Histo 2 Flashcards

1
Q
  1. Connective tissue and muscular tissues
    arise from _________.
    I. Ectoderm
    II. Mesoderm
    III. Endoderm
    IV. Mesenchyme

A. I and II
B. II and III
C. I and IV
D. II and IV

A

D. II and IV

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2
Q
  1. Which type of epithelial lining is found in the lining of the digestive tract from the stomach down to the anus?

A. Simple squamous epithelium
B. Simple cuboidal epithelium
C. Simple columnar epithelium
D. Stratified cuboidal epithelium

A

C. Simple columnar epithelium

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3
Q
  1. What type of tissue lines the bladder?

A. Simple squamous epithelium
B. Simple cuboidal epithelium
C. Simple columnar epithelium
D. Stratified squamous epithelium
E. Transitional epithelium

A

E. Transitional epithelium

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4
Q
  1. What type of epithelial cells are as tall as
    they are wide?

A. Simple
B. Stratified
C. Squamous
D. Cuboidal
E. Columnar

A

D. Cuboidal

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5
Q
  1. What do you call the simple squamous epithelium that lines the blood vessels?

A. Epithelioid tissue
B. Mesothelium
C. Endothelium
D. Transitional
E. Pseudostratified

A

C. Endothelium

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6
Q
  1. Which of the following is NOT primarily composed of connective tissue?

A. Blood
B. Bone
C. Tendon
D. Intervertebral disc
E. Myometrium

A

E. Myometrium

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7
Q
  1. Which of the following is NOT a fiber found in connective tissue?

A. Collagen fiber
B. Elastic fiber
C. Reticular fiber
D. Purkinje fiber
E. All of the above are fibers found in connective tissue

A

D. Purkinje fiber

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8
Q
  1. What type of adipose tissue tends to increase as humans age?

A. Brown adipose tissue
B. White adipose tissue
C. Unilocular adipose tissue
D. Multilocular adipose tissue
E. Both b and c

A

E. Both b and c

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9
Q
  1. Which of the following would be best suited to differentiate collagen fibers from other fibers?

A. Wright’s stain
B. Hematoxylin and eosin stain
C. Sudan stain
D. Silver impregnation
E. Masson’s trichrome stain

A

E. Masson’s trichrome stain

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10
Q
  1. Which of the following stain blue with H&E stain?

A. Cytoplasm
B. Collagen fibers
C. Nucleus
D. Elastic fibers
E. Decalcified bone matrix

A

C. Nucleus

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11
Q
  1. What are Sudan stains used primarily for?

A. Blood
B. Fat
C. Nervous tissue
D. Elastic fibers
E. Decalcified bone matrix

A

B. Fat

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12
Q
  1. What is Mucicarmine stain used primarily for?

A. Blood
B. Fat
C. Nervous tissue
D. Elastic fibers
E. Epithelial mucin

A

E. Epithelial mucin

*Mucicarmine is used to see epithelial mucin.
It stains it a deep red.

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13
Q
  1. What is Wright’s stain used primarily for?

A. Blood
B. Fat
C. Nervous tissue
D. Elastic fibers
E. Decalcified bone matrix

A

A. Blood

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14
Q
  1. What color do elastic fibers stain with Verhoeff Elastic stain?

A. Red/Orange
B. Pink/red
C. Purple/Red
D. Blue/black
E. Green/blue

A

E. Green/blue

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15
Q
  1. During the preparation of a routine H&E slide, what step occurs after the tissue is preserved?

A. Fixation
B. Embedding in paraffin
C. Staining
D. Slicing
E. Dehydration

A

E. Dehydration

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16
Q
  1. During the preparation of a routine H&E slide, how is the tissue preserved?

A. Fixation
B. Embedding in paraffin
C. Staining
D. Slicing
E. Dehydration

A

A. Fixation

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17
Q
  1. During the preparation of a routine H&E slide, what allows the tissue to be visualized?

