Hema 1 Part 2 1 Flashcards

1
Q

PURPOSES OF BLOOD FILM EXAMINATION

A

• To differentiate mature from immature blood cells
• To assess morphology of the blood cells
• To perform manual differential count

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2
Q

AS THE BLOOD CELL MATURES…

A

Chromatin Pattern

Nucleoli

N:C Ratio (Nucleus:Cytoplasm Ratio)

Cell Size

Cytoplasmic Basophilia

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3
Q

RECALL QUESTION: What is the most reliable indicator of maturity?

A

Chromatin pattern

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4
Q

RBC MORPHOLOGY
• Normal size of RBC:
• Normal RBC shape:
• Normal RBC color/pallor:

A

RBC MORPHOLOGY
• Normal size of RBC: 6-8 um in diameter
• Normal RBC shape: Discocyte / Biconcave Disc
• Normal RBC color/pallor: 1/3 central pallor

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5
Q

Variation in the size of RBCs

A

ANISOCYTOSIS

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6
Q

Anisocytosis can be assessed using

A

RDW (Red Cell Distribution Weight)

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7
Q

MACROCYTES diseases ( ↑ MCV)

A

• Megaloblastic Anemia
• Liver Disease
• Shift Cells

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8
Q

MICROCYTES ( ↓ MCV)

A

• Iron Deficiency
Anemia (IDA)
• Thalassemia
• Chronic Blood Loss
→ Due to
gastrointestinal
bleeding

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9
Q

Major site of hematology

A

Bone marrow:

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10
Q

Parameter that will give an idea if there are macrocytes present

A

MCV

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11
Q

Variation in the shape of RBCs

A

POIKILOCYTOSIS

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12
Q

Variation in the color/pallor of RBCs

A

ANISOCHROMIA

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13
Q

Hematopoietic stem cell marker:

A

CD34

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14
Q

Regulated by erythropoietin, which is produced by the

A

kidneys

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15
Q

Main site of adult hematopoiesis or blood cell production are the following:

A

→ Vertebrate
→ Ribs
→ Sternum
→ Skull
→ Proximal ends of the femur and humerus

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16
Q

• “Spur cells”
• Large, irregular, blunt projections

A

Acanthocyte

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17
Q

Acanthocyte Found in patients with:

A

→ Abetalipoproteinemia (Bassen–Kornzweig
Syndrome)
→ McLeod phenotype (Kell Blood Group System)
▪ Rare phenotype

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18
Q

• “Burr cells”
• Projections are not as big as acanthocytes
• Spicules are more pointed and evenly distributed

A

Echinocytes

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19
Q

Echinocytes seen in

A

RECALL QUESTION: Seen in:
→ Uremia
→ Kidney problems

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20
Q

Teardrop RBCs

A

Dacrocytes

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21
Q

Dacrocytes Found in cases of:

