Hematology 1 Flashcards

1
Q

Tobacco can cause ____ RBC counts and plasma catecholamines and cortisol.

A

Increased

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2
Q

EDTA spray-coated plastic tube

A

K2EDTA

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3
Q

For infants <12 months old, the most appropriate skin puncture site is the ____ or _____ plantar heel surface.

A

Lateral; medial

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4
Q

Warming the skin puncture site at ___C using moist towel would increase the blood flow through the arterioles and capillaries.

A

42

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5
Q

The lancet should be at least ___ mm long in skin puncture to prevent the risk of osteomyelitis.

A

2

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6
Q

When the erythrocytes hemolyse, what is the molecule released that will give the plasma its reddish appearance?

A

Hemoglobin

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7
Q

TRUE or FALSE: An increased reticulocyte count may be found in aplastic anemia.

A

False

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8
Q

Alpha thalassemia: ____ MCV, ____ RDW

A

Decreased; increased

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9
Q

Hemolysis: ____ Hct, ____ RBC count

A

Decreased; decreased

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10
Q

Volume percentage of RBCs in the whole blood

A

Hematocrit

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11
Q

An ____ defect can be caused by mechanical destruction eg faulty heart valves, DIC; presence of schistocytes

A

Extracorpuscular

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12
Q

2 main compartments of the bone marrow

A

Vascular sinuses

Hematopoietic cords

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13
Q

Erythropoiesis occurs in the ____.

A

Erythroblastic islands

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14
Q

Megakaryopoiesis occurs in the ____.

A

Nearby sinus endothelium

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15
Q

Blood levels of EPO is ____ proportional to tissue oxygenation.

A

Indirectly

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16
Q

Pronormoblast is also known as:

A

Rubriblast

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17
Q

Basophilic normoblast is also known as:

A

Prorubricyte

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18
Q

Polychromatophilic normoblast is also known as:

A

Rubricyte

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19
Q

Orthrochromatophilic normoblast is also known as:

A

Metarubricyte

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20
Q

Helps prevent the oxidation of hemoglobin

A

G6PD

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21
Q

G6PD deficiency causes the appearance of ____ which cause dimpling in the RBC.

A

Heinz bodies

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22
Q

Heinz bodies present in the blood will be bitten by the splenic macrophages through ____.

A

Pitting

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23
Q

Derivative of hemoglobin in which the iron is oxidized to the ferric state

A

Methemoglobin/hemiglobin

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24
Q

Storage pool of iron

A

Ferritin & hemosiderin

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25
Iron transfer from the duodenal cell into the plasma is regulated by:
Hepcidin
26
TRUE or FALSE: Iron absorbed in the body is inversely proportional to the stored iron and the rate of erythropoiesis.
True
27
Second maturational stage seen in granulocyte development
Promyelocyte
28
Stage of synthesis of primary granules
Promyelocyte
29
Stage where nuclear indentation may be seen
Metamyelocyte
30
Earliest recognizable WBC precursor under the light microscope
Myeloblast
31
Steps in phagocytosis
CAEPFD
32
Acidophilic refractile globules which represents gamma globulin synthesis; predominant in multiple myeloma
Russel bodies
33
Erythrocytes found in lead poisoning exhibit coarse granules composed of ____ that are reported as ____.
Aggregated RNA; basophilic stippling
34
Usual serum iron and transferrin levels observed in patients with anemia of chronic disorders
Serum iron decreased | Transferrin decreased
35
Also known as F thalassemia
Beta thalassemia intermedia
36
Homozygous type of beta thalassemia
Cooley's anemia
37
Erythrocytes present themselves as ____ in abetalipoproteinemia.
Acanthocytes
38
Confirmatory test for PNH
Flow cytometry of CD55 and C59
39
Hereditary pyropoikilocytosis is an erythrocyte membrane defect characterized by:
Misshapen budding fragmentation cells
40
In examining a Wright stained blood smear of a patient who just had splenectomy, one will most likely find:
Howell Jolly bodies
41
Sickle cell trait: ___% HbA, ___% HbS
60; 40
42
At pH 6, this Hb migrates to the same position as Hb A2
Hb S
43
Substitution of a single amino acid residual, lysine, for glutamic acid in the 6th position from the amino terminal end of the beta chain
Hb C
44
Light-blue gray inclusions most likely observed in the cytoplasm of many bands and neutrophils of a burn patient
Dohle bodies
45
Differentiate May-Hegglin bodies from Dohle bodies
Leukopenia with thrombocytopenia & giant platelets
46
Syndrome observed in partial albinism
Chediak-Higashi
47
Anomaly characterized by mucopolysaccharidosis
Alder-Reilly
48
Abnormal WBC most commonly found in a PBS of a patient with IM
Reactive lymphocytes
49
Pince nez appearance of neutrophil
Pelger-Huet
50
Toxic granulations are most frequently seen in:
Infection Sepsis Chemical poisoning (lead)
51
Bone marrow in alpha thalassemia major usually demostrates:
Hyperplasia
52
In regulating the cell cycle, the ___ checkpoint checks the DNA for damage and makes the cell either wait for repair or initiates apoptosis.
G1
53
The ___ checkpoint checks DNA for damage and completion of replication.
S-phase
54
The ___ checkpoint takes place after DNA synthesis and verifies that replication took place without error or damage.
G2
55
Progression through the cell cycle is regulated by ___ & ___.
Cyclin; cyclin-dependent kinases (CDKs)
56
One of the first tumor suppressor genes recognized was ___ (detects DNA damage during G1).
TP53
57
Production of megakaryocytes begins during the ____ phase.
Hepatic
58
The ____ in the bone marrow provide structural support for the developing blood cells that mature within a sea of interposed mature adipocytes.
Trabeculae
59
____ are bone-forming cells and ____ are bone-resorbing cells.
Osteoblasts; osteoclasts
60
What are the two models believed to describe the fate of HSCs?
Stochastic & instructive
61
This implies that the cell's fate is determined by intrinsic and extrinsic factors
Hematopoietic inductive microenvironment
62
Protein responsible for holding organelles in proper location in the cytoplasm of RBC precursors
Vimentin
63
Digests the ribosomes in the polychromatophilic normoblast
Endoribonuclease
64
Where is the primary oxygen-sensing system of the body located?
Peritubular fibroblasts of the kidney
65
Binding of EPO to the extracellular domain of the EPOR activates ____ signal transducers.
Janus-activated tyrosine kinase (JAK2)
66
EPO induces erythroid precursors to secrete ____, which acts on hepatocytes to decrease hepcidin production.
Erythroferrone
67
____ hepcidin production allows more iron to be absorbed from the intestines to increase hemoglobin synthesis.
Decreased
68
Glucose enters the RBC through facilitated diffusion via the transmembrane protein ____.
Glut-1
69
With the absence of G6PD, erythrocytes are particularly vulnerable to ____.
Oxidative damage
70
Any disruption in transport protein function changes the osmotic tension of the cytoplasm, leading to a ____ in viscosity, & loss of ____.
Rise; deformability
71
What process initiates various energy-dependent cellular activities through signaling receptors?
Signal transduction
72
Bands migrate through SDS gel, with their velocity a property of their MW & net charge, and are identified using ____ dye.
Coomassie blue
73
Glycophorins, with abundant side chains, are stained using ____.
Periodic acid-Schiff (PAS)
74
Decreases in transmembrane protein ____ expression has been linked with hereditary spherocytosis.
Aquaporin-1