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Define , describe and classify anemia
based on rbc indices and
reticulocyte count
• The normal range of hemoglobin
• values for adult males is 13.5–17.5 g/dL (135–
175 g/L) and that for
• adult females is 12–15 g/dL (120–150 g/L).
The World Health
• Organization (WHO) defines anemia as a
hemoglobin level <13 g/dL
• (130 g/L) in men and <12 g/dL (120 g/L) in
women
• careful history
• physical examination.
• Nutritional history related to drugs or alcohol
intake
family history of anemia
• Infection , blood in stool, lymphadenopathy,
splenomegaly, or petechiae.
• Splenomegaly and lymphadenopathy suggest
an underlying lymphoproliferative disease,
whereas petechiae suggest platelet
dysfunction
• forceful heartbeat, strong peripheral pulses,
and a systolic “flow”murmur. The skin and
mucous membranes may be pale
• Microcytosis is reflected by a lower than normal
MCV(<80), whereas high values (>100) reflect
macrocytosis
• Peripheral smear variations in cell size
(anisocytosis) and shape(poikilocytosis)
• polychromasia—red cells that are slightly
• larger than normal and grayish blue in color on
the Wright-Giemsa nucleated red cells,
• Howell-Jolly bodies, target cells, sickle cells
Reticulocyte count
• ranges from 1% to2% and reflects the daily
replacement of 0.8–1.0%
• They are identified by staining with a
supravital dye that precipitates the
ribosomalRNA . These precipitates appear as
blue or black punctate spots
• Normal serum iron ranges from 9 to 27
μmol/L (50–150 μg/dL),
• the normal TIBC is 54–64 μmol/L (300–360
μg/dL); the normal
• transferrin saturation ranges from 25 to 50%.
Bone marrow examination
• hypoproliferative anemia,
• Normal renal function, and normal iron status
• the myeloid/erythroid [M/E] ratio
• Iron stores
DEFINITION AND CLASSIFICATION OF
ANEMIA
• Hypoproliferative Anemias
• Maturation Disorders
• Blood Loss/Hemolytic Anemia
Hypoproliferative Anemias
• 75% of all cases of anemia
• marrow damage, iron deficiency, or
inadequate EPOstimulation
• normocytic, normochromic red cells, although
microcytic,hypochromic cells may be observed
with mild iron deficiency or longstanding
chronic inflammatory disease
• Bone marrow aspirate or biopsy
Maturation disorders
• anemia with an inappropriately low
reticulocyte production index, macro- or
microcytosis on smear, and abnormal red cell
indices suggests a maturation disorder.
• nuclear maturation defects, associated with
macrocytosis, and cytoplasmic maturation
defects, associated with microcytosis and
hypochromia usually from defects in
hemoglobin synthesis.
• Nuclear maturation defects result from
vitamin B12 or folic acid deficiency, drug
damage, or myelodysplasia.
• Cytoplasmic maturation defects result from
severe iron deficiency or abnormalities in
globin or heme synthesis
• Myelodysplasia: iron-encrusted mitochondria
surround the nucleus of the erythroid cell,
forming a ring
Blood Loss/Hemolytic Anemia
• polychromatophilic macrocytes.
• Acute, subacute,chronic blood loss
• Hemolytic intravascular or extravascular hemolysis
• family history, the pattern of clinical
• presentation, and—whether the disease is congenital
or acquired—
• careful examination of the peripheral blood smear
• Hb electrophoresis, dct , ict
• Thank you

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Define__describe_and_classify_anemia.pptx

  • 1. Define , describe and classify anemia based on rbc indices and reticulocyte count
  • 2. • The normal range of hemoglobin • values for adult males is 13.5–17.5 g/dL (135– 175 g/L) and that for • adult females is 12–15 g/dL (120–150 g/L). The World Health • Organization (WHO) defines anemia as a hemoglobin level <13 g/dL • (130 g/L) in men and <12 g/dL (120 g/L) in women
  • 3. • careful history • physical examination. • Nutritional history related to drugs or alcohol intake family history of anemia
  • 4. • Infection , blood in stool, lymphadenopathy, splenomegaly, or petechiae. • Splenomegaly and lymphadenopathy suggest an underlying lymphoproliferative disease, whereas petechiae suggest platelet dysfunction • forceful heartbeat, strong peripheral pulses, and a systolic “flow”murmur. The skin and mucous membranes may be pale
  • 5. • Microcytosis is reflected by a lower than normal MCV(<80), whereas high values (>100) reflect macrocytosis • Peripheral smear variations in cell size (anisocytosis) and shape(poikilocytosis) • polychromasia—red cells that are slightly • larger than normal and grayish blue in color on the Wright-Giemsa nucleated red cells, • Howell-Jolly bodies, target cells, sickle cells
  • 6.
  • 7.
  • 8.
  • 9. Reticulocyte count • ranges from 1% to2% and reflects the daily replacement of 0.8–1.0% • They are identified by staining with a supravital dye that precipitates the ribosomalRNA . These precipitates appear as blue or black punctate spots
  • 10.
  • 11. • Normal serum iron ranges from 9 to 27 μmol/L (50–150 μg/dL), • the normal TIBC is 54–64 μmol/L (300–360 μg/dL); the normal • transferrin saturation ranges from 25 to 50%.
  • 12. Bone marrow examination • hypoproliferative anemia, • Normal renal function, and normal iron status • the myeloid/erythroid [M/E] ratio • Iron stores
  • 13.
  • 14. DEFINITION AND CLASSIFICATION OF ANEMIA • Hypoproliferative Anemias • Maturation Disorders • Blood Loss/Hemolytic Anemia
  • 15. Hypoproliferative Anemias • 75% of all cases of anemia • marrow damage, iron deficiency, or inadequate EPOstimulation • normocytic, normochromic red cells, although microcytic,hypochromic cells may be observed with mild iron deficiency or longstanding chronic inflammatory disease • Bone marrow aspirate or biopsy
  • 16. Maturation disorders • anemia with an inappropriately low reticulocyte production index, macro- or microcytosis on smear, and abnormal red cell indices suggests a maturation disorder. • nuclear maturation defects, associated with macrocytosis, and cytoplasmic maturation defects, associated with microcytosis and hypochromia usually from defects in hemoglobin synthesis.
  • 17. • Nuclear maturation defects result from vitamin B12 or folic acid deficiency, drug damage, or myelodysplasia. • Cytoplasmic maturation defects result from severe iron deficiency or abnormalities in globin or heme synthesis • Myelodysplasia: iron-encrusted mitochondria surround the nucleus of the erythroid cell, forming a ring
  • 18. Blood Loss/Hemolytic Anemia • polychromatophilic macrocytes. • Acute, subacute,chronic blood loss • Hemolytic intravascular or extravascular hemolysis • family history, the pattern of clinical • presentation, and—whether the disease is congenital or acquired— • careful examination of the peripheral blood smear • Hb electrophoresis, dct , ict