Histopathology ang Cytologic Techniques Moving Exam

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Last updated 5:45 AM on 5/11/26
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64 Terms

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"Histo" means

tissue

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"Pathos" means

suffering

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"Logos" means

study

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<p></p>

microtome

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paraffin oven

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microtome knife

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tissue cassette

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coplin jar

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tissue floatation bath

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embedding mold

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forceps

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mature superficial cell

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intermediate cells

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parabasal cells

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navicular cell

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pregnancy cell

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endocervical glandular cell

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endometrial cells

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-The tissue is immersed in isotonic solution in a watch glass and carefully dissected with a needle and separated using an applicator stick. -It is examined unstained or stained.

Teasing or Dissociation

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-Small pieces of tissue is placed in a slide and forcibly compressed with another slide or a cover glass. -A supravital dye is added if necessary.

Squash Preparation (Crushing)

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-USing anapplicatorstick or wire loop, thematerial is rapidlyandgently appliedinadirector zogzag linethroughout theslide.

Streaking

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A selected portion of the material is transferred to a clean slide and mucus strands teased apart with an applicator stick leaving a moderately thick preparation on the slide

Spreading

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-Done by placing a drop of secretion or sediment upon one slide and facing with another clean slide. it is then pulled apart in opposite directions ensuring a uniform distribution of specimen onto both slides.

Pull-Apart

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-Surface of freshlycutpiece of tissueis broughtinto contact andpressedon to a surfaceof acleanglass slide.

TouchPreparation

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<p>what is this ? what is the temp of this device and its optimum working temp.</p>

what is this ? what is the temp of this device and its optimum working temp.

Cryostat

-10 to -20’C

optimum temp: -18 to -20’C

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state the conventional tissue processing

Fixation

Decalcification

Dehydration

Clearing

Impregnation

Embedding

Trimming

Section-Cutting

Staining

Mounting

Labeling

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what is the ratio of fixative to specimen >

20:1

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Main Factors Involved in Fixation

volume

hydrogen ion conc.

Temp.

Thickness of section

osmolality

Duration of fixation

Time interval

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two basic mechanism involved in fixation

Additive Fixation

Non-additive Fixation

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give Microanatomical Fixatives

10% formal saline

10% neutral buffered formalin

Heidenhain 's Susa

Zenker 's solution

Zenker-formal (Kelly 's solution)

Bouin's solution

Brasil's solution

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give nuclear fixatives

Flemming's fluid

Carnoy's fluid

Bouin's fluid

Newcomer's fluid

Heidenhain's Susa

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give cytoplasmic fixatives

Flemming's fluid without acetic acid

Kelly's fluidFormalin with "post-chroming"

Regaud 's fluid (Muller 's fluid)

Orth 's fluid

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give histochemical fixatives

Formal Saline 10%

Absolute Ethyl Alcohol

Acetone

Newcomer's Fluid

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most commonly used in routine histology for fixation

10% neutral buffered formalin

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in fixation,

black to brown deposits seen in tissue under the microscope.??

it can be removed by ?

acid formaldehyde hematin

can be removed by alcoholic KOH

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ratio of dehydrating agent and tissue

10:1

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most commonly used clearing agent

xylene

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in clearing what will happen if theres incomplete dehydration

it will turns milky

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xylene substitutes includes:

toluene

terpenes

limolene

orange oil

coconut oil

bleached palm oil

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melting point of paraffin wax in routine work is ?

56’C

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paraffin oven is maintained at a temp of ?

55-60’C

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give types of impregnating media

paraffin

celloidin

gelatin

plastic

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substitute of paraffin wax

paraplast 56-57’C

Embeddol 56-58’C

Esterwax 46-48’C

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Methods of Impregnation

Manual Processing

Automatic Tissue processing

Vacuum Embedding

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h & e staining

nuclei

blue to blue black

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h & e staining

karyosome

dark blue cytoplasm

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h & e staining

proteins in edema fluid

pale pink

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h & e staining

RBC, Eosinophilic granules, keratin

bright orange red

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h & e staining

basophil cytoplasm, plasma cells, osteoblast

purplish pink

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h & e staining

cartilage

pink or light blue to dark blue

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h & e staining

calcium and calcified bone

purplish blue

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rocking (cambridge) microtome

inventor:

year:

paldwell trefall

1881

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rotary microtome

inventor:

year:

MInot

1885-56

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sliding microtome

inventor:

year:

Adams

1789

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Freezing microtome

inventor:

year:

queckett

1848

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Types of Microtome knives and their lengths

Plane Concave - 25mm in length

Biconcave - 120mm in length

Plane Wedge - 100mm

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microtome knives angle and degree

Clearance angle 5-15’

wedge angle 15’

bevel angle 27-32’

rake angle 90’

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microtome parts

block holder

knife carrier and knife

pawl, ratchet feedwheel and adjustment screws

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disposable molds

peel-away

plastic ice trays

paper boat

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types of honing device

belgium yellow

arkansas

fine carborundrum

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give aqueous media

apathy’s medium

farrant’s medium

glycerin jelly

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resinous media

canada balsam

DPX

Clarite

XAM

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indirect stain

mordant

potassium alum

ehrlich’s hematoxylin

iron-weigert hematoxylin

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indirect stain

accentuator

KOH-loefflers methylene blue

Phenol-carbon thionine

fuschin