Ch 3 And 12 Flashcards

1
Q

the simplest, less invasive test and uses the smallest needle to simply remove cells from the area of abnormality. This is not always adequate to obtain a diagnosis, depending on the are to be biopsied.

A

fine needle aspiration

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2
Q

removes not only cells, but also a small amount of the surrounding tissue.

A

core needle biopsy

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3
Q

takes out even more surrounding tissues. It takes out some of the abnormality, but not all. The doctor will slice into the lesion and remove only a portion of it.

A

incisional biopsy

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4
Q

generally removes the entire area in question

A

excisional biopsy

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5
Q

Considered the primary technique for obtaining diagnostic full-thickness skin specimens

A

Punch biopsy

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6
Q

where small fragments of tissue are “shaved” from a surface (usually skin)

A

Shave biopsy

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7
Q

where tissue is scooped or spooned to remove tissue or growths from body cavity such as endometrium or cervical canal

A

Curettings

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8
Q

process whereby a selected tissue specimen is immersed in isotonic salt solution such as normal saline or Ringer’s solution in a petri dish or watch glass, carefully dissected with a needle and separated by direct or zigzag spread using an applicator stick.

A

Teasing or Dissociation

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9
Q

process whereby small pieces of tissue (not more than one mm. in diameter) are placed in a microscopic slide and forcibly compressed with another slide or with a cover glass

A

Squash preparation (Crushing)

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10
Q

With an applicator stick or a platinum loop, the material is rapidly and gently applied in a direct or zigzag line throughout the slide, attempting to obtain a relatively uniform distribution of secretion.

A

Streaking

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11
Q

A selected portion of the material is transferred to a clean slide and gently spread into a moderately thick film by teasing the mucous strands apart with an applicator stick. It is especially recommended for smear preparations of fresh sputum and bronchial aspirates, and also for thick mucoid secretions

A

Spreading

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12
Q

This is done by placing a drop of secretion or sediment upon one slide and facing it to another clean slide. The material disperses evenly over the surface of the two slides. The two slides are then pulled apart with a single uninterrupted motion,

A

Pull - Apart

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13
Q

This is a special method of smear preparation whereby the surface of a freshly cut piece of tissue is brought into a contact and pressed on to the surface of a clean glass slide, allowing the cells to be transferred directly to the slide for examination by Phase Contrast microscopy or staining for light microscopic study.

A

Touch Preparation (Impression Smear)

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14
Q

The process by which processed tissue, most commonly a paraffin embedded tissue, is trimmed and cut into uniformly thin slices or “sections” to facilitate studies under the microscope

A

Microtomy

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15
Q

part of microtome where the tissue is held in position.

A

block holder

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16
Q

part of microtome that is for actual cutting of tissue sections

A

Knife carrier or Knife

17
Q

Part of microtome. To line up the tissue block in proper position with the knife, adjusting the proper thickness of the tissue for successive sections.

A

Pawl, Ratchet Feed Wheel and Adjustment Screws

18
Q

Kind of microtome. For cutting serial sections of large blocks of paraffin embedded tissues.

A

Rocking microtome

19
Q

Part of microtome. For cutting PARAFFIN embedded sections.

A

Rotary microtome

20
Q

Kind of microtome. For cutting CELLOIDIN embedded sections.

A

Sliding Microtome

21
Q

Kind of microtome. For cutting UNEMBEDDED FROZEN sections.

A

Freezing microtome

22
Q

Kind of microtome. For cutting FROZEN sections

A

Cryostat or cold microtome

23
Q

Kind of microtome. For cutting sections for ELECTRON MICROSCOPY

A

Ultrathin microtome

24
Q

available in two sizes, has been used to cut small and large blocks of paraffin tissues. It is theoretically not recommended for serial sections since tissues are cut in slightly curved planes.

A

Rocking (Cambridge) Microtome

25
Q

the device operates with a staged rotary action such that the actual cutting is part of the rotary motion.

A

Rotary (Minot) Microtome

26
Q

It was originally designed for cutting sections of very large blocks (whole brain). Sections are cut in a perfectly flat plane, thereby making excellent serial tissue sections.

A

(Sliding microtome)
Base-Sledge microtome

27
Q

It was developed mainly for cutting celloidin embedded tissue blocks and is inherently more dangerous because of the movable knife, which makes it difficult to attach knife guards.

A

Standard Sliding Microtome

28
Q

It is used to cut undehydrated thin to semi-thin sections of fresh, frozen tissues, especially in instances when rapid diagnosis is required, when histological demonstration of fat is needed, when certain neurological structures are to be studied, and when sensitive tissue constituents to be studied are damaged or destroyed by heat

A

Freezing Microtome

29
Q

a refrigerated apparatus used for freezing the tissue into the block holder to the correct degree of hardness that allows for easier and faster sectioning.

A

Cryostat or Cold Microtome

30
Q

equipped with a glass or gem grade diamond knife is used to cut very thin sections (typically 60 to 100 nanometer) of tissue embedded in epoxy resin.
Sections are stained with an aqueous solution of an appropriate heavy metal salt and examined with a transmission electron microscope (TEM).

A

Ultrathin Microtome

31
Q

Rocking (Cambridge) Microtome was invented by

A

Paldwell Trefall in 1881

32
Q

Rotary (Minot) Microtome was invented by

A

Minot in 1885-86

33
Q

Sliding Microtome was developed by

A

Adams in 1789

34
Q

Freezing Microtome was invented by

A

Queckett in 1848

35
Q

is the process whereby the “burr” formed during honing is removed and the cutting edge of the knife is polished. The purpose is to polish and sharpen the cutting edge, while that of honing is to remove the irregularities from the knife.

A

Stropping

36
Q

are generally used for trimming and semi-thin sectioning of tissue blocks for electron microscopy

A

Glass knives

37
Q

are used to cut any type of resin block for electron microscopy. are brittle and expensive, but very durable, and the cutting edge must be kept clean to make it cut longer and to avoid damage during sectioning.

A

Diamond knives

38
Q

These tools are needed for handling sections during cutting, and for removing folds and creases on the sections during “floating out” in water bath.

A

Forceps (fine pointed or curved) and squirrel hair brush