HPCT MIDTERM: Exam Review Questions
Aim of clearing.
To remove calcium salts.
To remove fixative and water.
To remove dehydrating agents.
To remove excess wax.
Aim of trimming.
To remove calcium salts.
To remove fixative and water.
To remove dehydrating agents.
To remove excess wax.
Aim of decalcification.
To remove calcium salts.
To remove fixative and water.
To remove dehydrating agents.
To remove excess wax.
Aim of dehydration.
To remove calcium salts.
To remove fixative and water.
To remove dehydrating agents.
To remove excess wax.
Ideal time required for decalcification.
1-2 days
15-60 mins
14-48 hrs
2-3 days
Decalcifying agent recommended for urgent biopsies.
Formol nitric acid
5-10% nitric acid
5% formic acid
Versene
Clearing agent recommended for urgent biopsies.
Formol nitric acid
Toluene
Benzene
Phloroglucin nitric acid
Recommended for routine decalcification of postmortem research tissues.
5% formic acid
5-10% nitric acid
Electrophoresis
TCA
Decalcifying agent used for teeth and small pieces of bones.
Von Ebner
Sulfurous acid
Flemming's fluid
TCA
Decalcifying agent suitable for minute pieces of bones.
TCA
Chromic acid
Von Ebner's
Sulfurous acid
Decalcifying agent suitable for minute bone spicules.
TCA
Chromic acid
Sulfurous acid
Von Ebner's
Decalcifying agent suitable for small spicules of bones.
TCA
Chromic acid
Flemming's fluid
Sulfurous acid
DECALCIFYING AGENTS
Nitric acid
12-24 hrs
TCA
1-14 days
Formol nitric acid
4-8 days
Ion exchange resins
2-7 days
Phlroglucin nitric acid
1-3 days
5% formic acid
1-2 days
Increases tissue solubility by hastening decalcification using formic acid that contains decalcifying solution.
Ion exchange resin
Electrophoresis
EDTA
Nitric acid
Sequestration of calcium
EDTA
Versene
NOTA
AOTA
Shorter time for calcium removal.
Ion exchange resin
Electrophoresis
EDTA
Nitric acid
Which of the following statements is true about standard sliding microtome?
It is considered the most dangerous type of microtome.
It is used mainly for celloidin-embedded tissue blocks.
It is used for extremely hard tissue blocks.
It has movable and exposed knife.
All of the choices are correct
Most ideal and most sensitive method of measuring decalcification rate.
Xray
Physical
Chemical
Mechanical
Affects the rate at which calcium is removed.
Concentration
Fluid access
Size and consistency
Temperature
Agitation
The larger the specimen, the longer the decalcification time.
Concentration
Fluid access
Size and consistency
Temperature
Agitation
High corrosive and carcinogenic decalcifying agent.
TCA
Chromic acid
Sulfurous acid
Perenyi's fluid
A tissue softener that makes tissue appear swollen and soapy.
Molliflex
4% Phenol
Lendrums fluid
2% HCl
Softens tissue and allows for easier sectioning.
Molliflex
4% Phenol
2% HCl
1% HCl
Tissue to fluid volume ratio.
1:20
20:1
10:1
1:10
Dehydrating agent to tissue ratio.
1:10
1:20
10:1
20:1
Best dehydrating agent.
Ethanol
Methanol
5% formic acid
Acetone
Best general decalcifying agent.
5% formic acid
Formol nitric acid
Ethyl alcohol
Most rapid decalcifying agent.
5% formic acid
5-10% nitric acid
Phloroglucin nitric acid
Formol nitric acid
Excellent dehydrating and clearing agent.
Dioxane
5% formic acid
Tetrahydrofuran
Ethanol
Slow dehydrating agent
Butanol
Cellosolve
Acetone
Methyl alcohol
Dehydrating agent recommended for delicate tissues such as embryonic and animal tissues.
30% ethanol
4% phenol
95% ethanol
Aniline oil
Toxic fixative and dehydrating agent.
Methyl alcohol
Tetrahydrofuran
Cellosolve
Dioxane
Toxic dehydrating and clearing agent.
Methyl alcohol
Tetrahydrofuran
Cellosolve
Dioxane
Preserves negri bodies.
Acetone
Cellosolve
Ester wax
Mineral oil
Clearing agent that causes minimum shrinkage.
Clove oil
Triethyl phosphate
Cellosolve
Cedarwood oil
Used to dehydrate smears producing minimal shrinkage.
Triethyl phosphate
Clove oil
Carbon tetrachloride
Most commonly used clearing agent.
Xylol
Toluene
Aniline oil
Benzene
Serves as an indicator that dehydration is complete.
Anhydrous copper sulfate
Xylene
4% phenol
30% ethanol
Substitute for benzene or xylene
Xylol
Toluene
Aniline oil
Benzene
Noncarcinogenic clearing agent.
Xylol
Toluene
Aniline oil
Benzene
Clearing agent recommended for CNS tissue and cytology.
Clove oil
Glycerine
Carbon tetrachloride
Cedarwood oil
Similar to chloroform but cheaper.
