Primary Sclerosing Cholangitis
Primary Sclerosing Cholangitis (PSC) is a long-term disorder that affects the bile ducts in the liver. It is characterized by inflammation and scarring of the bile ducts which leads to gradual blockage of the flow of bile from the liver to the small intestine. This can lead to a variety of symptoms, including jaundice, fatigue, abdominal pain, and itching. In some cases, serious complications can occur if left untreated, such as liver failure, cirrhosis, or even primary biliary cholangitis. Treatment of PSC usually involves managing the symptoms and slowing down the progression of the disease. Medications, such as Ursodeoxycholic acid (UDCA) or corticosteroids, are used to reduce inflammation and reduce the size of the scarring. Surgery may also be recommended if the obstruction is severe. Primary Sclerosing Cholangitis is a serious condition that can affect quality of life, but proper diagnosis and treatment can help to manage symptoms and improve prognosis.
← Journal of Spleen And Liver Research