RBCs And WBCs Flashcards

1
Q

Predominant WBC in adults

A

Neutrophils

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2
Q

Neutrophils and monocytes are direct descendants of a common progenitor, known as?

A

GMP

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3
Q

Majors stimulatory cytokine for neutrophil production 

A

G-CSF

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4
Q

What is the half-life of neutrophils in the blood?

A

7 hours

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5
Q

Able to trap and kill gram-positive and gram-negative bacteria, as well as fungi?

A

NETs (Neutrophil Extracellular Traps)

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6
Q

An enzyme that exhibits bactericidal, fungicidal and viricidal properties

A

MPO

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7
Q

Lysozyme is also known as

A

Muramidase

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8
Q

And iron-binding protein that competes with bacteria for iron

A

Lactoferrin

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9
Q

The most specific cytokines for eosinophil lineage

A

IL-5

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10
Q

Circuiting half life of eosinophils

A

18 hours

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11
Q

Survival time of eosinophils in human tissues ranges from

A

2 to 5 days

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12
Q

This happens when extracellular intact granules are deposited during cell lysis

A

Cytolisis

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13
Q

A method of eosinophil degranulation, where secretary vehicles removes specific proteins from the secondary granules. These vesicles then travel to the plasma membrane and infused to empty specific proteins into the extracellular space. 

A

Piecemeal degranulation

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14
Q

Color of Charcot-Leyden crystal in: Hematoxylin, Eosin and Trichrome stain

A

Hematoxylin- Black
Eosin- Red
Trichrome stain- Purplish-red

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15
Q

Life span of basophils

A

60 hours

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16
Q

A dye that can bind with acid mucopolysaccharides in blood cells to form metachromatic complexes

A

Toluidine blue

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17
Q

Histochemically defined as a reaction product color that is considerably different from the color of the dye itself

A

Metachromasia

18
Q

An enzyme needed to breakdown lipids

A

Sphingomyelinase

19
Q

Rare autosomal recessive
Deficiency of sphingomyelinase
Splenomegaly and hepatomegaly
Characteristic cells: Pick’s cells
A MAC whose cytoplasm is swollen by many small lipid droplets

A

Niemann-Pick Disease

20
Q

Niemann-Pick Disease which is fatal by 3 yrs of age, is most commonly seen in?

A

Ashkenazi Jews

21
Q

Most common lipidoses, Aut. Recess.; defect OR deficiency in the catabolic enzyme B-glucerebrosidase

A

Gaucher Disease

22
Q

Appearance of Gaucher cell

A

Crumpled tissue paper or onion skin

23
Q

A rare hereditary condition characterized by normal granulocyte production. Nevertheless, there is impaired released into the blood leading to neutropenia. 

A

Myelokathexis

24
Q

Most common genetic disorder of WBCs; it is the failure of the neutrophil nucleus the segment
“Pince-nez” or “spectacle” form neutrophil nucleus
Autosomal Dominant

A

Pelger-Huet Anomaly aka True/Congenital PHA

25
This is an inner nuclear membrane protein; place a major role in leukocyte nuclear shape changes that occur during normal maturation
Lamin beta-receptor 
26
True or false. There is normal granulation in through PHA 
True
27
ME ratio of leukemia
10:1
28
Type of anemia usually seen in cases of acute leukemia
Normo normo
29
Most common form of childhood leukemia
Acute Lymphocytic Leukemia
30
Peroxidase stain rules out what type of leukemia?
Acute Lymphocytic Leukemia (ALL)
31
Most sensitive stain for granulocytic precursors
Sudan Black B (SBB)
32
Basic unit of Radiation
Photon
33
Part of the platelet that ultimately dileanates individual platelets during thrombocytopoeisis
Demarcation System
34
An unique phospholipid found in the inner cytoplasmic layer of the platelets which flips to the outer surface upon activation, and is the charge phospholipid surface on which 2 coagulation pathway complexes assemble 
Phosphatidylserine
35
What are the two coagulation passed away complexes that assembles at the phosphatidylserine surface?
TENASE complex and PROTHROMBINASE complex 
36
It is the cellular ultrastructural component, unique only to the platelets
Glycocalyx
37
A molecule that binds to another molecule (especially the reference to a small molecule that specifically binds to the larger molecule)
Ligand
38
What does CAM stand for?
Cell Adhesion Molecule
39
What are the Ligands of GPIa/IIa? 
Collagen Vitronectin Laminin Fibronectin
40
Deficiency of Factor V
Owren's Disease/ Parahemophilia
41
First coagulation factor to be affected by warfarin therapy
Factor VII