Exam 2 Flashcards
1
Q
Neutrophil Precursors
Myeloblast
A
- 14-20um
- nucleus
- N:C = 4:1
- round, oval
- chromatin fine, no clumping
- 1-3 nuclei
- cytoplasm
- blue
- no granules

2
Q
Neutrophil Precursor
Promyelocyte
A
- 15-21um
- nucleus
- N:C = 3:1
- round
- slight clumping
- 1-2 nuclei
- cytoplasm
- blue
- coarse, reddish blue primary granules

3
Q
Neutrophil Precursor
Myelocyte
A
- 12-18um
- nucleus
- N:C = 2:1 or 1:1
- round, oval or flattened
- chromatin clumped
- cytoplasm
- pink with some blue
- fine, reddish pink secondary granules
- some primary granules

4
Q
Neutrophil Precursor
Metamyelocyte
A
- 10-18um
- nucleus
- N:C = 1:1
- indented kidney shape
- chromatin clumped
- cytoplasm
- clear pink
- secondary granules

5
Q
Neutrophil Precursor
Band Neutrophil
A
- 9-15um
- nucleus
- N:C = 1:1
- elongated band, horseshoe
- U or S
- chromatin clumped
- cytoplasm
- clear pink
- secondary granules

6
Q
Neutrophil Precursor
Segmented neutrophil
A
- 9-15um
- nucleus
- N:C = 1:1
- 2-5 distinct lobes
- chromatin clumped
- cytoplasm
- clear pink
- secondary granules

7
Q
Neutrophil function
A
- adherance
- migration and diapidesis
- phagocytosis
- recognition
- ingestion
- killing and ingestion
- stimulation of coagulation
- stimulation of inflammation
- production of fever
8
Q
Function of eosinophils
A
- secretory
- defense against helminth infection
- pro inflammatory
- may protect or damage host cells
- modulation of allergic reactions
9
Q
Function of basophils
A
- secretion
- mediate inflammatory response
- especially type 1 hypersensitivity reactions
- asthma, urticaria, anaphalaxis
10
Q
Neutrophil migration
A
- cytokines cause endothelial cells to express E-selectin
- neutrophils bind to E-selectin
- neutrophils roll along VEC
- chemoattractants cause
- VEC to express ICAMs
- neutrophils express B2 integrin
11
Q
Neutrophil recognition and attachment
A
- opsonins
- coat pathogens
- complement C3B
- IgG
- PAMP
- unique molecule on pathogens
12
Q
Neutrophil phagocytosis
A
- ingestion
- pseudopod extension
- engulfment
- phagosome formation
- lysosome fusion
13
Q
Neutrophil killing
A
- intracellular
- respiratory burst
- NADPH oxidase
- super oxide (O2-)
- hydrogen peroxide (H2O2)
- hydroxyl radicals (OH-, OH+)
- NADPH oxidase
- myeloperoxidase induces production of
- hypochlorite (HOCl-)
- bleach
- hypochlorite (HOCl-)
- singlet oxygen
- strongest
- respiratory burst
14
Q
Neutrophil digestion
A
- acid pH
- lysozyme
- bactericidal proteins
- lactoferrin
- hydrolytic enzymes
15
Q
Appearance of eosinophils
A
- same developmental stages as neutrophil
- 10-16um
- N:C = 1:1
- 2 to 3 distinct lobes
- chromatin clumped
- cytoplasm
- clear pink
- large red/orange specific granules

16
Q
Appearance of basophils
A
- same developmental stages as neutrophil
- 10-16um
- nucleus
- N:C = 1:1
- 2 to 3 distinct lobes
- chromatin clumped
- often obscured by granules
- cytoplasm
- clear pink
- large violet/blue specific granules

