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DR.RATHER WASEEM YOUSUF
MVSC VETY CLINICAL MEDICINE
RBC & WBC ABNORMALITIES
AND THEIR INTERPRETATION
HEMATOLOGY
 Study of blood and blood forming
tissues
 Key components of hematologic
system are:
Blood
Blood forming tissues
Bone marrow
Spleen
Lymph system
WHAT DOES BLOOD DOES
 Transportation
 Oxygen
 Nutrients
 Hormones
 Waste Products
 Regulation
 Fluid, electrolyte
 Acid-Base balance
 Protection
 Coagulation
 Fight Infections
Components of Blood
 Plasma
55%
 Blood Cells
45%
Three types
Erythrocytes/RBC
s
Leukocytes/WBCs
Thrombocytes/Pla
telets
Erythrocytes/Red Blood Cells
 Composed of hemoglobin
 Erythropoiesis
= RBC production
Stimulated by hypoxia
Controlled by erythropoietin
 Hormone synthesized in kidney
 Hemolysis
= destruction of RBCs
Releases bilirubin into blood stream
Leukocytes/White Blood Cells
5 types
Basophils
Eosinophils
Neutrophils
Monocytes
Lymphocytes
Types and Functions of Leukocytes
 Granulocytes
 Neutrophil
 Eosinophil
 Basophil
 Agranulocytes
 Lymphocyte
 Monocyte
 Phagocytosis, early phase
of inflammation
 Phagocytosis, parasitic
infections
 Inflammatory response,
allergic response
 Cellular, humoral immune
response
 Phagocytosis; cellular
immune response
TYPE CELL FUNCTION
Abnormalities of RBCs
Abnormal erythrocyte
morphology is found in
pathological states that
may be :
- abnormalities in size
(anisocytosis).
- In shape (poikilocytosis).
- In hemoglobin content.
- presence of inclusion
bodies
1-Variation in erythrocyte size
(anisocytosis)
1-Microcytosis:
Morphology:
- Decrease in the red cell size. Red cells are smaller
than normal.
Found in:- Iron deficiency anemia..
- Lead poisoning.
- Anemia of chronic disease.
1-Variation in erythrocyte size
(anisocytosis)
1-Microcytosis:
Morphology:
- Decrease in the red cell
size. Red cells are
smaller than normal.
Found in:- Iron
deficiency anemia..
- Lead poisoning.
- Anemia of chronic
disease
1-Variation in erythrocyte size
(anisocytosis)
2-Macrocytosis:
Morphology:
Increase in the size of a
red cell. Red cells are
larger than normal. May
be round or oval in shape,
the diagnostic
significance being
different.
Found in:
- Foloate and B12
deficiencies (oval)
- Ethanol (round)
- Liver disease (round)
- Reticulocytosis (round)
II-Variation in hemoglobin content
1-Hypochromasia:
Morphology:
Increase in the red cells'
central pallor which
occupies more than the
normal third of the red
cell diameter.
Found in:
- Iron deficiency
- Thalassaemia
any of the conditions
leading to Microcytosis
II-Variation in hemoglobin content
2- Polychromasia:
Morphology:
Red cells stain shades of blue-gray
as a consequence of uptake of
both eosin (by hemoglobin) and
basic dyes (by residual ribosomal
RNA). Often slightly larger than
normal red cells and round in
shape - round macrocytosis.
Found in:
Any situation with
reticulocytosis - for example
bleeding, hemolysis or
response to haemostatic
factor replacement.
Anemia Classifications
 Microcytic, hypochromic
 Microcytic, normochromic
 Normocytic, normochromic
 Macrocytic, normochromic
NORMOCYTIC, NORMOCHROMIC
ANEMIA
 MCV normal
 MCHC normal
 Examples:
acute blood loss
aplastic anemia
most leukemia's
bone marrow infiltration
MICROCYTIC, HYPOCHROMIC ANEMIA
 MCV decreased
 MCHC decreased
 Examples:
iron deficiency
thalassemia
lead poisoning
anemia of chronic disease
MICROCYTIC, NORMOCHROMIC ANEMIA
MCV decreased
MCHC normal
Examples:
mid-stage iron deficiency
thalassemia
MACROCYTIC, NORMOCHROMIC
ANEMIA
 MCV increased
 MCHC normal
 Examples:
folate deficiency
vitamin B12 deficiency
pernicious anemia
III- Variation of red cells shape
(Poikilocytosis)
RBCs may have different
shapes:
1- Spherocytosis:
Morphology:
Red cells are more spherical.
