Basic WBCs Flashcards

1
Q

Why can abnormal counts occur?

A

being consumed
being destroyed
abnormal bone marrow production

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2
Q

What are the 5 neutrophil pools?

A
stem cell pool
proliferation pool
maturation pool
circulation pool
margination pool
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3
Q

Bone marrow 0-3% nucleated cells
slight basophilic cytoplasm, fine unclear chromatin, 2-4 nucleoli
azurophilic granules or nongranular

A

myeloblast

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4
Q
1-5% nucleated cells bone marrow
round to oval nucleus
chromatin clump around edges
paranuclear hof or halo
cytoplasm evenly basophilic and full of azuorphilic granules that mass 1-3 nuclei
A

promyelocyte

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5
Q

bone marrow 6-17% of nucleated cells
last mitotic stage
more chromatin, nucleoli hard to see
production of primary granules stops and production of secondary begins
slightly pink to considerable pink cytoplasm

A

myelocyte

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6
Q

bone marrow 3-20% of nucleated cells
no mitosis
indented or kidney bean shape nucleus, chromatin clumps, no nucleoli
tertiary granules, little to no basophilia

A

metamyelocyte

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7
Q

bone marrow 9-12% nucleated cells
0-5% peripheral blood
highly clumped nucleus, indentation exceeds half
tertiary granules

A

band neutrophils

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8
Q

bone marrow 7-30%
50-70% peripheral blood
2-5 lobes
pink cytoplasm with tertiary granules

A

segmented neutrophil

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9
Q

Neutrophil function

A

immunity (innate)-protects skin and mucous barrier
chemotaxis-release of primary granules
neutrophil extracellular traps
substance for B12 absorption

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10
Q

maturation of eosinophils

A
myeloblast
myelocyte
metamyelocyte
band
mature
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11
Q

Eosinophil function

A

Granules contain cytokines, chemokine, growth factors, proteins
degranulation
Immune regulation-APCs, promote proliferation of effector T-cell, regulate mast cells
Fight helminth infections
hallmark in allergic reactions

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12
Q

maturation of basophils

A

immature

mature

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13
Q

basophil function

A

minor role in allergic reactions
induce B cells to produce IgE
promote eosinophilia

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14
Q

not considered leukocytes, maturation site in tissue, effector cells of allergic reactions and inflammatory reaction

A

mast cell

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15
Q

monocyte maturation

A

monoblast
promonocyte
monocyte

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16
Q

larger than neutrophils
nucleus round, oval, kidney, indented, folded
chromatin looser
sky-blue cytoplasm

A

monocyte

17
Q

monocyte function

A

innate-recognize and destroy bacteria
adaptive-most potent APC
housekeeping
mature in tissue ot macrophage

18
Q

B-cell function

A

antibody production

antigen presentation to T cell

19
Q

T-cell function

A

CD4 helper T cell-initiate immune response

CD8 cytotoxic T cell-kill target cell

20
Q

NK cell function

A

kills certain tumor cells and virus-infected cells without prior sensitization

21
Q

dark, blue-black cytoplasmic granules

associated with inflammation, infection

A

toxic granulation

22
Q

intracytoplasmic pale blue round or elongated bodies
remnant of rough ER
associated with nonspecific bacterial infections, sepsis, pregnancy

A

Dohle Body

23
Q

small to large circular clear areas in cytoplasm

associated with septicemia, infection, auto-phagocytosis secondary to drug ingestion, acute alcoholism

A

neutrophil vacuoles

24
Q

autosomal dominant disorder affecting a protein responsible for the nucleases shape
decreases nuclear segmentation (bilobe) and coarse chromatin pattern
can affect all leukocytes

A

Pelger Huet Anomaly

25
Q

secondary to a disease like HIV, TB, mycoplasma pneumonia, severe bacterial infections, myelodysplastic syndrome, acute myeloid leukemia, chronic myeloproliferative neoplasm, severe infection
only affects neutrophils

A

Pseudo-Pelger Huet Anomaly

26
Q

greater than 5 lobes

associated with megaloblastic anemia, myelodysplastic syndrome, hereditary neutrophil hypersegmentation

A

Neutrophil Hypersegmentation

27
Q

Recessive trait
Granulocytes with large darkly staining metachromatic cytoplasmic granules composed of partially digested mucopolysaccharide
resembles toxic granulation
lacks neutrophilic, dohle body and left shift

A

Alder-Reilly Anomaly

28
Q

rare, fatal, autosomal recessive disease
abnormal fusion of granules in granulocytes, monocytes, lymphocytes and are dysfunctional
abnormal dense granules in platelets that lead to bleeding issues

A

Chediak-Higashi Syndrome

29
Q

rare, autosomal dominant platelet disorder causing variable thrombocytopenia, giant platelets and large Dohle body like inclusions in neutrophils, eosinophils, basophils and monocytes
defect in myosin heavy chain

A

May-Hegglin Anomaly