Primary sclerosing cholangitis

Primary sclerosing cholangitis (PSC) is an uncommon inflammatory condition, which affects the biliary tree resulting in multiple strictures, liver damage, and eventually cirrhosis.

The diagnosis can be made when there are classical imaging features in the correct clinical context, and secondary causes of cholangitis have been excluded 16

PSC is strongly associated with inflammatory bowel disease (IBD) (in 70% cases 6), especially ulcerative colitis, and thus shares similar demographics: young to middle-aged males (~4th decade) are most frequently affected 4 .

The average age of diagnosis is 54 years (range 6-93) with increased occurrence in men (63%) 15. A large number of asymptomatic individuals are identified upon investigation of persistently deranged liver function tests. Symptomatic individuals commonly present non-specifically with fatigue. More specific symptoms include pruritus, jaundice or GI bleeding 16.

Unfortunately, no histological findings are pathognomonic for PSC 2. Frequent findings include 2-4:

  • periductal fibrosis (onion skin lesions)
  • periportal eosinophilic infiltrate
  • paucity of ducts

Unlike primary biliary cirrhosis, antibody titers are usually absent or low 4. Liver function tests will usually have a cholestatic pattern with elevated alkaline phosphatase (ALP) and bilirubin 2.

The entire biliary tree (both intra and extrahepatic) may be involved, with multiple strictures scattered along its length. In ~20% only the intrahepatic and proximal extrahepatic bile ducts are involved4.

The end result of PSC is cirrhosis which is usually characterized by a markedly distorted biliary tract with atrophy of the entire liver with the exception of the caudate lobe which is hypertrophied in almost all cases (68-98%) 1-5. Atrophy involving the left lobe is a feature which somewhat distinguishes it from cirrhosis from other causes, in which the left lobe is usually hypertrophied 1.

Ultrasound is able to demonstrate both the changes of cirrhosis and irregularity of bile duct caliber. Additionally, brightly echogenic portal triads may be visible.

Gallbladder polyps should be considered malignancy until proven otherwise.

  • contour abnormalities and atrophy (see above)
  • marked caudate lobe hypertrophy
  • the atrophied liver is of lower density than the hypertrophied caudate lobe 1
  • multiple linear discontinuous low-density regions representing dilated intrahepatic bile duct segments 1

ERCP has traditionally been the gold standard for the depiction of the biliary tree, and also offers the ability to perform cholangioplasty, if necessary. In practice, however, MRCP is used before ERCP since it is noninvasive, can visualize the liver, and it avoids the 10% risk of hospitalization from ERCP in PSC patients 17.

The characteristic findings on direct imaging of the biliary tree are 2,3,5:

  • multiple segmental strictures
    • typically short segment
    • intervening segments are of normal caliber or slightly dilated (beading)
  • biliary dilatation: may be present in ~85% of cases 9
    • general: ~35%
    • segmental: ~50%
  • biliary diverticula
  • mural irregularities
  • distortion of the biliary tree due to associated cirrhosis

The only cure available at present is orthotopic liver transplantation (OLT) with 5-year survival rates approaching 80% 10,11. However, there is evidence that PSC may recur in 5-20% of patients post-transplantation 10-12.

No medical therapy has stood the test of time, with ursodeoxycholic acid, immunosuppression, chelation and antifibrolytic therapy unable to demonstrate consistent benefits over placebo 8.

Percutaneous cholangioplasty of dominant strictures is usually performed in a retrograde fashion via ERCP or via a transhepatic approach 6,7.

General imaging differential considerations include:

Gallbladder and biliary tract pathology
Hepatobiliary pathology

Article information

rID: 7007
Synonyms or Alternate Spellings:
  • Primary sclerosing cholangitis (PSC)

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Cases and figures

  • Primary sclerosin...
    Case 1
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  • Case 2
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  • Case 3: with concurrent pancreatitis
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  • Case 3
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  • Case 4
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  • Case 5
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  • Case 6: non-contrast CT
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  • Case 6: MRI gradient echo
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  • Case 7: coronal thick slab HASTE
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  • Case 8
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