wk 1-3 Flashcards

1
Q

Function: Cuts thin sections of paraffin-embedded tissue blocks.

A

microtome

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2
Q

Contribution: Provides uniform, thin slices of tissue, which are essential for microscopic examination and accurate diagnosis.

A

microtome

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3
Q

Function: Automates the process of dehydrating, clearing, and embedding tissue samples in paraffin.

A

tissue processor

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4
Q

Contribution: Ensures consistent and efficient processing of tissue samples, preparing them for embedding and sectioning.

A

tissue processor

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5
Q

Function: Melts and molds paraffin around tissue samples.

A

Embedding Station

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6
Q

Contribution: Facilitates the embedding of tissue in paraffin blocks, which are necessary for cutting into thin sections.

A

Embedding Station

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7
Q

Function: Applies various dyes and stains to tissue sections to highlight different cellular components and structures.

A

Staining Systems (e.g., Automatic Stainers)

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8
Q

Contribution: Enhances tissue contrast and allows for visualization of specific features, aiding in the diagnosis.

A

Staining Systems (e.g., Automatic Stainers)

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9
Q

Function: Applies a coverslip to stained tissue sections mounted on slides.

A

Coverslipper

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10
Q

Contribution: Protects the stained tissue sections and provides a clear surface for microscopic examination.

A

Coverslipper

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11
Q

Function: Magnifies and visualizes tissue sections for detailed examination.

A

Microscope

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12
Q

Contribution: Allows pathologists to observe cellular and tissue structures, diagnose diseases, and assess the severity of conditions.

A

Microscope

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13
Q

Function: Cuts frozen tissue sections for immediate analysis.

A

cyrostat

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14
Q

Contribution: Enables the rapid preparation of tissue sections for intraoperative consultations and some specialized studies.

A

Cryostat

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15
Q

Function: Maintains slides at a specific temperature to prevent distortion or damage.

A

Histology Slide Warmer

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16
Q

Contribution: Ensures that tissue sections remain in optimal condition during staining and analysis.

A

Histology Slide Warmer

17
Q

Function: Melts paraffin wax used for embedding tissue samples.

A

Paraffin Bath

18
Q

Contribution: Provides a controlled temperature environment for melting and maintaining paraffin in a liquid state.

A

Paraffin Bath

19
Q

Function: Cleans slides and glassware used in histological procedures.

A

Washing Stations

20
Q

Contribution: Ensures that all equipment is free of contaminants and residues, which is crucial for accurate staining and analysis.

A

washing station

21
Q

Function: Digitizes tissue slides for digital analysis and storage.

A

Slide Scanner

22
Q

Contribution: Facilitates remote consultations, archival of samples, and integration with digital pathology systems for enhanced analysis.

A

Slide Scanner

23
Q

Function: Provides a controlled environment to protect users from exposure to hazardous materials and to prevent contamination of the samples

A

Biosafety cabinet

24
Q

Contribution: Ensures that potentially infectious or hazardous substances are contained within the cabinet, safeguarding both the technician and the integrity of the samples.

A

bsc

25
Q

aim of Histopathological technique

A

The aim is to preserve the microscopic anatomy of the tissue and make iy hard to that the section can be made

26
Q

describes the various steps required to take the tissue from fixation to the state where it is completely infiltrated with a suitable histological wax and can be embedded ready for section cutting on the microtome.Once the tissue has been fixed, it must be processed into a form in which it can be made into thin microscopic sections.

A

tissue processing

27
Q

tissue processing in order to

A

n order:
Fixation
Decalcification (optional)
Dehydration
Clearing
Impregnation (Infiltration)
Embedding
Trimming
Section-Cutting (Microtomy)
Staining
Mounting
Labelling

28
Q

fixation

A

Tissue is fixed to preserve its structure.
USE: Formalin or formaldehyde solution
Do asap
Formalin, usually as a phosphate-buffered solution, is the most popular fixative for preserving tissues that will be processed for paraffin embedding.
Following fixation, appropriately trimmed specimens are placed in suitable labelled cassettes (small perforated baskets) to segregate them from other specimens.
Formalin-fixed, paraffin-embedded tissues may be stored indefinitely at room temperature, and nucleic acids (both DNA and RNA) may be recovered from them decades after fixation.

29
Q

dehydration

A

Remove water from the tissue using increasing concentrations of alcohol
Use: acetone or isopropanol
Gradual replacement of water with alcohol to prevent tissue distortion.
Because melted paraffin wax is hydrophobic (not miscible with water), most of the water in a specimen must be removed before it can be infiltrated with wax
Fatty tissues such as breast or lipoma may be inadequately processed in what is normally a successful schedule for other tissues.
To ensure complete dehydration, a superior fat solvent such as acetone or isopropanol should be added before the final absolute ethanol, and chloroform or trichloroethane used as the transition solvent.

30
Q

clearing

A

Remove alcohol with a substance miscible with paraffin wax and ethanol
Common clearing agent: Xylene
Many clearing agents impart an optical clarity or transparency to the tissue due to their relatively high refractive index (makes tissue transparent)
Removes fat
In these stages, the ethanol is gradually replaced with xylene and when the tissue is embedded, the xylene will then be replaced by the molten paraffin wax

31
Q

Infiltration / impregnantion:

A

Replace clearing agent with embedding medium:
Typically, paraffin is used.
Clearing agent is completely removed from the tissue and replaced by a medium that gives firm consistency to the specimen (fills cavities in tissue)
The cleared tissue is infiltrated with a suitable histological wax (usually paraffin) which is liquid at 60°C and then allowed to cool to 20°C in order to solidify into a consistency that allows sections to be cut.

32
Q

embedding

A

Out of casting / blocking out
Encoding tissue in a medium and allowing medium to solidify
Uses paraffin wax
End product: tissue block
Embedding mould: can be made of stainless steel, ceramic, paper, plastic, or aluminium foil. )depends on microtome used for sectioning)
Double embedding is usually done

33
Q

trimming

A

Excess plastic surrounding the tissue must be trimmed away in a fashion that will yield a square or rectangular sections.
Trim the capsule while viewing under the dissecting microscope using old glass knives or knives not suitable for sectioning.
The capsule mold must be trimmed to a pyramid where the pyramid tip and sides are exposed tissue. The angle of the pyramid sides (called facets) should be about 45°.

34
Q

Section cutting/trimming

A

Uses microtome
Paraffin embedded tissues are trimmed and cut into uniformly thin slice or sections to facilitate studies under the microscope
Warm water bath removes wrinkles from sections

35
Q

Creates contrast in tissues, making them more visible in the microscope
Slides are dried at 60C
Tissue is rehydrated to prepare it for staining

A

Staining

36
Q
A