A. Fixation
B. Embedding in paraffin
C. Staining
D. Slicing
E. Dehydration

A

D. Slicing

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18
Q
  1. Which of the following would be best suited to visualize reticular fibers?

A. Wright’s stain
B. Hematoxylin and eosin stain
C. Sudan stain
D. Silver impregnation
E. Masson’s trichrome stain

A

D. Silver impregnation

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19
Q
  1. Which of the following would be best suited to visualize lipid?

A. Wright’s stain
B. Hematoxylin and eosin stain
C. Sudan stain
D. Silver impregnation
E. Masson’s trichrome stain

A

C. Sudan stain

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20
Q
  1. Ideal amount of the fixative:

A. 1 – 2X the volume of the specimen
B. 5 – 10X the volume of the specimen
C. 10 – 15X the volume of the specimen
D. 10 – 20X the volume of the specimen

A

D. 10 – 20X the volume of the specimen

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21
Q
  1. All of the following are microanatomical
    fixatives, EXCEPT:

A. 10% Formalin
B. Zenker’s solution
C. Bouin’s solution
D. Flemming’s fluid

A

D. Flemming’s fluid

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22
Q
  1. Best fixative for the nervous system:

A. Formalin fixative
B. Permanganate fixative
C. Lead fixative
D. Chromate fixative

A

A. Formalin fixative

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23
Q
  1. Fixative of choice for the preservation of fats:

A. Helly’s fluid
B. Newcomer’s fluid
C. Formalin
D. Newcomer’s fluid

A

C. Formalin

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24
Q
  1. Helly’s fluid is exactly the same as in Zenker’s fixative, but instead of GLACIAL ACETIC ACID, what component is added:

