Secondary sclerosing cholangitis leads to slow and often irreversible
destruction of the walls of both intra- and extrahepatic bile ducts. A
s for primary sclerosing cholangitis, clinical signs and laboratory fi
ndings reveal cholestasis. The diagnosis is confirmed by retrograde en
doscopic cholangiography which shows narrowed bile ducts and rarefied
ramifications of the intra-hepatic ductal system. Several causes have
been identified including infectious causes with or without a relation
ship to bile duct obstruction and human immunodeficiency virus infecti
on as well as ischaemic related causes after chemotherapy, arterial em
bolization or Liver transplantation. Other causes include chemical agr
ession after treatment for hydatic cysts and post-surgical complicatio
ns due to a damaged bile tract. Treatment is difficult and often depen
dent on the cause.