18. Mucoviscidosis pancreatis. Cystic Fibrosis / cystic fibrosis / a hereditary disorder of epithelial transport of chloride ions in mucus secretion in exocrine glands and the lining of the respiratory, gastrointestinal tract and pancreas In this case, the process affects pancreatic ductal cells from which the component produced exceptionally phlegm, blocked outgoing channels of the gland. They are expanding due to fluid retention with subsequent formation of retention cysts. The process is coupled with glandular atrophy and fibrosis around the canals. The preparation is described seeing changes - mostly dilated ducts filled with mucus retention periduktalnata fibrosis and cysts containing mucus pink homogeneous material.
Blog Archive
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2013
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28
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- October ( 4 )
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September
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21
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- 5. Necrosis cerebri /=№ 36. Infarctus anaemicus ce...
- 6. Emphysema pulmonis.
- 7. Atrophia fusca hepatis.
- 8. Cell swelling / Dystrophia parenchymatosa renis /
- 9.Corpus albicans ovarii.
- № 10. Fibrinoidna necrosis (bottom of a stomach ul...
- 11. Hyalinosis arteriolarum renis
- 12. Amyloidosis renis (HE).
- 13. Amyloidosis renis (MV).
- 14. Amyloidosis lienis (HE).
- 15. Amyloidosis lienis (MV).
- 16.Carcinoma gelatinosum (HE).
- 17.Carcinoma gelatinosum (alcian blau ).
- 18. Mucoviscidosis pancreatis.
- 19. Nаevus pigmentosus.
- 20. Induratio fusca pulmonis (HE)
- 21.Induratio fusca pulmonis (Histochemical reactio...
- 22.Icterus renis.
- 23.Anthracosis pulmonis
- 24. Steatosis hepatis = Dystrophia adiposa hepatis...
- 25. Dystrophia adiposa hepatis (Sudan III ).
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