Open Access Articles- Top Results for Primary sclerosing cholangitis

Primary sclerosing cholangitis

Primary sclerosing cholangitis
Cholangiogram of primary sclerosing cholangitis.
Classification and external resources
ICD-10 K83.0
ICD-9 576.1
OMIM 613806
DiseasesDB 10643
MedlinePlus 000285
eMedicine med/3556
NCI Primary sclerosing cholangitis
Patient UK Primary sclerosing cholangitis
MeSH D015209

Primary sclerosing cholangitis (PSC) is a disease of the bile ducts that causes inflammation and subsequent obstruction of bile ducts both inside and outside of the liver. The inflammation impedes the flow of bile to the gut, which can ultimately lead to cirrhosis of the liver, liver failure, and liver cancer. The underlying cause of the inflammation is believed to be autoimmunity;[1] and more than 80% of those with PSC have ulcerative colitis.[2] The definitive treatment is a liver transplant.

Signs and symptoms

PSC is characterized by recurrent episodes of cholangitis (inflammation of the bile ducts), with progressive biliary scarring and obstruction.


The cause of PSC is unknown, although it is thought to be an autoimmune disorder. There is an increased prevalence of HLA alleles A1, B8, and DR3 in primary sclerosing cholangitis.[1]


Inflammation leads to sclerosis or damage of bile ducts both inside and outside of the liver. The resulting scarring of the bile ducts blocks the flow of bile, causing cholestasis. Bile stasis and back-pressure induces proliferation of epithelial cells and focal destruction of the liver parenchyma, forming bile lakes. Chronic biliary obstruction causes portal tract fibrosis and ultimately biliary cirrhosis and liver failure.[3]
Bile assists in the intestinal breakdown and absorption of fat; the absence of bile leads to fat malabsorption and deficiencies of fat-soluble vitamins (A, D, E, K).[citation needed]


PSC is diagnosed by visualizing the bile duct with imaging, usually in the setting of endoscopic retrograde cholangiopancreatography (ERCP), which shows "beading" (both strictures and dilation) of bile ducts inside and outside of the liver. Another option is magnetic resonance cholangiopancreatography (MRCP), where magnetic resonance imaging is used to visualize the biliary tract.

Most people with PSC have evidence of autoantibodies. Approximately 80% of people with PSC have perinuclear anti-neutrophil cytoplasmic antibodies; however, this finding is not specific to those with the disease. Antinuclear antibodies and anti-smooth muscle antibody are found in 20%-50% of PSC patients and, likewise, are not specific for the disease.[1]

Other tests often done are a full blood count, liver enzymes, bilirubin levels (usually grossly elevated), kidney function, and electrolytes. Fecal fat determination is occasionally ordered when the symptoms of malabsorption are prominent.

The differential diagnosis can include primary biliary cirrhosis, drug induced cholestasis, cholangiocarcinoma, and HIV-associated cholangiopathy.


Standard treatment includes ursodiol, a bile acid naturally produced by the liver, which has been shown to lower elevated liver enzyme numbers in people with PSC, but has not improved liver- or overall survival.[4] Treatment also includes medication to relieve itching (antipruritics), bile acid sequestrants (cholestyramine), antibiotics to treat infections, and vitamin supplements, as people with PSC are often deficient in vitamin A, vitamin D, vitamin E, and vitamin K.

In some cases, ERCP, which may involve stenting of the common bile duct, may be necessary in order to open major blockages (dominant strictures).[citation needed]

Liver transplantation is the only proven long-term treatment of PSC. Indications for transplantation include recurrent bacterial cholangitis, jaundice refractory to medical and endoscopic treatment, decompensated cirrhosis and complications of portal hypertension. In one series, 1, 2, and 5 year survival following liver transplantation for PSC was 90%, 86% and 85% respectively.[1]


A German study in 2007 estimated the average survival time from time of diagnosis to be approximately 25 years, and the median time until either death or liver transplantation to be approximately 10 years.[5]