17
Q
Growth factors for monocyte development
A
- colony stimulating factors
- granulocyte/monocyte-CSF
- GM-CSF
- monocyte-CSF
- M-CSF
- granulocyte/monocyte-CSF
- interleukin
- IL-3
18
Q
Function of monocyte/macrophage
A
- macrophage is a monocyte in the tissue
- phagocytosis
- ingest and kill microorganisms
- killing of tumor cells
- direct cytolytic effect
- ingest and degrade other cellular debris
- aged erythrocytes
- activated clotting factors
- antibody/antigen complexes
19
Q
Leukocytosis
A
- increase in leukocytes
20
Q
Leukopenia
A
- decrease in leukocytes
21
Q
Neutropenia
A
- decrease in neutrophils
22
Q
Neutrophilia
A
- increase in neutrophils
23
Q
Agranulocytosis
A
absence of granulocytes
24
Q
Granulocytosis
A
increase in all granulocytes
25
Antigen independent lymphocytes
* begins with stem cells in bone marrow
* leads to development of "immune competent cells"
26
Antigen dependent lymphocytes
* B and T cells
* occurs in secondary lymph tissue
* contact with antigen causes further proliferation of cells able to interact with that antigen
27
Gene rearrangement
* genes randomly split in certain areas then recombine
* allows each cell to code for unique proteins that react with specific antigens
* T cells
* T cell receptor chain
* B cells
* immunoglobulins
28
B cell function
* humoral immunity
* proliferate and mature into plasma cells
* secrete immunoglobulins
* posses CD19, CD20, CD24 markers
* each plasma cell produces antibodies directed at a single antigen
29
T cell function
* CD2 marker is shared by all T cells
* rearrangement of TCR gene produces T cell able to react with specific antigens
* cell mediated immunity
* CD4 helper/inducer
* release factors that increase activation of other lymphocyte subsets
* CD8 and B cells
* CD8 cytotoxic/suppressor subset
* lyse cells by direct surface to surface contact
* supress immune response through negative
30
Natural killer cell function
* 15% of lymphocytes
* CD16 and CD56 positive but CD3 negative
* functions
* recognize and kill tumor cells and virus infected cells
* attack antigens with IgG attached
31
What is anemia?
* inability of blood to supply tissues with adequate oxygen
* reduction of more than 10% of the number of red blood cells
* circulating hemoglobin and red cell mass
* if destruction exceeds production
* production is impaired
* compensating for anemia
* increased oxygenated blood flow
* increased oxygen release
32
Anemia patient symptoms
* fatigue, weakness, vertigo, syncope, dyspnea (SOB), headache
* physical exam
* pallor
* skin
* heart abnormalities
* tachycardia
* hypotension
* organomegaly
* liver or spleen
* bruising
33
**Red cell indices**
Rule of three
* Hgb x 3 = Hct
* RBC x 3 = Hgb
34
**Red cell indices**
MCV
* average volume of red cells in femtoliters
* Hct in L/L = MCV = (hct/RBC)x1000
* Hct in % = MCV = (hct/RBC)x10
* reference interval
* 80 to 100 fL
35
**Red cell indices**
MCH
* average weight of hgb in a red cell in picograms
* hgb in g/dL = MCH = (hgb/RBC)x10
* reference range
* 28 to 34pg
36
**Red cell indices**
MCHC
* comparison of weight of hgb to volume of cell
* Hct in % = MCHC = (hgb/hct)x100
* reference interval
* 32 to 36g/dL
37
Normocytic
80 to 100fL
38
Microcytic
\<80 fL
39
Macrocytic
\>100fL
40
Normochromic
32 to 36g/dL
41
Hypochromic
\<32 g/dL
42
Hyperchromic
\>36 g/dL
43
What is RDW?
* expression of variance in red cell volume
* high RDW indicates anisocytosis
* variation in red cell size
44
Bone marrow response to anemia
* reticulocyte count indicates level of bone marrow activity
* high count = high activity
45
**Classification of anemia**
By onset
* hereditary
* hemoglobin S disease
* thalassemia
* aquired
* iron deficiency
* aplastic anemia
46
**Classification of anemia**
Morphology
* microcytic
* MCV decreased
* iron deficiency
* thalassemia
* macrocytic
* MCV increased
* Vitamin B12 deficiency
* liver disease
* normocytic
* hemoglobin S disease
* aplastic anemia
47
**Classification of anemia**
MCV and RDW
* MCV decreased, RDW normal
* thalassemia minor
* MCV increased, RDW increased
* vitamin B12 deficiency
* folate deficiency
* MCV normal, RDW increased
* hemoglobin S disease
48
Iron cycle
* normal
* enteric absorption = through gut
* 1mg/day
* bone marrow uses the most iron
* storage in liver
* loss through urine, sweat, bile, ect

