If the ducts that lead from the liver to the duodenum sustain enough damage, or experience repeated bouts of cholangitis, gallstones, or other conditions that affect this tissue, the defense mechanism of the body is to develop scar tissue, which can then hinder the movement of bile secretions. Increased scarring leads to more damage, and forces bile back into the liver, which damages liver cells.
While many conditions are implicated in the development of PSC, no root cause has yet been determined. It is thought that genetics may play a role in PSC, as well as possibly viruses and bacteria. Additionally, it has been noted that many patients with PSC also have immune problems and/or suffer from ulcerative colitis.
Primary sclerosing cholangitis develops over time, as repeated attacks of gallstones and cholangitis cause the hardening of the duct walls. Although it can affect people of all ages, it primarily affects men over the age of forty.
Symptoms may include:
Blood tests to check levels of liver enzymes are the first step in diagnosing primary sclerosing cholangitis. Doctors confirm the diagnosis using cholangiography, which provides pictures of the bile ducts.
Cholangiography can be performed in the following ways:
Other testing may include ultrasound exams and a liver biopsy. Ultrasound uses sound waves to create images of organs inside the body. A biopsy involves removal of a small piece of tissue for examination with a microscope.
Although researchers have studied many treatments, none has been shown to cure or slow the progress of primary sclerosing cholangitis. Treatment of PSC aims to relieve symptoms and manage complications. Medical treatment may include various medications to relieve itching, antibiotics to treat infections, and vitamin supplements. Instruments passed through an endoscope during ERCP can help open blocked bile ducts. Liver transplantation may be an option if the liver begins to fail.
Primary sclerosing cholangitis can lead to various complications, including: