2. HEMATOLOGY
Study of blood and blood forming
tissues
Key components of hematologic
system are:
Blood
Blood forming tissues
Bone marrow
Spleen
Lymph system
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
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.
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%
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
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.