A. Mercuric chloride
B. Potassium dichromate
C. Sodium sulfate
D. Formalin

A

D. Formalin

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25
25. Fixative recommended for fixing small pieces of liver, spleen, connective tissue fibers and nuclei: A. Zenker’s fluid B. Orth’s fluid C. Heidenhain’s Susa solution D. Regaud’s fluid
A. Zenker’s fluid
26
26. Excellent microanatomic fixative for pituitary gland, bone marrow and blood containing organs such as spleen and liver: A. Bouin’s solution B. Helly’s fluid C. Carnoy’s fluid D. Flemming’s solution
B. Helly’s fluid
27
27. All mercurial fixing solutions lead to the formation in tissues of diffuse BLACK granules and these mercury deposits must be removed BEFORE STAINING. Removal of mercuric chloride deposit is accomplished by: A. Saturated solution of iodine B. Sodium thiosulfate C. Distilled water D. Saturated solution of picric acid
A. Saturated solution of iodine
28
28. Considered to be the MOST RAPID fixative/ recommended for fixing chromosomes, lymph glands and urgent biopsies: A. Gendre’s fixative B. Carnoy’s fluid C. Newcomer’s fluid D. Flemming’s solution
B. Carnoy’s fluid
29
29. Fixatives used mainly for acid mucopolysaccharides: A. Lead fixatives B. Mercurial fixatives C. Chromate fixatives D. Picric acid fixatives
A. Lead fixatives
30
30. Most widely used fixative for electron microscopy: A. Acetone B. Zenker’s fluid C. Osmium tetroxide D. Trichloroacetic acid
C. Osmium tetroxide
31
31. The process of decalcification is best performed: A. Before fixation B. After fixation C. After impregnation D. None of these
B. After fixation
32
32. Most ideal and most reliable method of determining extent of decalcification: A. Physical test B. Chemical test C. X-ray or radiological test D. Adsorption test
C. X-ray or radiological test
33
33. The fastest chemical solution in decalcifying tissues is: A. Trichloroacetic acid B. Nitric acid C. Formic acid D. Versene
B. Nitric acid
34
34. All of the following remove intracellular and extracellular water from the tissue following fixation, EXCEPT: A. Alcohol B. Chloroform C. Tetrahydrofuran D. Dioxane
B. Chloroform
35
35. A TOXIC dehydrating agent, primarily employed for blood and tissue films and for smear preparation: A. Ethyl alcohol B. Methyl alcohol C. Butyl alcohol D. Isopropyl alcohol
B. Methyl alcohol
36
36. Function/s of tetrahydrofuran: A. Dehyrating agent B. Clearing agent C. Both of these D. None of these
C. Both of these
37
37. Excessive exposure to this clearing agent may be extremely toxic to man and may become carcinogenic or it may damage the bone marrow resulting to APLASTIC ANEMIA: A. Xylene B. Benzene C. Tetrahydrofuran D. Toluene
B. Benzene
38
38. Process whereby the clearing agent is completely removed from the tissue and replaced by a medium that will completely fill all the tissue cavities: A. Embedding B. Infiltration C. Blocking D. Casting
B. Infiltration
39
39. Simplest, most common and best embedding medium for routine tissue processing: A. Paraffin wax B. Ester wax C. Celloidin D. Carbowax
A. Paraffin wax
40
40. A semi-synthetic wax used for embedding the eyes: A. Paraplast B. Bioloid C. Ester wax D. Carbowax
B. Bioloid
41
41. The DRY celloidin embedding method is employed chiefly for the: A. Bones and teeth B. Large brain blocks C. Whole organs D. Eyes
D. Eyes
42
42. All of the following are substitutes for paraffin wax, EXCEPT: A. Paraplast B. Embeddol C. Malinol D. Tissue Mat
C. Malinol
43
43. Melting point of ester wax: A. 56-57°C B. 46-48°C C. 54-58°C D. 50-54°C
B. 46-48°C
44
44. The last container through which tissue pass through in an automatic tissue processor contains: A. Paraffin B. Xylol C. Formalin D. Alcohol
A. Paraffin
45
45. Microtome knife recommended for frozen sections or for cutting extremely hard and tough specimens embedded in paraffin blocks, using a base-sledge type or sliding microtome: A. Plane-concave knife B. Plane-wedge knife C. Biconcave knife D. None of these
B. Plane-wedge knife
46
46. Removal of gross nicks on the knife edge: A. Honing B. Stropping C. Both of these D. None of these
A. Honing
47
7. Removal of “burr” or irregularities on the knife edge: A. Honing B. Stropping C. Both of these D. None of these
B. Stropping
48
48. Angle formed between the cutting edge of the microtome knife (27°-32°): A. Bevel angle B. Clearance angle C. Both of these D. Neither of these
