Liver Dystrophy Glycogenous

Dystrophic changes in the liver can have a different nature. In the liver, dystrophic processes, like degenerative ones, are often combined with necrosis and atrophy. In dystrophic processes, the tissue is replaced by dense fibrous tissue. If the dystrophic process in some part of the gland does not tend to progress, dystrophy is called reversible in most cases. If the dystrophic or degenerative process becomes progressive, cirrhosis occurs; it is most often irreversible.

For most chronic liver diseases, the leading process during progression is the replacement of parenchyma (from the Latin parenchyma - tissue), containing a functionally active mass of cells, with connective tissue. Conventionally, this process can be defined as fibrosis. With the progression of chronic liver dystrophy with an increase in the thickness of the fibrous

Gliotic liver dystrophy is a severe and serious disorder of the liver, manifested as a result of disturbances in its functional activity. One of the most serious lesions is primary or secondary liver dysfunction of the glycogenic type. In this situation, we are talking about one of the most severe types of liver disorders. Pathological changes are accompanied by the accumulation of pathological glycogen inside hepatocytes.

Dystrophy of the gliosis type is an insidious and little-studied pathological condition, expressed in the death of a significant number of hepatocyte elements, as well as a disruption in the production of protective biochemical factors by the liver. The liver performs the function of a central filter: it receives