Lack the central area of pallor
on a stained blood film.
Found in:
- Hereditary spherocytosis
- Immune haemolytic anemia
- Zieve's syndrome
- Microangiopathic haemolytic
anemia
III- Variation of red cells shape
(Poikilocytosis)
2-Target Cells:
Morphology:
Red cells have an area of
increased staining which
appears in the area of
central pallor.
Found in:
-Obstructive liver disease
-Severe iron deficiency
- Thalassaemia
- Haemoglobinopathies
- Post splenectomy
III- Variation of red cells shape
(Poikilocytosis)
3- Ovalocytes:
Morphology:
oval shape red blood
cell
Found in:
- Thalassaemia major.
- Hereditary ovalocytosis.
- Sickle cell anemia
III- Variation of red cells shape
(Poikilocytosis)
4- Elliptocytosis:
Morphology:
The red cells are oval or
elliptical in shape. Long
axis is twice the short axis.
Found in:
- Hereditary elliptocytosis
- Megaloblastic anemia
- Iron deficiency
- Thalassaemia
- Myelofibrosis
III- Variation of red cells shape
(Poikilocytosis)
5- Tear Drop Cells:
Morphology:
Red cells shaped like a
tear drop or pear
Found in:
- Bone marrow fibrosis
- Megaloblastic anemia
- Iron deficiency
- Thalassaemia
III- Variation of red cells shape
(Poikilocytosis)
6- Blister cell:
Morphology:
Have accentric hallow
area.
Found in:
Microangiopathic
hemolytic anemia
III- Variation of red cells shape
(Poikilocytosis)
7- Schistocytosis:
Morphology:
Fragmentation of
the red cells.
Found in:
- DIC
- Micro angiopathic
haemolytic anemia
- Mechanical haemolytic
anemia
III- Variation of red cells shape
(Poikilocytosis)
8- Stomatocytosis:
Morphology:
Red cells with a central
linear slit or stoma. Seen
as mouth-shaped form in
peripheral smear.
Found in:
- Alcohol excess
- Alcoholic liver disease
- Hereditary
stomatocytosis
- Hereditary spherocytosis
III- Variation of red cells shape
(Poikilocytosis)
9- Burr (crenation )
cell:
Morphology:
Red cell with uniformly spaced,
pointed projections on their
surface.
Found in:
- hemolytic anemia
- Uremia.
- Megaloblastic anemia
III- Variation of red cells shape
(Poikilocytosis)
10- Keratocytes
(horn cell):
Morphology:
Part of the cell fuses back
leaving two or three horn-
like projections. The
keratocyte is a fragile cell
and remains in circulation
for only a few hours.
Found in:
- Uraemia
- Severe burns
- EDTA artifact
- Liver disease
III- Variation of red cells shape
(Poikilocytosis)
11- Acanthocytosis:
Morphology:
are red blood cells with
irregularly spaced
projections, these
projections very in width
but usually contain a
rounded end
Found in:
- Liver disease
- Post splenectomy
- Anorexia nervosa and
starvation
III- Variation of red cells shape
(Poikilocytosis)
12- Sickle Cells:
Morphology:
Sickle shaped red
cells
Found in:
Hb-S disease
III- Variation of red cells shape
(Poikilocytosis)
13- Rouleaux Formation:
Morphology:
Stacks of RBC's
resembling a stack of
coins.
Found in:
-Hyperfibrinogenaemia
-Hyperglobulinaemia
III- Variation of red cells shape
(Poikilocytosis)
14- Red cell-
agglutination:
Morphology:
Irregular clumps of red
cells
Found in:
- Cold agglutinins
- Warm autoimmune
hemolysis
III- Variation of red cells shape
(Poikilocytosis)
15- Nucleated red blood
cells.