Related diseases

Primary sclerosing cholangitis is associated with cholangiocarcinoma,[6] a cancer of the biliary tree, and the lifetime risk for PSC sufferers is 10-15%.[7] This represents a 160-fold greater risk of developing cholangiocarcinoma compared to the general population.[7] Screening for cholangiocarcinoma in patients with primary sclerosing cholangitis is encouraged, but there is no general consensus on the modality and interval of choice.[citation needed] Colon cancer is also associated with PSC.[6]

PSC has a significant association with ulcerative colitis, an inflammatory bowel disease primarily affecting the large intestine. As many as 5% of patients with ulcerative colitis may progress to develop primary sclerosing cholangitis[8] and approximately 70% of people with primary sclerosing cholangitis have ulcerative colitis.[3]


There is a 2:1 male-to-female predilection of primary sclerosing cholangitis.[3] The disease normally starts from age 20 to 30, though may begin in childhood. PSC progresses slowly, so the disease can be active for a long time before it is noticed or diagnosed. There is relatively little data on the prevalence and incidence of primary sclerosing cholangitis, with studies in different countries showing annual incidence of 0.068–1.3 per 100,000 people and prevalence 0.22–8.5 per 100,000; given that PSC is closely linked with ulcerative colitis, it is likely that the risk is higher in populations where UC is more common.[9]

See also


  1. ^ a b c d Charatcharoenwitthaya P, Lindor KD (Feb 2006). "Primary sclerosing cholangitis: diagnosis and management". Current Gastroenterology Reports 8 (1): 75–82. PMID 16510038. doi:10.1007/s11894-006-0067-8. 
  2. ^ Sleisenger, MH (2006). Sleisenger and Fordtran's gastrointestinal and liver disease: pathophysiology, diagnosis, management (8th ed.). Philadelphia: Saunders. 
  3. ^ a b c Robbins SL, Kumar V, Cotran RS (2003). "Chapter 16". Robbins basic pathology (7th ed.). Philadelphia: Saunders. pp. 620–1. ISBN 0-7216-9274-5. 
  4. ^ Lindor KD, Kowdley KV, Luketic VA, Harrison ME, McCashland T, Befeler AS, Harnois D, Jorgensen R, Petz J, Keach J, Mooney J, Sargeant C, Braaten J, Bernard T, King D, Miceli E, Schmoll J, Hoskin T, Thapa P, Enders F (Sep 2009). "High-dose ursodeoxycholic acid for the treatment of primary sclerosing cholangitis". Hepatology 50 (3): 671–3. PMC 2758780. PMID 19585548. doi:10.1002/hep.23082. 
  5. ^ Tischendorf, J.; Hecker, H.; Krüger, M.; Manns, M.; Meier, P. (2007). "Characterization, outcome, and prognosis in 273 patients with primary sclerosing cholangitis: A single center study". The American journal of gastroenterology 102 (1): 107–114. PMID 17037993. doi:10.1111/j.1572-0241.2006.00872.x.  edit [1]. Giving survival time: 306 months
  6. ^ a b Tsaitas C, Semertzidou A, Sinakos E (April 2014). "Update on inflammatory bowel disease in patients with primary sclerosing cholangitis". World J Hepatol 6 (4): 178–87. PMC 4009473. PMID 24799986. doi:10.4254/wjh.v6.i4.178. 
  7. ^ a b Kummen M, Schrumpf E, Boberg KM (August 2013). "Liver abnormalities in bowel diseases". Best Pract Res Clin Gastroenterol 27 (4): 531–42. PMID 24090940. doi:10.1016/j.bpg.2013.06.013. 
  8. ^ Olsson R, Danielsson A, Järnerot G et al. (1991). "Prevalence of primary sclerosing cholangitis in patients with ulcerative colitis". Gastroenterology 100 (5 Pt 1): 1319–23. PMID 2013375. 
  9. ^ Feld JJ, Heathcote EJ (October 2003). "Epidemiology of autoimmune liver disease". J. Gastroenterol. Hepatol. 18 (10): 1118–28. PMID 12974897. doi:10.1046/j.1440-1746.2003.03165.x. 

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