Intro to HISTO Flashcards

1
Q

is the study of the tissues of the body
and
how these tissues are arranged to constitute organs.

A

HISTOLOGY

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2
Q

Study of the tissue in order to study the
manifestation of the disease

A

HISTOPATHOLOGY

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3
Q

field of science that involves processing of tissue
to be able to study them under the microscope

A

HISTOTECHNOLOGY

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4
Q

Tissues have two interacting components:

A

Cells
and Extracellular matrix or ECM

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5
Q

supports the cells and contains the
fluid transporting nutrients to the cells, and
carrying away their wastes and secretory
products.

A

ECM

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6
Q

The most common procedure used in histologic
research

A

the preparation of tissue slices or “sections” that can be examined visually with
transmitted light.

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7
Q

are thin, flat slices of fixed
and stained tissues or organs mounted on glass
slides.

A

Histologic Sections

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8
Q

The correct visualization and interpretation of
sections in their proper three-dimensional
perspective on the slide.

A

Histologic Sections

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9
Q

plane of section that cuts in the
midline.

A

Longitudinal

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10
Q

a plane that intersects the
longitudinal axis at right angle.

A

Transverse

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11
Q

a plane that produces a round structure

A

Transverse

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12
Q

graze or only pass through the
outermost periphery.

A

Tangential

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13
Q

a plane that is neither longitudinal or transverse

A

Oblique

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14
Q

A plane that produces an oval structure

A

Oblique

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15
Q

techniques used to preserve via (37% formaldehyde) which inhibits autolysis through its own enzymes, degrades biological molecules

A

Histotechniques

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16
Q

used in biopsies

A

Histotechniques

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17
Q

Small pieces of tissue are placed in
solutions of chemicals that cross-link proteins
and inactive degradative enzymes, which
preserves cell and tissue structure.

A

Fixation

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18
Q

The tissue is transferred through a
series of increasingly concentrated alcohol
solutions, ending in 100% , which removes all
water.

A

Dehydration

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19
Q

Alcohol is removed in organic solvents
in which both alcohol and paraffin are miscible.

A

Clearing

20
Q

gives a translucent appearance

A

Clearing

21
Q

The tissue is then placed in melted
paraffin until it becomes completely infiltrated
with this substance.

A

Infiltration

22
Q

put into an oven (52-60 Celsius) to evaporate clearing solvent

A

Infiltration

23
Q

The paraffin-infiltrated tissue is
placed in a small mold with melted paraffin and
allowed to harden at room temp.

A

Embedding

24
Q

The resulting paraffin block is trimmed
to expose the tissue for sectioning (slicing) on a
microtome.

A

Trimming

25
Q

Uses a device called microtome and
can cut tissues into sections 1 to 10 micrometers
thick.

A

Sectioning

26
Q

Thin sections are mounted upon glass
slides.

A

Mounting

27
Q

Process that permit distinctions of
tissue components.

A

Staining

28
Q

a BASIC dye that stains ACIDIC parts BLUE, stains the NUCLEUS and ROUGH ER

A

Hematoxin

29
Q

an ACIDIC dye that stains BASIC parts PINK, stains the CYTOPLASM, MITOCHONDRIA and LYSOSOMES

A

Eosin

30
Q
  • Nuclei stain black or blue black.
  • Muscles stain red.
  • Collagen and Mucus stain green or blue.
  • Cytoplasm of most cells stains pink.
A

Masson’s Trichrome Stain

31
Q
  • Glycogen stains deep red or magenta.
A

Period Acidic-Schiff Reaction (PAS)

32
Q
  • Elastic fiber stain jet black.
  • Nuclei stain gray.
  • Remaining structures stain pink.
A

Verhoeff’s Stain for Elastic Tissue

33
Q
  • Erythrocytes stain red-orange.
  • Cytoplasm of liver and kidney stains pink.
  • Nuclei stain red.
  • Fibrous connective tissue, mucus, and
    hyaline cartilage stain deep blue.
A

Mallory-Azan Stain

34
Q

Mature RBC’s

A

Erythrocytes

35
Q
  • Erythrocyte cytoplasm stains pink.
  • Lymphocyte nuclei stain dark purple-blue
    with pale blue cytoplasm.
  • Neutrophil nuclei stain dark blue
  • Eosinophil nuclei stain dark blue and the
    granules stain bright pink.
  • Monocyte cytoplasm stains pale blue and
    nucleus stains medium blue.
A

Wright’s or Giemsa’s Stain

36
Q

Stain used in Blood Smears

A

Wright’s or Giemsa’s Stain

37
Q
  • Myelinated and Unmyelinated fibers and
    neurofibrils stain blue-black.
  • General background is nearly colorless.
  • Astrocytes stain black.
  • Depending on the methods used, the end
    product can stain black, brown, or gold.
A

Cajal’s and Del Rio Hortega’s Methods (Silver and
Gold Methods)

38
Q
  • Lipids in general stain black.
  • Lipids in myelin sheath of nerves stain black.
A

Osmic Acid (Osmium Tetroxide) Stain

39
Q

Reagent Material in Fixation

A

37% Formaldehyde

40
Q

Reagent Material in Dehydration

A

Ethanol

41
Q

Reagent Material in Clearing

A

Xylene

42
Q

Reagent Material in Infiltration and Embedding

A

Paraffin Wax

43
Q

Reagent Material in Sectioning

A

Glycol methacrylate

44
Q

Reagent Material in Mounting

A

Organic Solvent Based mounting media.
These are natural or synthetic resins
dissolved in benzene, toluene or xylene and
are used when a permanent mount is
required and frequently used in routine H
and E staining procedures.

45
Q

Reagent Material in Staining

A

Haematoxylin and eosin (H & E): Routine
stain

46
Q

These are natural or synthetic resins
dissolved in benzene, toluene or xylene and
are used when a permanent mount is
required and frequently used in routine H
and E staining procedures.

A

Organic Solvent Based mounting media.