These red blood cells are
released from the bone
marrow early into the
blood stream, due to the
need for oxygen. Normal
red blood cells do not
contain a nucleus on a
peripheral smear.
IV -Erythrocyte inclusion bodies
1- Howell-Jolly Bodies:
Morphology:
Small round cytoplasmic
red cell inclusion with
same staining
characteristics as nuclei
Found in:
- Post splenectomy
- Megaloblastic anemia
IV -Erythrocyte inclusion bodies
2- Siderotic Granules
(Pappenheimer
Bodies)
RBCs which contain no
hemoglobin iron granules.
They appear as dense blue,
irregular granules which
are unevenly distributed in
Wright stained RBCs.
Pappenheimer bodies can
be increased in hemolytic
anemia, infections and
post-splenectomy.
IV -Erythrocyte inclusion bodies
3- Basophilic stippling:
Morphology:
Considerable numbers of
small basophilic inclusions
in red cells.
Found in:
- Thalassaemia
- Megaloblastic anemia
- Hemolytic anemia
- Liver disease
- Heavy metal poisoning.
IV -Erythrocyte inclusion bodies
4- Heinz Bodies:
Represent denatured
hemoglobin
(methemoglobin - Fe+++)
within a cell. With a
supravital stain like crystal
violet, Heinz bodies appear
as round blue precipitates.
Presence of Heinz bodies
indicates red cell injury and
is usually associated with
G6PD-deficiency.
IV -Erythrocyte inclusion bodies
5- Cabot Rings:
Reddish-blue threadlike rings
in RBCs of severe
anemia's. These are
remnants of the nuclear
membrane and appear as a
ring or figure 8 pattern.
Very rare finding in patients
with Megaloblastic anemia,
severe anemia's, lead
poisoning, and
dyserythropoiesis.
IV -Erythrocyte inclusion bodies
6- Parasites of Red
Cell:
are protozoan parasites
which occur in many
species of birds and are
the cause of avian
malaria. Transmitted by
mosquitoes, infection
with Plasmodium can be
a cause of hemolytic
anemia
Erythrocyte inclusion bodies
Depiction of red blood
cell morphologies that
may appear on a
peripheral smear,
showing:
(A)Basophilicstippling
(B) Howell-Jolly bodies
(C)Cabot'sringbodies
(D) Heinz's bodies.
Leukocytes (White Blood Cells)
 The leukocytes, or white blood cells,
constitute only 1% of the total blood
volume.
 They originate in the bone marrow and
circulate throughout the lymphoid
tissues of the body.
 There they function in the
inflammatory and immune processes.
 They include:
 the granulocytes
 Neutrophils – 55-65%
 Eosinophils – 1-4%
 Basophils – 0-1%
 the lymphocytes – 20-40%
 the monocytes – 3-8%
Differential Count
Neutrophil
50 – 75 %
Eosinophil
0 – 3 %
Basophil
0 – 1 %
Lymphocyte
20 – 40 %
Monocyte
2 – 6 %
Abnormalities of WBCs(quantative)
 Leucocytosis – substantial increase in the
WBC count.
- Physiologic increase (no trauma/injury)
- Pathologic increase (trauma/pathology)
 Leucopenia – substantial decrease in the
WBC count.
 N.V. = 5,000 – 10,000/cu mm
Neutrophilia Neutropenia
 Infections,
Inflammation,
Metabolic disorders
 Acute hemorrhage,
corticosteroids
 Stress, post-surgery,
burns, HDN
 Lithium drugs,
neoplasms
 Decreased production
- Inherited/acquired stem cell
disorder
- Benzene toxicity, cytotoxic
drugs
 Increased destruction
- Immune mechanism,
sequestration
 BM depression, IM, varicella,
Typhoid
 SLE, hepatitis or any viral
infections
NEUTROPHILLS
Eosinophilia Eosinopenia
 Allergic disorders
(asthma)
 Parasitic infections
(nematodes)
 Skin disease (eczema)
 Hodgkin’s disease
 Scarlet Fever
 Pernicious anemia
 Stress due to
trauma or shock
 Mental distress
 Cushing’s
syndrome
 ACTH
administration
EOSINOPHILLS
BASOPHILIA BASOPENIA
 Chronic
myelocytic
leukemia.
