hydroxyurea
• Methotrexate
• Phenytoin
• Zidovudine
• Sulfonamides (Septran)
HMP-ZShunt
GIT resection and anemia
Gastrectomy of a patient done after 4 years
patient came with anemia
Megaloblastic anemia
Terminal ileum resection causes
Vit B12 deficiency anemia
• I can cause loss of sense of vibration
• I can cause tingling sensation
• I can cause positive Babinski sign
• I am more common in veggies
• I am associated with anemia
What am i?
M
C
H
C
MCV
Q. A patient has end stage
renal disease and is on
dialysis for 6 months. She has
received multiple blood
transfusions. Her Hb 8. MCV
86 and low MCHC. What type
of anemia does she have?
• A. Hyperchromic microcytic
• B. Normocytic hypochromic
• C. Normocytic normochromic
• D. Hyperchromic macrocytic
• E. Macrocytic hypochromic
Ans. B
Q. A pregnant lady for
antenatal visit having Hb
7. She was prescribed iron
supplements. This should
be given.
• A. Before meal
• B. After meal
• C. Early morning
• D. with citrus fruits (juice)
• E. with milk
Ans. D
Q. The most common cause of anemia in
pregnancy (If Serum ferritin is normal) is?
Ans. Hemodilution
Q. A pregnant lady came in her first
trimester, her Hb was 12. Now her Hb in
last trimester is 10.
Ans. Normal Physiologic (Relative) anaemia
Blood loss Anemia
• Acute blood loss  Normocytic normochromic
• Chronic blood loss  Initially N-N later on
Microcytic hypochrochromic (Iron deficiency
anemia)
Q. A boy had Road
traffic accident and
suddenly loses 1.5
liters of blood.
What will be seen
on peripheral
smear?
• Ans. Normocytic normochromic anemia
Drugs causing G6PD
• Sulfonamides
• Primaquine
• Aspirin
• Isoniazid, Ibuprufen
• Nitrofurantoin
Dapsone
Hemolytic anemia
• Presents with “Unconjugated Hyperbilirubinemia”
• Decreased haptoglobin
• Intrinsic hemolysis
• Extrinsic hemolysis
Intrinsic Hemolytic Anemia
• Hereditary spherocytosis  Small round
RBC with less surface area & no central pallor
• G6PD  Self limiting, only males, Heinz bodies
• Sickle cell anemia  Chronic leg ulcers,
autosplenectomy (Howel-Jolly bodies), acute chest
syndrome
(Membrane stability test)
• Autoimmune  Warm antibody H.A  IgG
• Autoimmune  Cold agglutinin disease  IgM
Coombs test positive
• Microangiopathic H.A  Schistiocyte (helmet cells)
• Macroangiopathic H.A  Schistiocyte (helmet cells)
• Infections
Extrinsic Hemolytic Anemia
Q. A boy having Hb 5.6 deeply
jaundiced. Plt 260,000 and TLC
10,000. Retic count 10%, conjugated
bilirubin 0.9, hypersplenism having
non healing ulcers, abdominal pain
after tooth extraction. Diagnosis?
• A. Hemolytic crisis
• B. Thrombotic crisis
• C. Vasoclusive crisis
• D. Sequestration crisis
• E. Aplastic crisis
Ans. A
One tricky Question
Q. Dapsone given to a lady for
treatment of erythema nodosum
by dermatologist. Now she has
decreased Hb, MCV is 110 fl.
Diagnosis is??
A. Megaloblastic anemia
B. G6PD anemia Ans. A
Anti D antibody can cause
Hemolytic anemia OR Anti D
antibody can prevent
hemolytic anemia???
BOTH 
Erythroblastosis fetalis
• Counseling for Rh+ father and Rh- mother should
be  Hemolytic disease of newborn may occur
• Rh agglutinins  predominantly IgG
• Maternal anti D antibodies cross placental barrier 
hemolytic anemia
• To prevent Rh incompatibility in second child,
mother should be given  Anti D antibody injection
Erythroblastosis fetalis
Diagnose quickly
• MCV/MCHC
• Retic count
• Iron profile
• LDH/Haptoglobin/In
direct bilirubin
• Coomb’s test
• Peripheral blood
smear
Jazakumullahu Khair ♥
(May ALLAH swt reward you with goodness)

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Anemia.pptx

  • 1. Anemia Dr. Irtaza Rehman (Author of the book The Extraordinary Life)
  • 2.
  • 3. Learning Objectives • To highlight the important concepts of different types of anemia • To learn the clinical approach to diagnose different types of anemia
  • 4. Q. 29 years old presents with lethargy and irritability for the last 5 years. Labs revealed Hb of 9.6, MCV 70 and MCHC is low. WBC & Platelets are normal. She was prescribed iron supplements, yet after 2 months has Hb 10. Which lab investigation should be ordered to find the underlying cause of persistent anemia? • Ans. Hb electrophoresis
  • 5. What is decreased in Anemia?? RBC Hb Hct Dec O2 carrying capacity Dec healthy RBCs
  • 6. Why anemia?? • 1. Decreased red cell production A. Hematopoietic cell damage (Infections, Drugs) B. Factors deficiency (Iron for heme) (VB12/Folate for DNA) 2. Increased Red cell loss A. External blood loss B. RBC destruction Etiologic Classification
  • 7. TACSI • Thalassemia • Anemia of Chronic disease • Sideroblastic anemia • Iron deficiency anemia MCV < 80 fl Microcytic Anemia
  • 8. Q. How will you differentiate between IDA and Anemia of chronic disease? • TIBC is decreased in AOCD Q. How will you differentiate between B- Thalassemia major and minor? • Increased Hb-F in major • Increased Hb-A2 in minor
  • 9. Target cells (Inc Cell.mem:cell volume) • Hb-C disease • Asplenia • Liver disease • Iron deficiency anemia • Thalassemia
  • 10. Q. A 22 years old man has congenital anemia that has required multiple transfusions of RBCs for many years. On physical examination, she has no significant findings. However LFT show reduced serum albumin. Which of the following would most likely appear in a liver biopsy specimen? Ans. Hemosiderin (in hepatocytes)
  • 11. Q. 65 years old lady treated for arthritis now presented with weakness and bruises. Examination reveal pancytopenia, Retic count 0.1%, hypocellular bone marrow with normal cell morphology. Diagnosis is • Ans. Aplastic Anemia
  • 13. • All Megaloblastic anemia are Macrocytic anemia but all Macrocytic anemia are not Megaloblastic anemia.