49
Hepcidin
* master iron regulating protein
* regulates iron recycling/balance
* inhibits activity of genes involved in iron absorption
* increased hepcidin = decreased iron absorption
* made in liver
50
Transferrin
* transports iron found in blood
* each transferrin can bind 2 irons
* binds to receptors on developing erythrocytes
* increases in response to increased need of iron
* measured transferrin = # of molecules
* TIBC = # of iron binding sites
51
Transferrin receptor (TfR)
* receptors on developing cells that receive iron and bring it into the cell
* released into the plasma as cell matures
* measurement can assess the rate of erythropoiesis in bone marrow
52
Ferritin
* iron storage in liver
* serum levels directly proportional to tissue levels
53
Hemosiderin
* iron storage
* used when levels exceed ferritin capacity
* not measurable in blood
54
Causes of iron deficiency
* chronic blood loss
* abnormal menstrual flow
* ulcers
* malignancies
* parasitic infections
* intravascular hemolysis
* hemodialysis
* dietary deficiency
* inadequate intake
* increased physiologic need
* growth, pregnancy, lactation
* malabsorption
55
Symptoms of iron deficiency
* koilonychia
* spoon nails
* glossitis
* sore tongue
* cheilitis
* sore lips
* cravings
* pica
* chills
* gastritis
56
Morphology of Iron deficiency anemia
* microcytes
* hypochromia
* elliptocytes
* target cells
57
Transferrin saturation (%TS)
* serum iron divided by TIBC x 100
58
Unsaturated iron binding capacity
UIBC
TIBC - serum iron
59
Stages of iron deficiency
* ferritin is the first to show abnormalities
* stage 3
* hemoglobin
* decreased
* MCV, MCHC
* decreased
* serum iron
* decreased
* TIBC
* increased
* %TS
* decreased
* Ferritin
* decreased
60
Serum transferrin receptor
sTfR
can differentiate IDA from ACD
61
What are hemoglobinopathies?
* genetic defect
* substitution of amino acid
* deletion of amino acid
* over 900 alterations
* effects
* altered solubility
* Hb S and Hb C
* altered function
* Hb M
* altered stability
62
Hemoglobin electrophoresis
* medium
* cellulose acetate
* pH
* 8.6
* Hb A1 = fastest
* Hb A2 = slowest
* Hb C migrates with A2
* Hb S, D, G migrate between A2 and F
* A1, F, S, C, and A2
63
Prevalance of Hb S and C
* Hb S
* 8-10% of african americans carry the gene
* 0.3-1.3% are homozygous
* Hb C
* 2-3% of african americans carry the gene
* 0.02% have the disease
64
**Globin chain defects**
Hemoglobin S
* defect of beta-globin
* substitution of valine for glutamic acid in position 6
* changes electrical charge and allows polymerization
65
**Globin chain defects**
Hemoglobin C
* defect of beta-globin
* substitution of lysine for glutamic acid in position 6
* changes electrical charge allowing polymerization
66
Clinical findings associated with SCD and trait
* chronic moderate to severe anemia caused by extravascular hemolysis
* hemolytic crisis
* increased hemolysis
* aplastic crisis
* bone marrow temporarily shuts down
* vaso-occlusive crisis
* capillaries plugged by abnormal cells
* infection
* spenic sequestration
* pooling of damaged cells in spleen
* chest syndrome
67
**Abnormal test results**
Hb S disease
* Hb
