Primary Sclerosing Cholangitis


What is primary sclerosing cholangitis?
Primary sclerosing cholangitis is a liver disease in which the bile ducts (small tubes through which bile flows from the liver to the gall bladder and intestines) progressively decrease in size due to inflammation and scarring. As a result, bile that is normally carried out of the liver accumulates within the liver, which then damages liver cells.

PSC illustration used with permission from MayoClinic.com. All rights reserved

How common is primary sclerosing cholangitis?
Although primary sclerosing cholangitis has been considered a rare disease, recent studies suggest that it is more common than originally thought. The disease may occur alone, but frequently exists in association with inflammatory diseases of the colon, such as chronic ulcerative colitis. Primary sclerosing cholangitis affects both sexes, but is more common in men.
What causes primary sclerosing cholangitis?
At the present time, the exact cause is unknown. However, there is currently no evidence that the disease is inherited, although some people may be more at risk because of inheriting a certain blood type. Viruses known to cause hepatitis have not been associated with primary sclerosing cholangitis. In many cases, this disease occurs in association with inflammatory bowel disease. This suggests that a common cause for both diseases may exist.
What are the symptoms of primary sclerosing cholangitis?

he course of primary sclerosing cholangitis is unpredictable and not well understood. A person can have the disease for many years before symptoms develop. They may include:

  • itching
  • fatigue
  • jaundice (yellowing of the skin and eyes)
  • episodes of fever and chills

If a person who suffers from primary sclerosing cholangitis develops fever and chills, he/she should go to the hospital immediately.  

 

How is primary sclerosing cholangitis diagnosed?

Since individuals may have no symptoms whatsoever for many years, the disease is often diagnosed because of abnormal liver blood tests.

How is primary sclerosing cholangitis treated?
Presently, there is no known specific treatment for primary sclerosing cholangitis. However, symptoms of this disease can be treated with varying success by antibiotics, vitamins and medications to control itching, improve bile flow, etc. Sometimes, insertion of a stent with a procedure known as endoscopy may be effective in alleviating jaundice and other symptoms. When the disease has progressed to liver failure, liver transplantation may be considered. Liver transplantation is successful in 80 to 90 percent of adult patients.

For more information on primary sclerosing cholangitis or any other liver diseases, please contact us.
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