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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Neutrophil Precursor

Metamyelocyte

A
  • 10-18um
  • nucleus
    • N:C = 1:1
    • indented kidney shape
    • chromatin clumped
  • cytoplasm
    • clear pink
    • secondary granules
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Neutrophil function

A
  • adherance
  • migration and diapidesis
  • phagocytosis
    • recognition
    • ingestion
  • killing and ingestion
  • stimulation of coagulation
  • stimulation of inflammation
  • production of fever
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Function of eosinophils

A
  • secretory
    • defense against helminth infection
    • pro inflammatory
      • may protect or damage host cells
    • modulation of allergic reactions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Function of basophils

A
  • secretion
  • mediate inflammatory response
    • especially type 1 hypersensitivity reactions
    • asthma, urticaria, anaphalaxis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Neutrophil recognition and attachment

A
  • opsonins
    • coat pathogens
    • complement C3B
    • IgG
  • PAMP
    • unique molecule on pathogens
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Neutrophil phagocytosis

A
  • ingestion
    • pseudopod extension
    • engulfment
    • phagosome formation
    • lysosome fusion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Neutrophil killing

A
  • intracellular
    • respiratory burst
      • NADPH oxidase
        • super oxide (O2-)
        • hydrogen peroxide (H2O2)
      • hydroxyl radicals (OH-, OH+)
    • myeloperoxidase induces production of
      • hypochlorite (HOCl-)
        • bleach
    • singlet oxygen
      • strongest
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Neutrophil digestion

A
  • acid pH
  • lysozyme
  • bactericidal proteins
  • lactoferrin
  • hydrolytic enzymes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Growth factors for monocyte development

A
  • colony stimulating factors
    • granulocyte/monocyte-CSF
      • GM-CSF
    • monocyte-CSF
      • M-CSF
  • interleukin
    • IL-3
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Leukocytosis

A
  • increase in leukocytes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Leukopenia

A
  • decrease in leukocytes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Neutropenia

A
  • decrease in neutrophils
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Neutrophilia

A
  • increase in neutrophils
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Agranulocytosis

A

absence of granulocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Granulocytosis

A

increase in all granulocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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%