Outcome 3 Flashcards

1
Q

Specimen is cut into thin, translucent tissue slices. The microanatomy is retained and the relationship of cells is still demonstrated.

A

Sectional Methods

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2
Q

Cut side of tissue is touched to the slide, forming an imprint. This is used to detect malignancies or when a microorganism is suspected.

A

Touch Preparation

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3
Q

Cells suspended in their own fluid may be examined directly using the mic.

A

Fresh Cells

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4
Q

Tissue is teased apart for examination of individual cells; mostly applicable to research.

A

Dissociation

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5
Q

Cell may be “fixed” to a slide for preservation of their appearance. Usually stained and may be mounted before examination.

A

Fluid Spread on Slide

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6
Q

Initial macroscopic examination of the specimen by a pathologist/technologist.

A

Gross Examination

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7
Q

Routinely used to examine tissue sections.

A

Brightfield Mic

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8
Q

Useful in identifying birefringent materials in tissue.

A

Polarizing Mic

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9
Q

Used in immunohistochemistry where antigens in tissue are demonstrated; can be used to identify TB.

A

Fluorescent Mic

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10
Q

Magnification of approx. 200,000 times; may be used for kidney biopsies (example).

A

Electron Mic

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11
Q

Dictate the processes a specimen goes through in a typical anatomical pathology lab.

A

Fixation – Accessioning – Gross Dissection – Processing – Embedding – Sectioning – Staining – Mounting

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12
Q

Fixation

A

Tissue is immersed in fixative immediately after collection for tissue preservation.

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13
Q

Accessioning

A

Specimen rec’d in the lab are given an accession # for specimen tracking while in lab.

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14
Q

Gross Dissection

A

Tissue is examined and clearly described for the health record; tissue is then grossed and placed into cassettes.

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15
Q

Processing

A

Tissue is chemically treated to prep it for paraffin wax embedding.

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16
Q

Embedding

A

Tissue is inlaid in paraffin wax to provide support during sectioning.

17
Q

Sectioning

A

Tissue is sliced, producing uniform, very thin slices and placed on a glass slide.

18
Q

Staining

A

Tissue is treated with dyes to enhance various components.

19
Q

Mounting

A

Tissue is preserved on slide using resin and coverslip resulting in a permanent preparation.

20
Q

Hematoxylin : Eosin

A

Cell Nuclei : Cell Cytoplasm

21
Q

This is the foundation for subsequent stages in preparation of tissue for diagnosis.

A

Fixation

22
Q

Give 5 examples of the purposes of fixation.

A

Prevent desiccation, prevent osmotic swelling and shrinkage, prevent putrefaction, prevent autolysis, tissue becomes firmer and easier to cut, tissue elements are stabilized, tissue constituents are more easily stained, refractive index of cellular components is changed

23
Q

A self-digestion caused after cell death by the action of intracellular enzymes causing the breakdown of protein and eventual cell liquefaction.

A

Autolysis

24
Q

What factors affect autolysis?

A

Temperature, cell type, and speed of decomposition is proportional to the natural metabolic activity of the tissue (increase metabolic activity, increase decomposition)

25
Q

Describe the microscopic appearance of an autolysed cell.

A

Cell nucleus is either in pyknosis (condensed), karyorrhexis (fragmented or lysed), or karyolysis (eventual disappearance). Cytoplasm is swollen and granular. Overall effect on cell is its granular with a homogenous mass with altered staining reactions.

26
Q

What is putrefaction?

A

Bacterial decomposition, often with gas prod, leading to eventual liquefaction.