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DEGENERATIONS 
(dystrophy)
Degeneration (dystrophy) 
is a pathological process due to 
disturbance of either cellular or 
tissue metabolism which causes 
changes in the structure of cells, 
tissues, etc.
Trophism mechanisms are cellular and 
extracellular: 
cellular: autoregulation (enzymes) 
extracellular: transportation systems 
(blood, lymph); endocrine regulation;
Morphogenetic mechanisms of degenerations: 
 infiltration: abundant invasion of metabolite 
products from the transportation system to the cell 
followed by their accumulation; 
 decomposition: destruction of cellular 
ultrastructure (lipoprotein complex from cellular 
membranes) with accumulation within a cell; 
 abnormal synthesis: intracellular synthesis of the 
substances which are not produced normally (e.g. 
amyloid); 
 transformation: formation of products of one type 
of metabolism from the common primary products, 
e.g. increased polymerization of glycogen from 
glucose.
Classification of degenerations 
 According to the localization: 
a) parenchymatous (intracellular accumulation), 
b) mesenchymatous (extracellular accumulation), 
c) mixed type. 
 According to the type of metabolism disturbance: 
a) albuminous (protein), 
b) fatty (adipose), (lipidosis), 
c) carbohydrate, 
d) mineral 
 According to the origin: 
a) acquired, 
b) heriteted. 
 According to propagation 
a) general, 
b) local.
Parenchymatous degenerations 
Parenchymatous albuminous 
degenerations (dysproteinoses)
The modern classification of 
parenchymatous albuminous 
degenerations: 
1) hyalin-drop 
2) hydropic (edematous, balloon)
Hyalin-drop degeneration 
Microscopically: rounded, eosinophilic 
droplets, vacuoles, or aggregates in the 
cytoplasm 
Macroscopically: organs enlarged, 
flabby, grey colour on section 
Localizations: kidney, liver, 
myocardium
Hydropic degeneration 
 Microscopically: large vacuoles of cytoplasm 
fluid in the cytoplasm, the nucleus which 
displaced to the peripheral areas 
 Macroscopically: organs enlarged, flabby, 
grey colour on section 
 Localizations: kidneys, skin, liver, muscles, 
nerves
Horny degeneration 
abundant formation of horny substance 
in keratinized epithelium 
(hyperkeratosis and ichtyosis) 
appearance of horny substance in the 
places where is not found under normal 
conditions (leukoplakias)
Parenchymatous degenerations 
Parenchymatous fatty 
degenerations
Manifestation 
of disturbance of fat metabolism: 
appearance of fat in the place where it 
does not appear under normal 
conditions (e.g. in the myocardium), 
appearance of fat of unusual 
composition; 
increase of fat amount in the places 
where it is present under normal 
conditions (e.g. in the fat depots).
Hypoxia - the main cause of fatty 
degeneration 
disturbances in transportation systems 
(e.g. in patient with chronic 
cardiovascular and chronic pulmonary 
insufficiency); 
chronic intoxications (e.g. alcoholism); 
cachexia, avitaminosis; 
infections (e.g. diphtheria, tuberculosis).
Parenchymatous degenerations 
Parenchymatous carbohydrate 
degenerations
Glycogen metabolism disturbance 
increase or reduction in the amount in 
the tissues where it is present under 
normal conditions, 
its appearance in the areas where it is not 
present under normal conditions
Storage diseases 
(enzymopathy) 
proteinoses 
lipidosis 
glucogenoses
Thank you for your attention

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Intracellular accumulations

  • 2. Degeneration (dystrophy) is a pathological process due to disturbance of either cellular or tissue metabolism which causes changes in the structure of cells, tissues, etc.
  • 3. Trophism mechanisms are cellular and extracellular: cellular: autoregulation (enzymes) extracellular: transportation systems (blood, lymph); endocrine regulation;
  • 4. Morphogenetic mechanisms of degenerations:  infiltration: abundant invasion of metabolite products from the transportation system to the cell followed by their accumulation;  decomposition: destruction of cellular ultrastructure (lipoprotein complex from cellular membranes) with accumulation within a cell;  abnormal synthesis: intracellular synthesis of the substances which are not produced normally (e.g. amyloid);  transformation: formation of products of one type of metabolism from the common primary products, e.g. increased polymerization of glycogen from glucose.
  • 5. Classification of degenerations  According to the localization: a) parenchymatous (intracellular accumulation), b) mesenchymatous (extracellular accumulation), c) mixed type.  According to the type of metabolism disturbance: a) albuminous (protein), b) fatty (adipose), (lipidosis), c) carbohydrate, d) mineral  According to the origin: a) acquired, b) heriteted.  According to propagation a) general, b) local.
  • 6. Parenchymatous degenerations Parenchymatous albuminous degenerations (dysproteinoses)
  • 7. The modern classification of parenchymatous albuminous degenerations: 1) hyalin-drop 2) hydropic (edematous, balloon)
  • 8. Hyalin-drop degeneration Microscopically: rounded, eosinophilic droplets, vacuoles, or aggregates in the cytoplasm Macroscopically: organs enlarged, flabby, grey colour on section Localizations: kidney, liver, myocardium
  • 9.
  • 10. Hydropic degeneration  Microscopically: large vacuoles of cytoplasm fluid in the cytoplasm, the nucleus which displaced to the peripheral areas  Macroscopically: organs enlarged, flabby, grey colour on section  Localizations: kidneys, skin, liver, muscles, nerves
  • 11. Horny degeneration abundant formation of horny substance in keratinized epithelium (hyperkeratosis and ichtyosis) appearance of horny substance in the places where is not found under normal conditions (leukoplakias)
  • 12.
  • 14. Manifestation of disturbance of fat metabolism: appearance of fat in the place where it does not appear under normal conditions (e.g. in the myocardium), appearance of fat of unusual composition; increase of fat amount in the places where it is present under normal conditions (e.g. in the fat depots).
  • 15. Hypoxia - the main cause of fatty degeneration disturbances in transportation systems (e.g. in patient with chronic cardiovascular and chronic pulmonary insufficiency); chronic intoxications (e.g. alcoholism); cachexia, avitaminosis; infections (e.g. diphtheria, tuberculosis).
  • 16.
  • 17.
  • 18.
  • 19. Parenchymatous degenerations Parenchymatous carbohydrate degenerations
  • 20. Glycogen metabolism disturbance increase or reduction in the amount in the tissues where it is present under normal conditions, its appearance in the areas where it is not present under normal conditions
  • 21. Storage diseases (enzymopathy) proteinoses lipidosis glucogenoses
  • 22. Thank you for your attention