A. Bevel angle
49
49. Angle formed between the surface of the block and the cutting edge of the knife (0°-15°): A. Bevel angle B. Clearance angle C. Both of these D. Neither of these
B. Clearance angle
50
50. This type of microtome easily cuts large blocks and serial sections can be obtained with ease because larger knives can be used: A. Sliding B. Rotary C. Rocking D. Freezing
A. Sliding
51
51. The cryostat is an apparatus used in fresh tissue microtomy. It consists of a microtome, kept inside a cold chamber which has been maintained at a temperature of: A. 20°C B. -20°C C. 4°C D. -4°C
B. -20°C
52
52. A tissue exposed to short burst of CARBON DIOXIDE for a few minutes will: A. Freeze B. Harden C. Dehydrate D. Fix
A. Freeze
53
53. Fat cells and enzymes are best demonstrated in: A. Paraffin section B. Plastic embedded section C. Celloidin section D. Frozen section
D. Frozen section
54
54. When trimming tissue block, they must be surrounded by at least __ of wax. A. 1 mm B. 2 mm C. 3 mm D. 4 mm
B. 2 mm
55
55. Thickness of paraffin sections for routine histologic procedures: A. 10-15µ B. 4-6 µ C. 0.5µ D. 5-10µ
B. 4-6 µ
56
56. The following methods are done for drying sections on slide, EXCEPT: A. On a hot plate at 45-55°C for 30-45 min. B. On a Bunsen flame C. In an incubator at 37°C for 3 hours D. In a wax oven at 56-60°C for 2 hours
C. In an incubator at 37°C for 3 hours
57
57. Most probable cause when clearing agent turns milky as soon as the tissue is placed in it: A. Incomplete fixation B. Prolonged fixation C. Incomplete dehydration D. Prolonged dehydration
C. Incomplete dehydration
58
58. It is added to Mayer’s egg albumin to prevent the growth of molds: A. Sodium chloride B. Glycerol C. Thymol crystals D. Powdered starch
C. Thymol crystals
59
59. Adhesive added to the water in the floating-out bath – most convenient alternative to direct coating of slides: A. Plasma B. Gelatin C. Starch paste D. Dried albumin
B. Gelatin
60
60. To avoid distortion of the image, the refractive index of the mountant should be near as possible to that of the glass which is: A. 1. 581 B. 1.185 C. 1.518 D. 1.155
C. 1.518
61
61. Deparaffinization of tissue sections is accomplished by passing through: A. Ammonia water B. Acetone C. Alcohol D. Xylol
D. Xylol
62
62. Coverslips from slides may be removed by immersion in: A. Ammonia water B. Acetone C. Alcohol D. Xylol
D. Xylol
63
63. Process by which sections are stained with simple aqueous or alcoholic solutions of the dye: A. Progressive staining B. Regressive staining C. Direct staining D. Indirect staining
C. Direct staining
64
64. A tissue-mordant-dye complex is needed in: A. Progressive staining B. Regressive staining C. Direct staining D. Indirect staining
D. Indirect staining
65
65. With this staining technique, the tissue is first overstained, and the excess stain is removed or decolorized from unwanted part of the tissue: A. Progressive staining B. Regressive staining C. Direct staining D. Indirect staining
B. Regressive staining
66
66. The regressive staining method employs this procedure: A. Deparaffinization B. Clearing C. Differentiation D. Dehydration
C. Differentiation
67
67. Accelerate or hasten the speed of the staining power and selectivity of the dye: A. Oxidizing agents B. Acid differentiators C. Accentuators D. Mordants
C. Accentuators
68
68. Substances which aid in attaching a stain or dye to the tissue: A. Oxidizing agents B. Acid differentiators C. Accentuators D. Mordants
D. Mordants
69
69. This technique entails the use of specific dyes, which differentiate particular substances by staining them with a color that is different from that of the stain itself: A. Orthochromatic staining B. Metachromatic staining C. Counterstaining D. Vital staining
B. Metachromatic staining
70
70. All of the following are metachromatic stains, EXCEPT: A. Thionine B. Toluidine blue C. Safranin D. Eosin
D. Eosin
71
71. Stain used for demonstrating mitochondria during intravital staining: A. Victoria blue B. Acridine orange C. Benzidine D. Janus Green B
D. Janus Green B
72
72. Application of a different color or stain to provide contrast and background to the staining of the structural component to be demonstrated: A. Orthochromatic staining B. Metachromatic staining C. Counterstaining D. Vital staining
C. Counterstaining
73
