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socramed

Primary Sclerosing Cholangitis

~2 min readReviewed

In this topic9

  1. PSC Epidemiology and Course
  2. Forms of PSC
  3. PSC Pathogenesis
  4. PSC Clinical Features
  5. Cholangiography in PSC
  6. PSC Histology and Staging
  7. Diagnosing PSC
  8. PSC Complications
  9. PSC Management

Sclerosing cholangitis is a spectrum of cholestatic disorders — diseases in which the flow of bile is impaired — characterised by patchy inflammation, fibrosis and destruction of the intrahepatic and extrahepatic biliary tract. They are chronic and progressive, leading to biliary obstruction, cirrhosis, hepatic failure and the complications that follow. Secondary sclerosing cholangitis looks the same but is caused by a known disease or injury; when no such cause is found, the disease is called primary sclerosing cholangitis (PSC). The bile ducts narrow in multiple places at once, and it is this multifocal narrowing, not a single blockage, that the diagnosis is built on.

Choose a route through this family

If you are new to the topic, start with how common PSC is, who it affects and how it behaves over time, then how it is classified and why it develops.

Recognition follows: how PSC presents, what the bile ducts look like on imaging, and what a biopsy shows.

The last three carry the diagnosis through to what the disease means for the patient.

Read onward in this order if you are new to the topic: each note builds on the one before it.