 Polycythemia.
 Hodgkin’s
disease.
 Hyperthyroidism.
 Pregnancy.
Basophil
Lymphocytosis Lymphopenia
 Viral infections
(German measles )
 Infectious
Mononucleosis
(kissing dis.)
 Mumps (parotitis),
pertussis
 Tuberculosis, syphilis,
thyrotoxicosis
 Congestive heart
failure, SLE
 Renal failure
 Advanced
Tuberculosis
 High levels of
adrenal
corticosteroids
LYMPHOCYTES
MONOCYTES
 SBE, Syphilis,
Tuberculosis
 Protozoan infections
 Mycotic or fungal
infections
 Malaria, Systemic lupus
erythematosus
 Rheumatoid arthritis
 Monocytosis  Monocytopenia
 Lymphocytic
leukemia
 Aplastic anemia
Abnormalities of WBCs(qualitative)
 Morphologic abnormalities involving
either the nucleus or cytoplasm
 Functional abnormalities
 Inherited or Acquired
Toxic Granulation
Morphology
Increased granulation. Granulation
more basophilic and larger than
normal.
Found in
 Severe bacterial infection.
 Non specific finding - seen in
tissue damage of various types.
 Normal pregnancy.
 Therapy with cytokines
Dohle Bodies
Morphology
Small pale blue cytoplasmic
inclusions, often in the periphery
of the cell.
Consist of ribosomes and
endoplasmic reticulum
Found in
 Infective and inflammatory
states.
 Severe burns
 Tuberculosis
 Post chemotherapy
 Pregnancy
 May-Heggling Anomaly
Russell bodies
Morphology
are eosinophilic, large,
homogenous immunoglobulin-
containing inclusions usually.
Found in
a plasma cell undergoing excessive
synthesis of immunoglobulin; the
Russell body is characteristic of the
distended endoplasmic reticulum
This is one cell variation found
in multiple myeloma.
Hypersegmentation or right shift of
neutrophil nuclei
Morphology
Average lobe count increased OR
increased % of neutrophils with
5 - 6 lobes OR > 3% neutrophils
with 5 lobes or more.
Found in
 Megaloblastic anaemia
 Iron deficiency
 Chronic infection
 Liver disease
 Uraemia
Hypogranulation
Morphology
Reduced granulation in
neutrophil cytoplasm.
Found in
 Myelodysplastic syndromes
Phagocytosed Parasites
Morphology
Malaria - Plasmodium
falcifarum
Found in
 Severe malaria infection
Macro Neutrophils
Morphology
Twice the size of a normal
neutrophil with tetraploid DNA
content.
Found in
 Occasionally in the blood of
healthy subjects.
 Inherited
 Administration of G-CSF
 Megaloblastic anaemia
 Chronic infection
Shift To The Left
Morphology
Presence of precursor of
granulocytes in the peripheral blood
Found in
 Normal in pregnancy or neonate.
 Infections.
 Bone marrow fibrosis.
 Bone marrow infiltration by
malignancies
Pseudo Pelger Huet Anomaly
Morphology
Bilobed neutrophils with more
condensed chromatin
Found in
 Inherited Myelodysplastic
syndromes.
 Idiopathic myelofibrosis.
 Chronic granulocytic leukemia.
 Therapy with colchicine,
ibuprofen.
 Infectious mononucleosis,
malaria, myxedema.
 CLL
Neutrophil aggregation
Morphology
Small clumps of neutrophils.
Happens in vitro if EDTA
anticoagulated blood is allowed
to stand. May lead to incorrect
WBC.
Found in
 In vitro finding.
 Infectious mononucleosis.
 Bacterial infections.
 Auto immune disease.