* 6-10g/dL
* severe anemia
* MCV and MCHC
* normal
* RDW
* increased
* Morphology
* target cells, sickle cells, NRBCs
* White cells and platelets
* increased
* increased reticulocytes
* 10-20%
* Hb S solubility test
* positive
* electrophoresis
* positive for hb S
* 85-100%
* increased hb F
68
**Abnormal test results**
Hb S trait
* CBC
* Hb level usually normal
* morphology
* few target cells
* Hb S solubility test
* positive
* electrophoresis
* Hb A
* 50-65%
* Hb S
* 35-45%
69
**Abnormal test results**
Hb C disease
* mild anemia
* 8-12g/dL
* morphology
* target cells, hb C crystals
* slightly increased reticulocytes
* electrophoresis
* Hb C
* \>90%
* Hb F
* \<7%
70
**Abnormal test results**
Hb C trait
* target cells
* electrophoresis
* Hb C
* 30-40%
* Hb A1
* 60-70%
71
**Abnormal test results**
Hb SC disease
* mild to moderate anemia
* 10-14g/dL
* morphology
* target cells
* SC crystals
* solubility test
* positive
* electrophoresis
* Hb S and Hb C equal amounts
* increased Hb F
* up to 70%
72
**Abnormal test results**
Hb E
* microcytes and target cells
* slight erythrocytosis
* hypochromic
* electrophoresis
* 30-40& Hb E
73
**A-thalassemia**
Major
* (--/--)
* Hb Bart's
* no functional genes
* incompatible with life
* 4 gamma chains form hb Barts
* binds but does not release oxygen
* extreme anemia present at birth
* 3-10g/dL
* 80-90% barts
* up to 20% portland
74
**A-thalassemia**
Intermedia
* (--/-a)
* Hb H disease
* excess beta chains form hb H
* anemia not as severe as major
* occasional transfusion
* no iron overload
* splenomegaly, hepatomegaly, bone deformities
* moderate anemia
* 8-10g/dL
* morphology
* microcytic, hypochromic
* target cells
* NRBCs
* increased reticulocytes
* 5-10%
* electrophoresis
* 25-40% hb barts
* 2-40% hb H
75
**A-thalassemia**
Minor
* (--/aa) or (-a/-a)
* trait
* slight to no anemia
* 10-12g/dL
* morphology
* microcytes, hypochromia, target cells, elliptocytes, basophilic stippling
* electrophoresis
* 5-6% hb barts at birth
* normal pattern in adults
76
**A-thalassemia**
Silent carrier
* (aa/a-)
* no symptoms
* MCV may be slightly abnormal
* 78-80fL
* electrophoresis
* 1-2% barts at birth
77
**B-thalassemia**
Major
* (B0/B0), (B0/B+), (B+/B+)
* 2 abnormal genes
* little to no Hb A1 produced
* increased production of delta and gamma chains
* severe anemia
* 3-4g/dL
* morphology
* microcytic and hypochromic
* MCV
* 50-60fL
* target cells, tear drop cells, elliptocytes, basophilic stippling, NRBCs
* reticulocytes increased
* 1-8%
* electrophoresis
* adult
* 0-30% hb A1
* 60-95% Hb F
* hb A2 may be normal, increased or decreased
* newborns
* \<2% hb A1
* serum bilirubin increased
* iron studies
* serum iron = increased
* TIBC = normal to increased
* %TS = \>80%
* ferritin = increased
* zpp = normal
* bone deformities
* hepatomegaly and splenomegaly
* high risk of infection
* iron overload
78
**B-thalassemia**
Minor
* (B0/B0), (B/B+)
* asymptomatic unless stressed
* mild anemia
* Hb 9-14g/dL
* MCV/MCHC low
* 55-70fL/29-33
* hypochromic, target cells, elliptocytes, basophilic stippling
* electrophoresis
* slightly elevated Hb A2
* 3.5-7.0%
* normal or slightly increased Hb F
* 1-5%