In sarcoidosis, granulomas are frequently present in multiple organs,
including the liver. Typically, epithelioid granulomas (noncaseating)
are scattered throughout the liver, but confluent granulomas can be pr
esent in cases with severe hepatic involvement. The characteristic inc
lusions in giant cells (for example, Schaumann bodies and asteroid bod
ies) are not seen in all cases and are not pathognomonic, The granulom
as of sarcoidosis may heal without a trace, but confluent granulomas c
an result in extensive, irregular scarring. Occlusion of intrahepatic
portal vein branches by the granulomatous inflammation probably accoun
ts for the development of portal hypertension in some cases. A granulo
matous cholangitis leading to ductopenia seems to be the underlying pa
thogenetic mechanism of the chronic cholestatic syndrome of sarcoidosi
s. Recognition of this syndrome is important in the differential diagn
osis of other chronic cholestatic diseases, such as primary biliary ci
rrhosis or primary sclerosing cholangitis. Other rare complications of
sarcoidosis are the Budd-Chiari syndrome and obstructive jaundice att
ributable to hepatic hilar lymphadenopathy or strictures of the bile d
ucts.