Cirrhosis is a process of destruction of normal liver tissue, leaving scar tissue that is no longer able to perform its previous function, and the surrounding areas of liver tissue that still functions.
Most of the major causes of liver cirrhosis ends. In the U.S. the most common cause of cirrhosis of the misuse of alcohol. Among people aged 45-65 years, cirrhosis is the third leading cause of death after heart disease and cancer.In many parts of Asia and Africa, a major cause of cirrhosis is chronic hepatitis.
Causes of cirrhosis
• misuse of alcohol
• Taking certain medications
• Exposure to some chemicals
• Infection (including hepatitis B and hepatitis C)
• Autoimmune diseases (including autoimmune chronic hepatitis)
• blockage of the bile times (bile duct)
• Permanent fault flow of blood from the liver (as in Budd-Chiari syndrome)
• disturbance of the heart and blood vessels
• Lack of alpha-antitrypsin
• High levels of galactose in the blood
• High levels of tyrosine at birth (congenital tirosinosis)
• glycogen storage disease
• Diabetes mellitus (diabetes)
• Poor nutritional status (malnutrition)
• Inheritance accumulation of excessive amounts of copper, Wilson's disease)
• iron overload (hemochromatosis)
Symptoms
Many people with mild cirrhosis have no symptoms and appear healthy for years. Others are weak, have poor appetite, feel sick and lose weight. If bile flow is constantly clogged, a person has jaundice, itching, and small yellow skin nodules, especially around the eyelids. Poor nutritional status is usually the result of poor appetite and impaired absorption of fats and fat soluble vitamins (liposoluble vitamins) which is caused by a reduced formation of bile salts.
The person may cough or vomit a large amount of blood due to bleeding from varicose veins in the lower esophagus (esophageal varices). These enlarged blood vessels caused by high blood pressure in the veins that go from the gut to the liver. Such high blood pressure, called portal hypertension, with poor liver function may also lead to accumulation of free fluid in the abdomen (ascites). May occur and renal failure and hepatic encephalopathy.
May develop other symptoms of liver disease as long as the deterioration of muscle, red palms (palmar erythema), the curvature of the fingers (Dupuytren's contracture palmar), small veins in the skin like a spider, breast enlargement in men (gynecomastia), increased salivary glands in the cheeks , hair loss, dwarfing the testicles (testicular atrophy), and abnormal function of nerves (peripheral neuropathy).
Diagnosis
UZ can be shown that the liver is increased. Radioactive isotope liver scan creates an image that shows which areas of the liver are functioning and that the scar changed. Liver function test results are often normal, because the performance of basic chemical functions require only a small percentage of liver cells to function. The final diagnosis is microscopic examination of liver tissue samples.
Prognosis and treatment
Cirrhosis is usually progressive. If someone with early cirrhosis stops drinking, the process of changes of the liver scars are usually stopped, but scar tissue remains forever. Generally, the prognosis is worse if there were serious complications such as vomiting blood, ascites, abnormal brain function (encephalopathy).
Liver cancer (hepatocellular carcinoma) is more common in people with cirrhosis, which is a consequence of chronic infection with hepatitis B or hepatitis C, due to iron overload (hemochromatosis) due to long-term illness and storage (storage), and glycogen. In people with cirrhosis due to alcohol abuse can occur and liver cancer.
Cirrhosis can not be cured. However, the state seeks to improve elimination of toxic factors such as drinking alcohol, taking proper nutrition including vitamin and treatment of complications that occur.
A person with advanced cirrhosis of the liver transplant can help. But if a person continues to abuse alcohol or if you can not remove the causative agent of cirrhosis will eventually develop in the transplanted liver.
Primary biliary cirrhosis
• Introduction • Symptoms • Diagnosis and Treatment and Prognosis
Introduction
Primary biliary cirrhosis is an inflammation of the final scar changes and blockage of bile ducts in the liver.
Primary biliary cirrhosis is most common among women aged 35-60 years, although it can occur in men and women of any age. The cause is unknown, but the disease often occurs in people with autoimmune diseases such as rheumatoid arthritis, scleroderma, or autoimmune thyroiditis.
Primary biliary cirrhosis begins with inflammation of the bile ducts in the liver. Inflammation prevents the flow of bile from the liver so bile remains in the liver cells, or overflows into the bloodstream. Spread of infection to the rest of the liver, all the liver develops scar tissue trellis.
Symptoms and diagnosis
Primary biliary cirrhosis usually begin gradually. Itching and fatigue sometimes are the first symptoms in 50% of people with primary biliary cirrhosis, and these symptoms may precede other symptoms for months or years. At physical examination the doctor may feel for the people increased 50%, solid liver in about 25% increased spleen.About 15% have a small yellow deposits in the skin (xanthoma) or eyelids (xantelasma). About 10% have increased skin pigmentation. Less than 10% have only jaundice. Other symptoms may include an increase over the toes (toes batićasti) and abnormalities of the bones, nerves and kidneys. The diarrhea may be pale and fat and have a disgusting smell. Later you could have all the symptoms and complications of cirrhosis.
Diagnosis is at least 30% of people placed before the development of symptoms based on abnormalities detected during routine blood browsing. Antibodies against mitochondria (tiny structures within the cells) are found in the blood of more than 90% of people with the disease.
When jaundice and liver abnormalities Search apparent, effective diagnostic tool for the endoscopic retrograde cholangiopancreatography (ERCP). In the process, after the injection of radiocontrast material endoscopy in bile ducts, make the roentgenogram. It will show that within the bile duct is unobstructed and allow doctors to better establish the liver as the site of the problem. Diagnosis can be confirmed by microscopic examination of liver tissue samples obtained hollow needle (liver biopsy).
Treatment and Prognosis
Progression of primary biliary cirrhosis is very different. Initially, the disease does not reduce the quality of life of people with this disorder has a moderately good prognosis. It seems that the longer people live with the slow deterioration of the disease. For some the disease progresses relentlessly for several years, culminating in severe cirrhosis. The prognosis is poor in people with increased levels of bilirubin in the blood (jaundice). In most develop metabolic bone disease (osteoporosis).
Healing is not known. Itching can be combated by taking the medicine cholestyramine. May require supplements of calcium and vitamins A, D and K, because a lack of bile nutrients you absorb not satisfactory. The drug ursodiol (urso-deoksicholic acid) appears to be somewhat slow disease progression and is generally well tolerated.
The best treatment for those who enter the final stages of the complications of a liver transplant. Forecast for liver transplant is very good, it is less clear whether the transplanted primary biliary cirrhosis of the liver re-appear.
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