An atypical case of isolated immunoglobulin G4-related sclerosing cholangitis with a cholangiogram resembling primary sclerosing cholangitis

Clin J Gastroenterol. 2024 Apr;17(2):338-344. doi: 10.1007/s12328-023-01903-w. Epub 2024 Jan 3.

Abstract

An asymptomatic 77-year-old man with intrahepatic bile duct dilation was referred to our hospital. Cholangiography revealed alternations between strictures and dilated segments from the right and left hepatic ducts to the lower bile ducts, with findings of a pruned tree, beaded, shaggy appearance, and diverticulum-like outpouching. Histopathology revealed abundant immunoglobulin G4 (IgG4)-positive plasma cells (> 10 per high-power field) with an IgG4/IgG-positive cell ratio of 40-50%. After 2 weeks of steroid therapy, the cholangiography markedly improved. Because the cholangiographic findings resembled those of primary sclerosing cholangitis, steroid therapy proved useful in differentiating IgG4-related sclerosing cholangitis from primary sclerosing cholangitis.

Keywords: Endoscopic retrograde cholangiography; Intraductal ultrasonography; Isolated IgG4-related sclerosing cholangitis; Primary sclerosing cholangitis; Steroid therapy.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Bile Ducts / diagnostic imaging
  • Bile Ducts / pathology
  • Cholangiography
  • Cholangitis, Sclerosing* / diagnostic imaging
  • Cholangitis, Sclerosing* / drug therapy
  • Diagnosis, Differential
  • Humans
  • Immunoglobulin G
  • Male
  • Steroids

Substances

  • Immunoglobulin G
  • Steroids