217.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.
218. 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.
219.What changes cause organs to decrease in size?
A For atrophy
B. For dystrophy
B. With necrosis
D. With inflammation.
220.What changes cause organs to increase in size?
A For dystrophy
B. With atrophy
B. With necrosis
D. With inflammation.
221.What changes cause cells to be destroyed?
A For necrosis
B. For dystrophy
B. With inflammation
G. With atrophy.
222. Types of intracellular dysproteinoses?
A Hydropic, hyaline drops
B.Hyalinosis, amyloidosis
B.Mucoid, fibrinoid
G. Chromotoproteins, nucleoproteins.
223. Types of mixed dysproteinoses?
A Chromotoproteins, nucleoproteins
B. Amyloid, hyaline
B. Hydropic, granular-protein dystrophy
G. Hyalinosis, amyloidosis.
224.Theory explaining the pathogenesis of dystrophy?
A Decomposition, infiltration, transformation
B. Degenerative, infiltrative
B. Viral, polyetiological
G. Amyloid, hyaline.
A Hyalinosis, amyloidosis
B. Mucoid, phyrinoid
V.Hyaline drops
G. Hydropic dystrophy.
226. Specify the types of local atrophy?
A Angiogenic, neurogenic
B. General, local
B. Infiltrative, degenerative
G.Mucoid, phyrinoid.
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