Clove oil
Glycerine
Carbon tetrachloride
Cedarwood oil
No dealcoholization but make the tissue clearer.
Clove oil
Glycerine
Carbon tetrachloride
Cedarwood oil
Turns milky which indicates incomplete dehydration
Xylol
Cedarwood oil
Aniline oil
Benzene
Chloroform may cause ___________.
Hepatotoxicity
Conjunctival irritation
Minimum shrinkage
Tissue distortion
Best embedding medium.
Paraffin wax
Embeddol
Paraplast
Bioloid
Less brittle and less compressible than paraplast.
Paraffin wax
Embeddol
Paraplast
Bioloid
Embedding medium used for large dense tissue blocks.
Paraffin wax
Embeddol
Paraplast
Bioloid
Embedding method that is toxic and damage tissues.
Epoxy
Polyester
Acylic
Gelatin
Celloidin method used for whole organ and brain sections.
Wet celloidin
Dry celloidin
Nitrocellulose
Celloidin method used for whole eye sections.
Dry celloidin
Wet celloidin
Nitrocellulose
A form of celloidin soluble in equal concentration of ether and alcohol.
Dry celloidin
Wet celloidin
Nitrocellulose
MELTING POINTS
Lab temp 20-24C
56-57C
Ester wax
46-48C
Paraplast
56-58C
Lab temp 15-18C
50-54C
Embeddol
54-58C
TYPES OF HONES
Arkansas
Gives more polishing effect.
Fine cardorundum
For manual sharpening when cutting edge has been rendered blunt or nicked.
Belgium yellow
Much coarser and used only for badly nicked knives.
What is added to gelatin to prevent molds?
1% phenol
4% phenol
2% HCl
1% HCl
Embedding medium that is soluble and miscible with water.
Carbowax
Nitrocellulose
Paraplast
Bio/Aid
Used for embedding eye sections.
Paraffin wax
Embeddol
Paraplast
Bioloid
Process by which a processed tissue is cut into uniformly thin slices to facilitate studies under the microscope.
Embedding
Trimming
Sectioning
Stropping
What is the thickness of the tissue blocks for routine histology?
4-6 um
0.5 um
3-5 um
4 um
What is the thickness of the tissue blocks for frozen section?
4-6 um
0.5 um
3-5 um
10-15 um
What is the thickness of the tissue blocks when a cold microtome is used?
10-12 um
0.5 um
3-5 um
4 um
What is the thickness of the tissue blocks when a rotary microtome is used?
10-12 um
0.5 um
3-5 um
4 um
What is the thickness of the tissue blocks when a rocking microtome is used?
10-12 um
0.5 um
3-5 um
4 um
Both sides are concave.
Plane-wedge knife
Biconcave knife
Plane-concave knife
Recommended for cutting paraffin embedded sections on a rotary microtome.
Plane-wedge knife
Biconcave knife
Plane-concave knife
One side of the knife is flat and the other is concave.
Plane-wedge knife
Biconcave knife
Plane-concave knife
Recommended for frozen sections or extremely hard and tough specimens.
Plane-wedge knife
Biconcave knife
Plane-concave knife
Both sides are flat.
Plane-wedge knife
Biconcave knife
Plane-concave knife
How long does it take to dry processed tissue on slides using drying oven?
30 mins
60 mins
15-20 mins
15-60 mins
Which of the following statements is/are true about the purpose of honing?
To uniformly cut the sections into thin slices.
To remove the nicks from the knife.
To polish and sharpen the knife edge.
2 of the choices are correct.
Which of the following statements is/are true about the purpose of stropping?
To uniformly cut the sections into thin slices.
To remove the nicks from the knife.
To polish and sharpen the knife edge.
None of the choices are correct.
Recommended for extremely hard and rough tissue blocks.
Base sledge
Rocking microtome
Cold microtome
Standard sliding microtome
Most common type used for both routine and research labs.
Freezing microtome
Sliding microtome
Rotary microtome
Rocking microtome
Most commonly used for rapid preparation of urgent tissue biopsies for inoperative diagnosis.
Freezing microtome
Rocking microtome
Cold microtome
Standard sliding microtome
Most dangerous type of microtome.
Freezing microtome
Rocking microtome
Cold microtome
Standard sliding microtome
Simplest among the microtomes.
Freezing microtome
Ultrathin microtome
Rotary microtome
Rocking microtome
For cutting frozen sections.
Freezing microtome
Rocking microtome
Cryostat
Standard sliding microtome
For cutting sections for EM.
Sliding microtome
Rotary microtome
Ultrathin microtome
Base sledge
Cryostat
For cutting serial sections of large blocks of paraffin embedded tissues.
Freezing microtome
Sliding microtome
Rotary microtome
Rocking microtome
For cutting unembedded frozen sections.
Freezing microtome
Ultrathin microtome
Cold microtome
Base sledge
Originally made for cutting very large blocks such as whole brain.
Base sledge
Rocking microtome
Cold microtome
Standard sliding microtome
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