Primary Sclerosing Cholangitis (PSC) is a chronic condition of the liver whereby bile ducts within and without the liver are inflamed, scarred and constricted. Blocking the free flow of bile with time results in a progressive liver damage, cirrhosis and problems like bile duct infection or liver failure. PSC is notably related to inflammatory bowel disease especially ulcerative colitis although it may be independent.
PSC may progress slowly, and early on you might not notice any signs. As the disease advances, watch for:
The exact cause of PSC is not fully understood, but several factors appear to play a role:
It is our Jersey Village team of primary sclerosing cholangitis care-company that will cater to your needs in care provision; our professionals provide diagnostics, custom-made treatment regimens, and follow-up all under a single roof. Since the high-tech imaging (MRCP/ERCP) to the medical treatment and transplant coordination, we will be willing to maintain your liver functioning and to enhance your life quality.
Wait no longer to protect your liver. Book your appointment with our board certified Gastroenterologist of GastroDoxs in Jersey Village today, and receive the attentive, caring treatment that you are entitled to.
We've successfully treated more than 286 patients, helping individuals improve their digestive health and overall well-being through expert, personalized care.
With over 20 years of experience, GastroDoxs has been a trusted provider of gastroenterology care, focusing on delivering the best outcomes for patients
Both PSC and PBC are chronic bile duct liver diseases. PSC leads to inflammation and scarring of large and small ducts and occurs more frequently in men, whereas PBC mainly attacks small intrahepatic ducts.
Yes. Ulcerative colitis is also linked with PSC and is prevalent in nearly 70 percent of the patients, so the conditions have to be screened and monitored.
PSC does not come directly from your genes, but some genetic elements like HLA-B27 may predispose you. An autoimmune family history could also be a contributing factor.
PSC is characterized by abnormal liver function tests, serologic studies, and imaging examinations, such as MRCP or ERCP, which help detect constriction and scarring of the bile ducts.
Radiologic tests (MRCP or ERCP) show strictures, beading, and dilatation of bile ducts, which are used to confirm PSC and monitor the disease process.
Treatment involves ursodeoxycholic acid to enhance bile flow, endoscopic dilation (ERCP) of strictures, immunosuppressive or anti-inflammatory medications, and liver transplant in advanced stages.
Yes. By refraining from alcohol, maintaining a balanced diet, engaging in regular physical activities, and having prescribed vaccinations, liver health and wellness can be maintained.
Follow-up typically occurs every 6-12 months, but more frequent visits might be required in cases of symptom progression or complications.
PSC progresses slowly. Early diagnosis and proper treatment can maintain liver function, improve quality of life, and delay complications.
In Jersey Village, GastroDoxs has qualified gastroenterologists specializing in PSC. You can make a reservation for comprehensive examination, testing, and individualized care.