Atypical Lymphocytes
Morphology
Pleomorphic. Large with diameter
of 15 - 30 µm. Abundant, strongly
basophilic cytoplasm. Basophilia
may be confined to the cytoplasmic
margins.
Found in
 Viral infections - EBV, CMV,
Hep A, Measles.
 Bacterial infections - brucella,
tuberculosis.
 Protozoa – malaria.
 Immunization.
 SLE.
RBC & WBC abnormalities and their interpretation

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RBC & WBC abnormalities and their interpretation

  • 1. DR.RATHER WASEEM YOUSUF MVSC VETY CLINICAL MEDICINE RBC & WBC ABNORMALITIES AND THEIR INTERPRETATION
  • 2. HEMATOLOGY  Study of blood and blood forming tissues  Key components of hematologic system are: Blood Blood forming tissues Bone marrow Spleen Lymph system
  • 3. WHAT DOES BLOOD DOES  Transportation  Oxygen  Nutrients  Hormones  Waste Products  Regulation  Fluid, electrolyte  Acid-Base balance  Protection  Coagulation  Fight Infections
  • 4. Components of Blood  Plasma 55%  Blood Cells 45% Three types Erythrocytes/RBC s Leukocytes/WBCs Thrombocytes/Pla telets
  • 5. Erythrocytes/Red Blood Cells  Composed of hemoglobin  Erythropoiesis = RBC production Stimulated by hypoxia Controlled by erythropoietin  Hormone synthesized in kidney  Hemolysis = destruction of RBCs Releases bilirubin into blood stream
  • 6. Leukocytes/White Blood Cells 5 types Basophils Eosinophils Neutrophils Monocytes Lymphocytes
  • 7. Types and Functions of Leukocytes  Granulocytes  Neutrophil  Eosinophil  Basophil  Agranulocytes  Lymphocyte  Monocyte  Phagocytosis, early phase of inflammation  Phagocytosis, parasitic infections  Inflammatory response, allergic response  Cellular, humoral immune response  Phagocytosis; cellular immune response TYPE CELL FUNCTION
  • 8. Abnormalities of RBCs Abnormal erythrocyte morphology is found in pathological states that may be : - abnormalities in size (anisocytosis). - In shape (poikilocytosis). - In hemoglobin content. - presence of inclusion bodies
  • 9. 1-Variation in erythrocyte size (anisocytosis) 1-Microcytosis: Morphology: - Decrease in the red cell size. Red cells are smaller than normal. Found in:- Iron deficiency anemia.. - Lead poisoning. - Anemia of chronic disease.
  • 10. 1-Variation in erythrocyte size (anisocytosis) 1-Microcytosis: Morphology: - Decrease in the red cell size. Red cells are smaller than normal. Found in:- Iron deficiency anemia.. - Lead poisoning. - Anemia of chronic disease
  • 11. 1-Variation in erythrocyte size (anisocytosis) 2-Macrocytosis: Morphology: Increase in the size of a red cell. Red cells are larger than normal. May be round or oval in shape, the diagnostic significance being different. Found in: - Foloate and B12 deficiencies (oval) - Ethanol (round) - Liver disease (round) - Reticulocytosis (round)
  • 12. II-Variation in hemoglobin content 1-Hypochromasia: Morphology: Increase in the red cells' central pallor which occupies more than the normal third of the red cell diameter. Found in: - Iron deficiency - Thalassaemia any of the conditions leading to Microcytosis
  • 13. II-Variation in hemoglobin content 2- Polychromasia: Morphology: Red cells stain shades of blue-gray as a consequence of uptake of both eosin (by hemoglobin) and basic dyes (by residual ribosomal RNA). Often slightly larger than normal red cells and round in shape - round macrocytosis. Found in: Any situation with reticulocytosis - for example bleeding, hemolysis or response to haemostatic factor replacement.
