18.Mainly in what cells does granular dystrophy occur?
A In the cells of the kidney, liver and heart
B. In the cells of the spleen and lymph nodes
B. In the cells of the lungs and stomach
D. In the cells of bones and bone marrow.
19.Forms of spleen amyloidosis?
A Follicular and diffuse
B. Follicular and tuberculous
B. Focal and necrotic
G. Watery.
20. Specify mesenchymal dysproteinoses?
A Mucoid, fibrinoid, swelling, hyalinosis, amyloidosis
B. Fibrinoid necrosis
B. Granular, protein dystrophy
D. Pigmentary dystrophy.
21. Causes of protein dystrophy?
A Digestive disorder
B. Endogenous and exogenous
B.. Catarrhal and hemorrhagic
G.Fibrinous, necrotic.
22.Types of fatty liver?
A Fatty infiltration, fatty degeneration
B. Hydropic dystrophy
B. Catarrhal and hemorrhagic
G. Serous, fibrinous.
23. In what forms does spleen amyloidosis occur?
A B follicular and diffuse
B. In lobular, follicular
B. In lobar and lobular
G. In diffuse and lobar.
24. In what part of the liver does the development of liver amyloidosis begin?
A From the peripheral part of the hepatic lobules
B. From the reticular stroma of the hepatic lobules
B. Between Cooper cells of the liver
D. From hepatocytes.
25.What changes cause organs to decrease in size?
A For atrophy
B. For dystrophy
B. With necrosis
D. With inflammation.
26.What changes cause organs to increase in size?
A For dystrophy
B. With atrophy
B. With necrosis
D. With inflammation.
27.What changes cause cells to be destroyed?
A For necrosis
B. For dystrophy
B. With inflammation
G. With atrophy.
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