HISTOPATHOLOGIC TECHNIQUES AND PROCEDURES Flashcards
memorization
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
HISTOPATHOLOGY
Deals with the preparation of tissues for microscopic examination
HISTOPATHOLOGIC TECHNIQUE
Three post-mortem changes:
- Autolysis
- Putrefaction
- Decomposition
The destruction of the tissues by enzymes which are produced by the tissues and eventually liquefy it
autolysis
The decomposition of organic matter under the influence of microorganisms accompanied by the development of disagreeable odors
Putrefaction
Also known as degeneration; is a retrogressive process in cells in which the cytoplasm undergoes deterioration while the nucleus is preserved
Decomposition
Removal of a tissue sample from a living organism to be examined under a microscope to diagnose diseases
BIOPSY
TYPES OF BIOPSY SPECIMEN:
- Fine needle aspiration
- Core needle biopsy
- Incisional biopsy
- Excisional biopsy
- Punch biopsy
- Shave biopsy
- Curettings
SIMPLEST, LEAST INVASIVE test and uses the smallest needle to remove cells from the area of abnormality
Fine needle aspiration
Removes NOT ONLY CELLS, but also a small surrounding tissue. This provides additional information to assist in the examination of the lesion
Core needle biopsy
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
INCISIONAL BIOPSY
Removes the ENTIRE AREA in question
EXCISIONAL BIOPSY
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
PUNCH BIOPSY
Small fragments of tissue are “SHAVED” from a surface
SHAVE BIOPSY
Tissue is SCOOPED OR SPOONED to remove the tissue or growth from the body cavity such as endometrium or cervical canal
CURETTINGS
THREE METHODS OF FRESH TISSUE EXAMINATION
- TEASING OR DISSOCIATION
- SQUASH PREPARATION OR CRUSHING
- SMEARING
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
SQUASH PREPARATION OR CRUSHING
Techniques useful in CYTOLOGICAL EXAMINATIONS particularly for cancer diagnosis`
SMEARING
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
TEASING OR DISSOCIATION
FOUR (4) SMEARING TECHNIQUES FOR FRESH TIISSUE EXAMINATION **for cancer diagnosis*
- Streaking
- Spreading
- Pull-apart
- Touch preparation
Use of an applicator stick or platinum loop applied in a DIRECT OR ZIGZAG LINE
STREAKING
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
SPREADING
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
Pull-apart
Freshly cut tissue is brought into CONTACT ADN PRESSED on the surface of a clean glass slide
TOUCH PREPARATION
For RAPID DIAGNOSIS;
FROZEN SECTION
The tissue for frozen section should be sent to the laboratory FRESH and _____
UNFXED
Applications of Frozen section in Histotechnology:
- RAPID PATHOLOGIC DIAGNOSIS during surgery (PRIMARY)
- DEMONSTRATION OF LIPID (FAT CELLS) and carbohydrates (SECONDARY)
Generally, most widely used in histochemistry and during intraoperative procedures, and is the most rapid of the commonly available freezing agents
LIQUID NITROGEN
The fixative of choice for TOUCH PREPARATION:
95% Isopropyl alcohol
Primary application of frozen section:
Rapid diagnosis; TAT: 5-15 minutes
This is an excellent method for freezing MUSCLE TISSUE
ISOPENTANE
Commonly used in COLD KNIFE procedure
CAROBON DIOXIDE GAS
Used for freezing SMALL pieces of tissue except muscle
AEROSOL SPRAYS
METHODS OF PREPARING FROZEN SECTIONS:
- COLD KNIFE PROCEDURE
- CYROSTAT PROCEDURE/COLD MICROTOME
Cold knife procedure temperatures:
- KNIFE =
- TISSUE =
- ENVIRONMENT =
Cold knife procedure temperatures:
- KNIFE = -40 to -60C
- TISSUE = -5 to -10C
- ENVIRONMENT = 0 to -10C
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
CRYOSTAT PROCEDURE/COLD MICROTOME
Cryostat/Cold microtome optimum temperature =
Cryostat/Cold microtome optimum temperature =
-18 to -20C