  • 14. Anemia Classifications  Microcytic, hypochromic  Microcytic, normochromic  Normocytic, normochromic  Macrocytic, normochromic
  • 15. NORMOCYTIC, NORMOCHROMIC ANEMIA  MCV normal  MCHC normal  Examples: acute blood loss aplastic anemia most leukemia's bone marrow infiltration
  • 16. MICROCYTIC, HYPOCHROMIC ANEMIA  MCV decreased  MCHC decreased  Examples: iron deficiency thalassemia lead poisoning anemia of chronic disease
  • 17. MICROCYTIC, NORMOCHROMIC ANEMIA MCV decreased MCHC normal Examples: mid-stage iron deficiency thalassemia
  • 18. MACROCYTIC, NORMOCHROMIC ANEMIA  MCV increased  MCHC normal  Examples: folate deficiency vitamin B12 deficiency pernicious anemia
  • 19. III- Variation of red cells shape (Poikilocytosis) RBCs may have different shapes: 1- Spherocytosis: Morphology: Red cells are more spherical. Lack the central area of pallor on a stained blood film. Found in: - Hereditary spherocytosis - Immune haemolytic anemia - Zieve's syndrome - Microangiopathic haemolytic anemia
  • 20. III- Variation of red cells shape (Poikilocytosis) 2-Target Cells: Morphology: Red cells have an area of increased staining which appears in the area of central pallor. Found in: -Obstructive liver disease -Severe iron deficiency - Thalassaemia - Haemoglobinopathies - Post splenectomy
  • 21. III- Variation of red cells shape (Poikilocytosis) 3- Ovalocytes: Morphology: oval shape red blood cell Found in: - Thalassaemia major. - Hereditary ovalocytosis. - Sickle cell anemia
  • 22. III- Variation of red cells shape (Poikilocytosis) 4- Elliptocytosis: Morphology: The red cells are oval or elliptical in shape. Long axis is twice the short axis. Found in: - Hereditary elliptocytosis - Megaloblastic anemia - Iron deficiency - Thalassaemia - Myelofibrosis
  • 23. III- Variation of red cells shape (Poikilocytosis) 5- Tear Drop Cells: Morphology: Red cells shaped like a tear drop or pear Found in: - Bone marrow fibrosis - Megaloblastic anemia - Iron deficiency - Thalassaemia
  • 24. III- Variation of red cells shape (Poikilocytosis) 6- Blister cell: Morphology: Have accentric hallow area. Found in: Microangiopathic hemolytic anemia
  • 25. III- Variation of red cells shape (Poikilocytosis) 7- Schistocytosis: Morphology: Fragmentation of the red cells. Found in: - DIC - Micro angiopathic haemolytic anemia - Mechanical haemolytic anemia
  • 26. III- Variation of red cells shape (Poikilocytosis) 8- Stomatocytosis: Morphology: Red cells with a central linear slit or stoma. Seen as mouth-shaped form in peripheral smear. Found in: - Alcohol excess - Alcoholic liver disease - Hereditary stomatocytosis - Hereditary spherocytosis
  • 27. III- Variation of red cells shape (Poikilocytosis) 9- Burr (crenation ) cell: Morphology: Red cell with uniformly spaced, pointed projections on their surface. Found in: - hemolytic anemia - Uremia. - Megaloblastic anemia
  • 28. III- Variation of red cells shape (Poikilocytosis) 10- Keratocytes (horn cell): Morphology: Part of the cell fuses back leaving two or three horn- like projections. The keratocyte is a fragile cell and remains in circulation for only a few hours. Found in: - Uraemia - Severe burns - EDTA artifact - Liver disease
  • 29. III- Variation of red cells shape (Poikilocytosis) 11- Acanthocytosis: Morphology: are red blood cells with irregularly spaced projections, these projections very in width but usually contain a rounded end Found in: - Liver disease - Post splenectomy - Anorexia nervosa and starvation
  • 30. III- Variation of red cells shape (Poikilocytosis) 12- Sickle Cells: Morphology: Sickle shaped red cells Found in: Hb-S disease
  • 31. III- Variation of red cells shape (Poikilocytosis) 13- Rouleaux Formation: Morphology: Stacks of RBC's resembling a stack of coins. Found in: -Hyperfibrinogenaemia -Hyperglobulinaemia
  • 32. III- Variation of red cells shape (Poikilocytosis) 14- Red cell- agglutination: Morphology: Irregular clumps of red cells Found in: - Cold agglutinins - Warm autoimmune hemolysis
  • 33. III- Variation of red cells shape (Poikilocytosis) 15- Nucleated red blood cells. These red blood cells are released from the bone marrow early into the blood stream, due to the need for oxygen. Normal red blood cells do not contain a nucleus on a peripheral smear.
