M. Sebagh et al., SCLEROSING CHOLANGITIS FOLLOWING HUMAN ORTHOTOPIC LIVER-TRANSPLANTATION, The American journal of surgical pathology, 19(1), 1995, pp. 81-90
Sclerosing cholangitis defined by cholangiographic criteria may occur
after orthotopic liver transplantation. In this retrospective study, w
e analyzed failed grafts and antecedent serial biopsies of 24 patients
who developed this type of nonanastomotic biliary strictures. Scleros
ing cholangitis was histologically diagnosed if there was a combinatio
n of periductal fibrosis and features of large bile duct obstruction.
The condition was observed in all but one available failed allografts.
This later showed ischemic-type lesions without periductal fibrosis.
Liver biopsy specimens were nondiagnostic relative to sclerosing chola
ngitis, although 85% of the patients had evidence of large bile duct o
bstruction. Numerous associated factors may explain the pathogenesis o
f secondary sclerosing cholangitis: an immunologically related etiolog
ic factor (10 recipients of ABO-incompatible allografts) and compromis
ed arterial blood flow that likely resulted from hepatic artery thromb
osis (12 patients), focal arterial fibrointimal hyperplasia (three pat
ients), chronic ductopenic arteriopathic rejection (three patients) an
d/or preservation-related ischemia (four patients). Sclerosing cholang
itis may be a significant cause of graft failure that often has mislea
ding biopsy manifestations. From a practical standpoint, cholestasis w
ith evidence of large bile duct obstruction warrants cholangiographic
assessment of the biliary tree.