erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

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Erythrocyte series 1. rubriblast 2. prorubricyte 3. basophilic rubricyte 4. polychromatophilic rubricyte. 5. metarubricyte 6. reticulocyte 7. RBC STEM CELL (HAEMOCYTOBLAST) 1.Granulocyte series 2. Thrombocyte series 3.Erythrocyte series PRO-ERYTHROBLAST (Large nucleus, nucleoli ) EARLY ERYTHROBLAST (No nucleoli ) BASOPHILIC ERYTHROBLAST (Smaller, condensed chromatin) POLYCHROMATOPHILIC ERYTHROBLAST (Hb synthesis begins,) NORMOBLASTEarlystill contains viable nucleus Latenucleus becomes non-viable (RETICULOCYTE) No nucleusblue reticulum visible (Polychromatophilic macrocyte) NORMOCYTE (Erythrocyte) Adult red cell. Anuclear in mammals. Biconcave disc Stages of RBC Maturation

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Page 1: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Erythrocyte series

1. rubriblast

2. prorubricyte

3. basophilic rubricyte

4. polychromatophilic rubricyte.

5. metarubricyte

6. reticulocyte

7. RBC

STEM CELL (HAEMOCYTOBLAST)

1.Granulocyte series

2. Thrombocyte series

3.Erythrocyte series

• PRO-ERYTHROBLAST (Large nucleus, nucleoli )

• EARLY ERYTHROBLAST (No nucleoli )

• BASOPHILIC ERYTHROBLAST (Smaller, condensed chromatin)

• POLYCHROMATOPHILIC ERYTHROBLAST

• (Hb synthesis begins,)

• NORMOBLASTEarly–still contains viable nucleus

• Late–nucleus becomes non-viable

• (RETICULOCYTE) No nucleus–blue reticulum visible

• (Polychromatophilic macrocyte)

• NORMOCYTE

• (Erythrocyte) Adult red cell. Anuclear in mammals.

• Biconcave disc

Stages of RBC Maturation

Page 3: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Acanthocytosis

Irregularly spiculated red cells with net gain in lipids and an asymmetry between the 2 lipid layers

Causes: Hemolytic and non-hemolytic

Q-What is the abnormality? What is the mechanism?

Spherocytosis

Mechanisms of Spherocytosis:-

Microspherocytosis: deficiency

of red cell surface

Immune hemolytic anemias

Hereditary spherocytosis

Heinz-body hemolytic anemia

Clostridial sepsis, Severe burns

Hypophosphatemia

Loss of membrane lipids leading to a reduction in surface area due to deficiencies of

red cell-hereditary spherocytosis

Removal of membrane material form antibody coated red cells by macrophages-

Immune hemolytic anemia

Removal of membrane associated Heinz bodies with the adjacent membrane lipids

by the spleen- Heinz body hemolytic anemia

Page 4: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Target red cells

Basophilic stippling

Mechanisms of basophilic stippling

Reticulocyte Count

Reticulocytes

Increased membrane surface

no hemolysis, cells are

flexible

Volume loss

Decreased Hb: iron

deficiency,

Hemolytic anemias

Iron deficiency

Thalassemias

Lead poisoning -Diffuse fine or coarse blue dots in the red cell representing

usually RNA residue

Many small bluish dots in portion of erythrocytes; from staining of clustered polyribosomes in young circulating red cells

Failure to digest/clear residual RNA due to

– Acquired and congenital hemolytic anemias

– Lead poisoning (lead inhibits pyrimidine 5’ nucleotidase which normally digests residual RNA)

• An accurate reticulocyte count is key to the

initial classification of anemia

• Represent new, young, just released red cells

• ribosomal RNA

• Blue or black punctate spots

• The residual RNA is metabolised over time

• Measure of red cell production

• Reticulocytopenia

– Early iron deficiency

– Primary bone marrow failure

– Secondary bone marrow

failure

• Reticulocytosis

– Acute blood loss

– Splenic sequestration

– Hemolysis

• Immune

• Non-immune

• Infection

• Membrane

Page 5: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Tear drop red cells

Rouleaux and Agglutination

Stomatocytosis

• Bone marrow infiltration

– Fibrosis

– Tumors

– Granulomas

• Slit-shaped central pallor • Hereditary forms due to red

cell overhydration

– Na and water gain

– Hemolysis +

Page 6: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Howell-Jolly bodies

Mechanisms of Howell Jolly bodies

What do you call these cells?

How was it stained?

Heinz bodies in red cells

• Usually one or at most a few purplish inclusions in the red cell visible on routine peripheral smear exam

• The bodies represent aggregates of denatured hemoglobin

• Associated with states of splenic hypofunction or splenectomy

• Heinz Bodies are large, blue-purple intracytoplasmic inclusions, mostly attached to the inner cell membrane.

• Heinz bodies consist of either precipitated normal or unstable hemoglobin. • Represent oxidative injury to the red cell • These inclusions are found in cases of hemolysis due to unstable hemoglobins, oxidant drugs (such as

primaquine), hemolytic anemia associated with severe liver disease and G-6PD deficiency and other enzymopathies.

Page 7: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات
Page 8: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات
Page 9: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Iron deficiency anemia

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Page 10: Erythrocyte series عملي دكتور عبد الامير ّجامعة الكوفة تشخيصات

Microcytic hypochromic red cells

• Iron deficiency

• Lead poisoning

• Anemia of chronic diseases