  • 34. IV -Erythrocyte inclusion bodies 1- Howell-Jolly Bodies: Morphology: Small round cytoplasmic red cell inclusion with same staining characteristics as nuclei Found in: - Post splenectomy - Megaloblastic anemia
  • 35. IV -Erythrocyte inclusion bodies 2- Siderotic Granules (Pappenheimer Bodies) RBCs which contain no hemoglobin iron granules. They appear as dense blue, irregular granules which are unevenly distributed in Wright stained RBCs. Pappenheimer bodies can be increased in hemolytic anemia, infections and post-splenectomy.
  • 36. IV -Erythrocyte inclusion bodies 3- Basophilic stippling: Morphology: Considerable numbers of small basophilic inclusions in red cells. Found in: - Thalassaemia - Megaloblastic anemia - Hemolytic anemia - Liver disease - Heavy metal poisoning.
  • 37. IV -Erythrocyte inclusion bodies 4- Heinz Bodies: Represent denatured hemoglobin (methemoglobin - Fe+++) within a cell. With a supravital stain like crystal violet, Heinz bodies appear as round blue precipitates. Presence of Heinz bodies indicates red cell injury and is usually associated with G6PD-deficiency.
  • 38. IV -Erythrocyte inclusion bodies 5- Cabot Rings: Reddish-blue threadlike rings in RBCs of severe anemia's. These are remnants of the nuclear membrane and appear as a ring or figure 8 pattern. Very rare finding in patients with Megaloblastic anemia, severe anemia's, lead poisoning, and dyserythropoiesis.
  • 39. IV -Erythrocyte inclusion bodies 6- Parasites of Red Cell: are protozoan parasites which occur in many species of birds and are the cause of avian malaria. Transmitted by mosquitoes, infection with Plasmodium can be a cause of hemolytic anemia
  • 40. Erythrocyte inclusion bodies Depiction of red blood cell morphologies that may appear on a peripheral smear, showing: (A)Basophilicstippling (B) Howell-Jolly bodies (C)Cabot'sringbodies (D) Heinz's bodies.
  • 41. Leukocytes (White Blood Cells)  The leukocytes, or white blood cells, constitute only 1% of the total blood volume.  They originate in the bone marrow and circulate throughout the lymphoid tissues of the body.  There they function in the inflammatory and immune processes.  They include:  the granulocytes  Neutrophils – 55-65%  Eosinophils – 1-4%  Basophils – 0-1%  the lymphocytes – 20-40%  the monocytes – 3-8%
  • 42. Differential Count Neutrophil 50 – 75 % Eosinophil 0 – 3 % Basophil 0 – 1 % Lymphocyte 20 – 40 % Monocyte 2 – 6 %
  • 43. Abnormalities of WBCs(quantative)  Leucocytosis – substantial increase in the WBC count. - Physiologic increase (no trauma/injury) - Pathologic increase (trauma/pathology)  Leucopenia – substantial decrease in the WBC count.  N.V. = 5,000 – 10,000/cu mm
  • 44. Neutrophilia Neutropenia  Infections, Inflammation, Metabolic disorders  Acute hemorrhage, corticosteroids  Stress, post-surgery, burns, HDN  Lithium drugs, neoplasms  Decreased production - Inherited/acquired stem cell disorder - Benzene toxicity, cytotoxic drugs  Increased destruction - Immune mechanism, sequestration  BM depression, IM, varicella, Typhoid  SLE, hepatitis or any viral infections NEUTROPHILLS
  • 45. Eosinophilia Eosinopenia  Allergic disorders (asthma)  Parasitic infections (nematodes)  Skin disease (eczema)  Hodgkin’s disease  Scarlet Fever  Pernicious anemia  Stress due to trauma or shock  Mental distress  Cushing’s syndrome  ACTH administration EOSINOPHILLS
