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8/18/2019 Blood - 6 (Anemia)
1/9
1/19/20
ANEMIA(without blood)
Prof Dr Waqas Hameed
FATE OF RBC
Fate of RBC
Globin
- recycled
Heme
- Pyrole ring opened
- Free iron bound toTRANSFERRIN
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Old RBC
MACROPHAGE
(spleen, bone marrow)
Heme + Globin Recycled
Fe++ + ProtoporphyrinRecycled
BILIVERDIN
(Green compound)
BILIRUBIN
Bilirubin+
Albumin
Bilirubin-AlbuminComplex
B
L
O
O
D
Albumin
HEPATOCYTE
Bilirubin + Ligandin
BL
O
O
D
Bilirubin-Albumin Complex
L
I
V
E
R
Biliribun + Uridine diphosphoglucoronic acid
Biliribun diglucoronide
Gucoronyl Transferase
B
I
L
E
Biliribun diglucoronide
UROBILINOGEN STERCOBILINOGEN STERCOBILIN
FECES
U
R
O
B
I
L
I
N
O
G
E
N
KIDNEY
Urobilinogen
Urobilin
Anemia
• Qualitative or Quantitative deff. of Hemoglobin
Deff. of Hemoglobin in blood
too little Hb
too few RBC’s
Most common blood disorder
Normal RBC – NORMOCYTIC NORMOCHROMIC
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Anemia - Classification
• Blood Loss Anemoa – Hemorrhagic
• Aplastic Anemia – Deficient production
• Megaloblastic Anemia
• Hemolytic Anemia
Blood Loss Anemia
• Hemorrhage
• Plasma replaced – 1 to 3 days
• Low conc. of RBC’s
Chronic Blood Loss
• Not enough iron absorbed
• Microcytic Hypochromic
Aplastic Anemia
• Bone Marrow Aplasia
• Exposure to GAMMA Ray Radiation – nuclear bomb
• Excessive x-ray treatment
• Industrial chemicals
• Drugs – chloramphenicol
Megaloblastic Anemia
• Vit B12 deff. & Folic Acid deff.
• Required for final maturation of RBC
• Essential for DNA synthesis
• MACROCYTES produced
• Carry O2 normally – fragile cell membranes
• Short life
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Pernicious Anemia
• Parietal cells – INTRINSIC FACTOR (glyocprotein)
Vit B12 in diet
Intrinsic Factor
– Parietal Cells
of Stomach
Vit B12
+
Intrinsic Factor
Absorbed from
Distal Ileum
Vit B12 protected from digestion
Megaloblastic Anemia
• Gastric Atrophy
• Chronic Atrophic Gastritis – autoimmune
• Blocking antibodies
• Gastric bypass surgery
• Tropical Sprue – Folic acid absorption ↓
Normocytic Anemia
• Hb – ↓
• RBC size (MCV) – normal
CAUSES
• Acute blood loss
• Aplastic anemia
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Blood Picture
• ↓ RBC
• ↓ Hb (smaller reduction)
• ↑ MCV
• ↑ MCH• MCHC - normal
IRON DEFF. ANEMIA
• MICROCYTIC HYPOCHROMIC
CAUSES
• Inadequate diet
• Inadequate absorption• Chronic blood loss
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Blood Picture
• ↓ RBC
• ↓ ↓ Hb
• ↓ MCV
• ↓ MCH
• ↓ MCHC
HEMOLYTIC ANEMIA
• Hereditary Spherocytosis
• Sickle Cell anemia
• Erythroblastosis Fetalis
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SICKLE CELL ANEMIA
• Hemoglobinopathy
• Valine replaces Glutamic acid residue at 6th
position in one of the two β-polypeptide chains
• Low O2 – RBC’s assume sickle shape
Anemia
(signs & symptoms)
• Weakness
• Fatigue
• General Malaise
• Dyspnea (shortness of breath on exertion)
• ↑ Cardiac output – palpitations
• Cardiac failure
PALLOR
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POLYCYTHEMIA
↑ Quantity of Red Blood cells
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Polycythemia
• Secondary Polycythemia
• Polycythemia Vera
Secondary Polycythemia
• High altitude – Hypoxia
• RBC count – 30% above normal (6-7 million/mm3)
PHYSIOLOGICAL POLYCYTHEMIA
• Natives of high altitude (14,000 – 17,000 feet)
Polycythemia Vera
• RBC count – (7-8 million/mm3)
• Hematocrit: 60-70%
• Genetic aberration
• Abnormal response to erythropoietin
• Viscosity of blood -increased
• Sluggish blood flow through
peripheral vessels
• Cyanotic tint (blueish) - skin
•