73. The routine stain for surgical tissue section is: A. Gram’s stain B. Wright’s stain C. Pap’s stain D. H&E stain
D. H&E stain
74
74. Routinely used in histopathology as a counterstain/background for contrasting stain because it gives a pleasing and colorful contrasts to nuclear stains: A. Eosin B. Toluidine blue C. Methylene blue D. Crystal violet
A. Eosin
75
75. In the hematoxylin-eosin stain (H&E), this stain acts as the acid dye: A. Hematoxylin B. Eosin C. Either of these D. Neither of these
B. Eosin
76
76. In routine H&E, most fixatives can be used, EXCEPT: A. Zenker’s formol B. Formaldehyde C. Osmic acid D. Picric acid
C. Osmic acid
77
77. Only substance in histopathology that can fix, differentiate or stain tissues all by itself: A. Osmic acid B. Picric acid C. Trichloroacetic acid D. Acetic acid
B. Picric acid
78
78. The active dye (coloring agent) in hematoxylin solution is: A. Hematin B. Hematein C. Hematoxylin D. Hematoxylon
B. Hematein
79
79. All of the following are chemical oxidizing agent/ripening agent for hematoxylin, EXCEPT: A. Sodium iodate B. Mercuric oxide C. Hydrogen peroxide D. Ammonium alum
D. Ammonium alum
80
80. Ripening agent for Harris’ hematoxylin: A. Sodium iodate B. Mercuric oxide C. Potassium permanganate D. Hydrogen peroxide
B. Mercuric oxide
81
81. Function of ammonium alum in the Harris hematoxylin formula: A. Oxidizing agent B. Mordant C. Dye solvent D. Dye
B. Mordant
82
82. Staining of the nuclei by alum hematoxylin is enhanced by the addition of: A. Alum B. Ethanol C. Glacial acetic acid D. Mercuric oxide
C. Glacial acetic acid
83
83. Glacial acetic acid added to hematoxylin will: A. Inactivate stain B. Decrease nuclear staining C. Enhance cytoplasmic staining D. Enhance nuclear staining
D. Enhance nuclear staining
84
84. A sheen of oxidized dye on the surface of hematoxylin solution indicates: A. Stain is concentrated B. Stain is contaminated by bacteria C. Stain has to be filtered D. Stain has to be discarded
C. Stain has to be filtered
85
85. Acid alcohol used in routine H&E acts as: A. Mordant B. Stain C. Bluing agent D. Differentiator
D. Differentiator
86
86. The acid used in combination with alcohol in an acid alcohol solution: A. Acetic acid B. Oxalic acid C. Nitric acid D. Hydrochloric acid
D. Hydrochloric acid
87
87. Staining result in the routine hematoxylin and eosin method: A. Nuclei pink, cytoplasm blue to blue-black B. Nuclei blue to blue-black, cytoplasm pink C. Nuclei and cytoplasm pink D. Nuclei and cytoplasm blue-black
B. Nuclei blue to blue-black, cytoplasm pink
88
88. A common BASIC NUCLEAR STAIN for plasma cells and may also be employed in cytological examination of fresh sputum for malignant cells: A. Eosin B. Methylene blue C. Crystal violet D. Aniline blue
B. Methylene blue
89
89. PAS positive substances are stained: A. Blue B. Brown-black C. Green D. Magenta red
D. Magenta red
90
90. Staining method for glycogen: A. PAS technique B. Langhan’s iodine stain C. Best Carmine method D. All of these
D. All of these
91
91. Tubercle bacilli in Ziehl-Neelsen stain: A. Bright red B. Grayish blue C. Green D. Blue
A. Bright red
92
92. Feulgen’s reaction is the most reliable and most specific histochemical staining technique for: A. RNA B. DNA C. Both D. Neither
B. DNA
93
93. In the Masson-Fontana ammoniacal silver reaction, melanin and argentaffin cell granules are stained: A. Brown B. Red C. Black D. Blue
C. Black
94
94. Lipids in Sudan IV are stained: A. Black B. Blue black C. Red D. Deep blue to violet
C. Red
95
95. Positive reaction for cholesterol in Schultz Method: A. Blue-black B. Grayish-blue C. Pale pink D. Blue-green
D. Blue-green
96
96. The method of choice for staining in exfoliative cytology: A. Pap’s stain B. Wright’s stain C. H&E stain D. Giemsa stain
A. Pap’s stain
97
97. Continuous abnormal proliferation of cells without control causes an overgrowth of tissue or tumor cells: A. Anaplasia B. Hyperplasia C. Neoplasia D. Dysplasia
C. Neoplasia
98
98. The dissolving of cells by enzymatic action is: A. Rotting B. Decay C. Autolysis D. Putrefaction
C. Autolysis
99
99. A malignant tumor is least characterized by: A. Metastases B. Mitotic figures C. Encapsulation D. Invasion of adjacent tissues
C. Encapsulation
100
100. Father of modern histology A. Rudolf Virchow B. Marie François Xavier Bichat C. Hippocrates D. Gregor Mendel
B. Marie François Xavier Bichat