A

Myeclotibosis / Myeloid metaplasia

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22
Q

“Sickle cell”
• Crescent, Banana shaped

A

Drepanocytes

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23
Q

Drepanocytes seen in

A

Hbs positive individuals

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24
Q

Hemolyzed RBC fragments / Debris

A

Schizocytes

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25
Schizocytes Found in
→ Hemolytic anemia → Burns
26
Horn-like / Helmet-like RBC
Keratocytes
27
Keratocytes Found in:
Hemolytic Anemia
28
Mouth-like or slit-like appearance on top view; bowl-like appearance on side view since it has a depression and not an opening
Stomatocytes
29
Stomatocytes Seen in:
Hereditary stomatocytosis Individuals with liver disease Rh null phenotype
30
Target cells; Mexican hat cell → Dartboard appearance since it has an alternating RBCs take in without staining characteristics. ▪ Dartboard appearance is due to the multiple curves of the codocytes
Codocytes
31
Codocytes seen in
→ Thalassemia → Hemoglobinopathy
32
Ovalovutes are seen in
→ Parasitic Infection ▪ Plasmodium infections (P. ovale) → Megaloblastic anemia
33
Which poikilocyte is found on a. Macrocyte b. Macro-ovalocyte
B
34
• RBCs that lacks central pallor
Spherocytes
35
Spherocytes conditions
Conditions: → Hereditary spherocytosis → Autoimmune hemolysis anemia (AIHA) → HDN - ABO shows the presence of spherocytes → HTR
36
Made up of DNA fragments
Howell Jolly bodies
37
Howell Jolly bodies test
Feulgen stain positive
38
Howell Jolly bodies Seen in condition in patients with:
Megaloblastic Anemia (Impaired DNA synthesis)
39
• Denatured Hgb • Supravital stain (Crystal violet)
Heinz bodies
40
Heinz bodies are found in
• Found in people with G6PD deficiency • Unstable Hgb → People with sensitive Hgb • Oxidizing agent (naphthalene balls)
41
• Siderotic granules (iron granules) • Demonstrated by Perl’s Prussian blue stain
Pappenheimer bodies
42
Seen in Sideroblastic anemia
Pappenheimer bodies
43
Aggregates of ribosomes
Basophilic stippling
44
Basophilic stipplingg is seen in
Seen in lead poisoning and pyrimidine 5-nucleotidase deficiency → Both conditions are board exam recall questions
45
Remnants of mitotic spindle fibers
Cabot rings
46
Reddish-violet in color, figure 8 or infinity appearance
Cabot rings
47
Cabot rings are seen in
Megaloblastic anemia
48
Seen in patients with Megaloblastic Anemia:
→ Macroovalocytes → Howell-Jolly Bodies → Cabot Rings
49
Stain for polychromasia
Polychromasia – If you applied a Wright’s stain.
50
• Increases in acute infections → Sudden onset
NEUTROPHIL
51
• Most predominant WBC in blood • Has 3-5 lobes with fine lilac granules
NEUTROPHIL
52
• Most predominant WBC in blood • Has 3-5 lobes with fine lilac granules
NEUTROPHIL
53
• Most predominant WBC in blood • Has 3-5 lobes with fine lilac granules
NEUTROPHIL
54
• Has orange-red granules; lobulated • Suppresses allergic reactions
EOSINOPHIL
55
Least common WBC in the circulation: 0-1% → Deep purple granules (Major components: Heparin & Histamine)
BASOPHIL
56
• Ground glass appearance • Horseshoe shaped nucleus
MONOCYTE
57
Largest WBC that is normally found in the blood
MONOCYTE
58
• Smallest WBC, second most predominant • Increased in most cases of viral infection
LYMPHOCYTE
59
LYMPHOCYTE
Bacterial infections that can cause Increased lymphocyte (Lymphocytosis) → Pertussis (whooping cough, Bordetella pertussis) → Tuberculosis (Mycobacterium tuberculosis) → Brucellosis
60
3 types of Lymphocytes
→ T cell → B cell → NK cell or null lymphocyte/ LGL (Large granular lymphocyte)
61
3 types of Lymphocytes
→ T cell → B cell → NK cell or null lymphocyte/ LGL (Large granular lymphocyte)
62
• Mediators of immune response; antibody production • Robin egg blue cytoplasm, compact nucleus
LYMPHOCYTE
63
Hyposegmentation; <3 lobes
PELGER-HUET ANOMALY
64
Bilobed or pince-nez appearance (eyeglass)
PELGER-HUET ANOMALY
65
>5 lobes; found in megaloblastic anemia
HYPERSEGMENTATION
66
Large, thickened granules, indicate infection
TOXIC GRANULATION
67
Similar to toxic granulation; related to mucopolysaccharidosis
ALDER-REILLY BODIES
68
• Golden-brown granules • defective lysosomes
CHEDIAK-HIGASHI
69
• related to partial albinism • Bead-like inclusions
CHEDIAK-HIGASHI
70
• related to partial albinism • Bead-like inclusions
CHEDIAK-HIGASHI
71
• Similar to Dohle bodies; but found in all types of WBC
MAY-HEGGLIN BODIES
72
• Similar to Dohle bodies; but found in all types of WBC
MAY-HEGGLIN BODIES
73
• Remnants of lymphocytes • Has faded appearance
SMUDGE CELLS
74
• Remnants of lymphocytes • Has faded appearance
SMUDGE CELLS
75
Remnants of neutrophils
BASKET CELLS
76
Neutrophil with ingested nuclear body/nucleus
LE CELL
77
Monocyte with ingested nuclear body/nucleus
TART CELL
78
Crumpled tissue appearance of monocytes / macrophages.
GAUCHER CELLS
79
GAUCHER CELLS
Related to glucocerebrosidase deficiency (Gaucher disease).
80
Related to glucocerebrosidase deficiency
GAUCHER CELLS
81
Related to sphingomyelinase deficiency (Niemann-Pick disease)
FOAM CELLS
82
• Larger (more cytoplasm) and have nucleoli in their nuclei. • The cytoplasm tends to be indented by the surrounding RBCs.
ATYPICAL / VARIANT / REACTIVE LYMPHOCYTES / DOWNEY CELLS / TURK’S IRRITATION CELLS
83
• Larger (more cytoplasm) and have nucleoli in their nuclei. • The cytoplasm tends to be indented by the surrounding RBCs.
ATYPICAL / VARIANT / REACTIVE LYMPHOCYTES / DOWNEY CELLS / TURK’S IRRITATION CELLS
84
Multinucleated giant cell with owl’s eye appearance; lacunar histiocytes
REED-STERNBERG CELLS •
85
• Associated with Hodgkin’s Lymphoma
REED-STERNBERG CELLS •
86
Checks the ability of the red blood cells to take up fluid without lysing
ERYTHROCYTE OSMOTIC FRAGILITY TEST (EOFT)
87
ERYTHROCYTE OSMOTIC FRAGILITY TEST (EOFT) primary factor
Primary factor: SHAPE OF THE RBC
88
Specimen for EOFT
Specimen: Heparinized blood or defibrinated blood
89
Increased EOFT
• Spherocytes • Senile/old RBCs
90
Decreased EOFT
• Sickle cells (drepanocytes) • Target cells (codocytes/leptocytes) • Hypochromic cells • Reticulocytes
91
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