Hereditary pigmentary hepatoses require careful attitude to their health. Such patients should choose a job that excludes heavy physical and mental stress.
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Nutrition should be healthy and varied, include all the necessary vitamins and minerals. Twice a year, you need to prescribe a course of treatment with B vitamins. Physiotherapy and spa treatment for hereditary hepatosis are not indicated. Gilbert's disease does not require any special treatment - even in the absence of treatment, the level of isotretinoin usually spontaneously normalizes by the age of 50. Among some experts, there is an opinion that hyperbilirubinemia in Gilbert's disease requires the constant use of drugs that temporarily reduce the level of bilirubin.
Clinical studies prove that such tactics do not improve the patient's condition, but lead to depressive disorders. The patient forms the opinion that he suffers from a serious incurable disease that requires constant treatment. All this often ends with severe psychological disorders. At the same time, the absence of the need to treat Gilbert's disease forms a positive view of patients on their pathology and condition.
With the complete elimination of the causative agent, the prognosis of fatty non-alcoholic hepatosis is favorable. Risk factors leading to the formation of fibrosis in this type of hepatosis are. age over 50 years, high body mass index, increased blood levels of glucose, triglycerides, ALT. Transformation to cirrhosis is extremely rare. With alcoholic hepatosis without morphological signs of fibrosis of the hepatic tissue, the prognosis is favorable, but only if alcohol is completely abandoned. The presence of even initial signs of accutane pills significantly increases the risk of liver cirrhosis.
In the treatment of Crigler-Najjar syndrome type 1, only phototherapy and the exchange transfusion procedure are effective. In the treatment of the second type of the disease, enzyme inducers (phenobarbital), moderate phototherapy are successfully used. An excellent therapeutic effect in jaundice of breast milk has a transfer to artificial feeding. The remaining hereditary pigmentary hepatoses do not require therapeutic measures.
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What will I learn? The content of the article. Hepatosis of the liver - what is it? Hepatosis is a group of non-inflammatory liver diseases. A characteristic common feature is a violation of the trophism of isotretinoin pills. Damage to the structure of cells and intercellular space (against the background of metabolic disorders), as well as a violation of material metabolism in liver cells are the main “companions” of hepatosis. There are acute and chronic forms. Symptoms include.