HISTOPATHOLOGIC TECHNIQUES AND PROCEDURES Flashcards

memorization

1
Q

A branch of pathology that involves the examination of tissues and cells at a microscopic level to diagnose diseases and understand their underlying structural challenges

A

HISTOPATHOLOGY

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2
Q

Deals with the preparation of tissues for microscopic examination

A

HISTOPATHOLOGIC TECHNIQUE

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3
Q

Three post-mortem changes:

A
  1. Autolysis
  2. Putrefaction
  3. Decomposition
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4
Q

The destruction of the tissues by enzymes which are produced by the tissues and eventually liquefy it

A

autolysis

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5
Q

The decomposition of organic matter under the influence of microorganisms accompanied by the development of disagreeable odors

A

Putrefaction

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6
Q

Also known as degeneration; is a retrogressive process in cells in which the cytoplasm undergoes deterioration while the nucleus is preserved

A

Decomposition

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7
Q

Removal of a tissue sample from a living organism to be examined under a microscope to diagnose diseases

A

BIOPSY

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8
Q

TYPES OF BIOPSY SPECIMEN:

A
  1. Fine needle aspiration
  2. Core needle biopsy
  3. Incisional biopsy
  4. Excisional biopsy
  5. Punch biopsy
  6. Shave biopsy
  7. Curettings
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9
Q

SIMPLEST, LEAST INVASIVE test and uses the smallest needle to remove cells from the area of abnormality

A

Fine needle aspiration

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10
Q

Removes NOT ONLY CELLS, but also a small surrounding tissue. This provides additional information to assist in the examination of the lesion

A

Core needle biopsy

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11
Q

Takes out even more surrounding tissue. It takes out some of the abnormality, but not all. The doctor will slice into the lesion and remove ONLY A PORTION of it. If the lesion is found to be cancerous, further surgery may be needed to remove or excise the entire lesion

A

INCISIONAL BIOPSY

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12
Q

Removes the ENTIRE AREA in question

A

EXCISIONAL BIOPSY

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13
Q

Considered the primary technique for obtaining DIAGNOSTIC FULL0THICKNESS SKIN SPECIMEN. This technique involves the use of a CIRCULAR BLADE THAT IS ROTATED DOWN THROUGH THE EPIDERMIS AND DERMIS, INTO SUBCUTANEOUS FAT, YIELDING 3 TO 4 MM CYLINDIRCAL CORE OF TISSUE SAMPLE

A

PUNCH BIOPSY

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14
Q

Small fragments of tissue are “SHAVED” from a surface

A

SHAVE BIOPSY

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15
Q

Tissue is SCOOPED OR SPOONED to remove the tissue or growth from the body cavity such as endometrium or cervical canal

A

CURETTINGS

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16
Q

THREE METHODS OF FRESH TISSUE EXAMINATION

A
  1. TEASING OR DISSOCIATION
  2. SQUASH PREPARATION OR CRUSHING
  3. SMEARING
17
Q

Process where small pieces of tissue not more than 1 mm in diameter placed in a MICROSCOPE SLIDE and forcibly COMPRESSED with another slide or with a cover glass. VITAL DYES are placed at the slide and coverslip junction and absorbed through capillary action

A

SQUASH PREPARATION OR CRUSHING

18
Q

Techniques useful in CYTOLOGICAL EXAMINATIONS particularly for cancer diagnosis`

A

SMEARING

19
Q

Process wherein selected tissue specimen is immersed in a WATCH GLASS containing isotonic salt solution (NSS), carefully DISSECTED OR SEPARATED and examined under the microscope

A

TEASING OR DISSOCIATION

20
Q

FOUR (4) SMEARING TECHNIQUES FOR FRESH TIISSUE EXAMINATION **for cancer diagnosis*

A
  1. Streaking
  2. Spreading
  3. Pull-apart
  4. Touch preparation
21
Q

Use of an applicator stick or platinum loop applied in a DIRECT OR ZIGZAG LINE

A

STREAKING

22
Q

Materials is transferred in a clean slide and gently spread into a moderately thick film by TEASING using an applicator stick recommended for preparations of FRESH SPUTUM, bronchial aspirates and thick mucoid secretions

A

SPREADING

23
Q

Two slides are PULLED-APART with a single uninterrupted motion useful in preparation of THICK SECRETIONS such as serous fluids, conc. sputum, enzymatic lavage samples from GIT and blood smear

A

Pull-apart

24
Q

Freshly cut tissue is brought into CONTACT ADN PRESSED on the surface of a clean glass slide

A

TOUCH PREPARATION

25
Q

For RAPID DIAGNOSIS;

A

FROZEN SECTION

26
Q

The tissue for frozen section should be sent to the laboratory FRESH and _____

A

UNFXED

27
Q

Applications of Frozen section in Histotechnology:

A
  • RAPID PATHOLOGIC DIAGNOSIS during surgery (PRIMARY)
  • DEMONSTRATION OF LIPID (FAT CELLS) and carbohydrates (SECONDARY)
28
Q

Generally, most widely used in histochemistry and during intraoperative procedures, and is the most rapid of the commonly available freezing agents

A

LIQUID NITROGEN

29
Q

The fixative of choice for TOUCH PREPARATION:

A

95% Isopropyl alcohol

30
Q

Primary application of frozen section:

A

Rapid diagnosis; TAT: 5-15 minutes

31
Q

This is an excellent method for freezing MUSCLE TISSUE

A

ISOPENTANE

32
Q

Commonly used in COLD KNIFE procedure

A

CAROBON DIOXIDE GAS

33
Q

Used for freezing SMALL pieces of tissue except muscle

A

AEROSOL SPRAYS

34
Q

METHODS OF PREPARING FROZEN SECTIONS:

A
  1. COLD KNIFE PROCEDURE
  2. CYROSTAT PROCEDURE/COLD MICROTOME
35
Q

Cold knife procedure temperatures:

  • KNIFE =
  • TISSUE =
  • ENVIRONMENT =
A

Cold knife procedure temperatures:

  • KNIFE = -40 to -60C
  • TISSUE = -5 to -10C
  • ENVIRONMENT = 0 to -10C
36
Q

REFRIGERATED APPARATUS used in fresh tissue microtomy consists of an insulated ROTARY MICROTOME housed in an electrically driven refrigerated chamber and maintained at temperatures near -20C where microtome, knife, specimen and atmosphere are kept at the same temperature

A

CRYOSTAT PROCEDURE/COLD MICROTOME

37
Q

Cryostat/Cold microtome optimum temperature =

A

Cryostat/Cold microtome optimum temperature =

-18 to -20C