  • 14. MCV > 100 fl MCV > 100 fl Abnormally large blood cells precursors in bone marrow
  • 15. FAT RBC Folate def-Fetus (pregnancy) Alcohal Thyroid (hypothyroidism) Reticulocytosis B12 deficiency Chronic liver disease
  • 16. Drugs causing Macrocytic anemia • Hydroxyurea • Methotrexate • Phenytoin • Zidovudine • Sulfonamides (Septran) HMP-ZShunt
  • 17. GIT resection and anemia Gastrectomy of a patient done after 4 years patient came with anemia Megaloblastic anemia Terminal ileum resection causes Vit B12 deficiency anemia
  • 18. • I can cause loss of sense of vibration • I can cause tingling sensation • I can cause positive Babinski sign • I am more common in veggies • I am associated with anemia What am i?
  • 20. Q. A patient has end stage renal disease and is on dialysis for 6 months. She has received multiple blood transfusions. Her Hb 8. MCV 86 and low MCHC. What type of anemia does she have? • A. Hyperchromic microcytic • B. Normocytic hypochromic • C. Normocytic normochromic • D. Hyperchromic macrocytic • E. Macrocytic hypochromic Ans. B
  • 21. Q. A pregnant lady for antenatal visit having Hb 7. She was prescribed iron supplements. This should be given. • A. Before meal • B. After meal • C. Early morning • D. with citrus fruits (juice) • E. with milk Ans. D
  • 22. Q. The most common cause of anemia in pregnancy (If Serum ferritin is normal) is? Ans. Hemodilution Q. A pregnant lady came in her first trimester, her Hb was 12. Now her Hb in last trimester is 10. Ans. Normal Physiologic (Relative) anaemia
  • 23. Blood loss Anemia • Acute blood loss  Normocytic normochromic • Chronic blood loss  Initially N-N later on Microcytic hypochrochromic (Iron deficiency anemia)
  • 24. Q. A boy had Road traffic accident and suddenly loses 1.5 liters of blood. What will be seen on peripheral smear? • Ans. Normocytic normochromic anemia
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  • 26. Drugs causing G6PD • Sulfonamides • Primaquine • Aspirin • Isoniazid, Ibuprufen • Nitrofurantoin Dapsone
  • 27. Hemolytic anemia • Presents with “Unconjugated Hyperbilirubinemia” • Decreased haptoglobin • Intrinsic hemolysis • Extrinsic hemolysis
  • 28. Intrinsic Hemolytic Anemia • Hereditary spherocytosis  Small round RBC with less surface area & no central pallor • G6PD  Self limiting, only males, Heinz bodies • Sickle cell anemia  Chronic leg ulcers, autosplenectomy (Howel-Jolly bodies), acute chest syndrome (Membrane stability test)
  • 29. • Autoimmune  Warm antibody H.A  IgG • Autoimmune  Cold agglutinin disease  IgM Coombs test positive • Microangiopathic H.A  Schistiocyte (helmet cells) • Macroangiopathic H.A  Schistiocyte (helmet cells) • Infections Extrinsic Hemolytic Anemia
  • 30. Q. A boy having Hb 5.6 deeply jaundiced. Plt 260,000 and TLC 10,000. Retic count 10%, conjugated bilirubin 0.9, hypersplenism having non healing ulcers, abdominal pain after tooth extraction. Diagnosis? • A. Hemolytic crisis • B. Thrombotic crisis • C. Vasoclusive crisis • D. Sequestration crisis • E. Aplastic crisis Ans. A
  • 31. One tricky Question Q. Dapsone given to a lady for treatment of erythema nodosum by dermatologist. Now she has decreased Hb, MCV is 110 fl. Diagnosis is?? A. Megaloblastic anemia B. G6PD anemia Ans. A
  • 32. Anti D antibody can cause Hemolytic anemia OR Anti D antibody can prevent hemolytic anemia??? BOTH 
  • 34. • Counseling for Rh+ father and Rh- mother should be  Hemolytic disease of newborn may occur • Rh agglutinins  predominantly IgG • Maternal anti D antibodies cross placental barrier  hemolytic anemia • To prevent Rh incompatibility in second child, mother should be given  Anti D antibody injection Erythroblastosis fetalis
  • 35. Diagnose quickly • MCV/MCHC • Retic count • Iron profile • LDH/Haptoglobin/In direct bilirubin • Coomb’s test • Peripheral blood smear
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  • 42. Jazakumullahu Khair ♥ (May ALLAH swt reward you with goodness)