  • 46. BASOPHILIA BASOPENIA  Chronic myelocytic leukemia.  Polycythemia.  Hodgkin’s disease.  Hyperthyroidism.  Pregnancy. Basophil
  • 47. Lymphocytosis Lymphopenia  Viral infections (German measles )  Infectious Mononucleosis (kissing dis.)  Mumps (parotitis), pertussis  Tuberculosis, syphilis, thyrotoxicosis  Congestive heart failure, SLE  Renal failure  Advanced Tuberculosis  High levels of adrenal corticosteroids LYMPHOCYTES
  • 48. MONOCYTES  SBE, Syphilis, Tuberculosis  Protozoan infections  Mycotic or fungal infections  Malaria, Systemic lupus erythematosus  Rheumatoid arthritis  Monocytosis  Monocytopenia  Lymphocytic leukemia  Aplastic anemia
  • 49. Abnormalities of WBCs(qualitative)  Morphologic abnormalities involving either the nucleus or cytoplasm  Functional abnormalities  Inherited or Acquired
  • 50. Toxic Granulation Morphology Increased granulation. Granulation more basophilic and larger than normal. Found in  Severe bacterial infection.  Non specific finding - seen in tissue damage of various types.  Normal pregnancy.  Therapy with cytokines
  • 51. Dohle Bodies Morphology Small pale blue cytoplasmic inclusions, often in the periphery of the cell. Consist of ribosomes and endoplasmic reticulum Found in  Infective and inflammatory states.  Severe burns  Tuberculosis  Post chemotherapy  Pregnancy  May-Heggling Anomaly
  • 52. Russell bodies Morphology are eosinophilic, large, homogenous immunoglobulin- containing inclusions usually. Found in a plasma cell undergoing excessive synthesis of immunoglobulin; the Russell body is characteristic of the distended endoplasmic reticulum This is one cell variation found in multiple myeloma.
  • 53. Hypersegmentation or right shift of neutrophil nuclei Morphology Average lobe count increased OR increased % of neutrophils with 5 - 6 lobes OR > 3% neutrophils with 5 lobes or more. Found in  Megaloblastic anaemia  Iron deficiency  Chronic infection  Liver disease  Uraemia
  • 54. Hypogranulation Morphology Reduced granulation in neutrophil cytoplasm. Found in  Myelodysplastic syndromes
  • 55. Phagocytosed Parasites Morphology Malaria - Plasmodium falcifarum Found in  Severe malaria infection
  • 56. Macro Neutrophils Morphology Twice the size of a normal neutrophil with tetraploid DNA content. Found in  Occasionally in the blood of healthy subjects.  Inherited  Administration of G-CSF  Megaloblastic anaemia  Chronic infection
  • 57. Shift To The Left Morphology Presence of precursor of granulocytes in the peripheral blood Found in  Normal in pregnancy or neonate.  Infections.  Bone marrow fibrosis.  Bone marrow infiltration by malignancies
  • 58. Pseudo Pelger Huet Anomaly Morphology Bilobed neutrophils with more condensed chromatin Found in  Inherited Myelodysplastic syndromes.  Idiopathic myelofibrosis.  Chronic granulocytic leukemia.  Therapy with colchicine, ibuprofen.  Infectious mononucleosis, malaria, myxedema.  CLL
  • 59. Neutrophil aggregation Morphology Small clumps of neutrophils. Happens in vitro if EDTA anticoagulated blood is allowed to stand. May lead to incorrect WBC. Found in  In vitro finding.  Infectious mononucleosis.  Bacterial infections.  Auto immune disease.
  • 60. Atypical Lymphocytes Morphology Pleomorphic. Large with diameter of 15 - 30 µm. Abundant, strongly basophilic cytoplasm. Basophilia may be confined to the cytoplasmic margins. Found in  Viral infections - EBV, CMV, Hep A, Measles.  Bacterial infections - brucella, tuberculosis.  Protozoa – malaria.  Immunization.  SLE.