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May lyse erythrocytes
A. 10% neutral-buffered formalin
B. Bouin solution
C. both
D. neither
B. Bouin solution
Excess fixative should be removed before processing
A. 10% neutral-buffered formalin
B. Bouin solution
C. both
D. neither
B. Bouin solution
Dehydration should be started with 65%-70% alcohol
A. 10% neutral-buffered formalin
B. Bouin solution
C. both
D. neither
A. 10% neutral-buffered formalin
Should be buffered for use
A. 10% neutral-buffered formalin
B. Bouin solution
C. both
D. neither
A. 10% neutral-buffered formalin
Contain mercuric chloride
A. 10% neutral-buffered formalin
B. Bouin solution
C. both
D. neither
D. neither
The tissue shown in image A is which organ? (pg w52)
small intestine
The tissue shown in image A (pg w52) is:
well-preserved
autolyzed
mechanically damaged
overfixed
autolyzed
The problem shown in image A (pg w52) could have been prevented by:
placing the tissue in fixative sooner
handling the tissue more carefully during gross examination
decreasing the fixation time
buffering the fixative
placing the tissue in fixative sooner
The tissue component that should be present but is missing in the tissue shown in image A (pg w52) is the:
lamina propria
muscularis mucosa
epithelium
adventitia
epithelium
The pigment seen in image B (pg w52) is most likely:
iron
formalin
mercury
bile
formalin pigment
The pigment seen in image B (pg w52) could most likely be removed by treating with:
alcoholic iodine
alcoholic picric acid
dilute hydrochloric acid
running water
alcoholic picric acid
The pigment shown in image B (pg w52) most likely:
is an exogenous hematogenous pigment
is an endogenous nonhematogenous pigment
occurred during fixation with mercury
occurred during fixation with acidic formalin
occurred during fixation with acidic formalin
The pigment shown in image B (pg w52) could have been prevented by:
washing well after fixation
keeping the pH of the fixative >6.0
treating the tissue with iodine and sodium thiosulfate
substituting paraformaldehyde for the formaldehyde
keeping the pH of the fixative >6.0
The tissue in image C (pg w53) has been screened for artifactual pigment by the use of:
fluorescent microscopy
dark field microscopy
polarizing microscopy
electron microscopy
polarizing microscopy
The technique used in image C (pg w53) uses a/an:
polarizer & analyzer
halogen lamp
electron gun
oblique light
polarizer & analyzer
CONTINUE QUESTION 105 PG W53
CONTINUE QUESTION 105 PG W53