Hilar cholangiocarcinoma with extensive immunoglobulin G4 reaction

• Published in: International journal of clinical and experimental pathology Vol. 14; no. 9; pp. 987 - 992
• Main Authors: Yamamura, Minako, Sato, Yasunori, Takahashi, Kenta, Nguyen Canh, Hiep, Li, Zihan, Kimoto, Tatsuya, Terasaki, Shuichi, Harada, Kenichi
• Format: Journal Article
• Language: English
• Published: e-Century Publishing Corporation 15-09-2021
• Subjects: Case Report
• ISSN: 1936-2625

Immunoglobulin G4 (IgG4)-related disease (IgG4-RD) is a systemic fibroinflammatory disorder that can involve multiple organs. It is often challenging to distinguish IgG4-related sclerosing cholangitis (IgG4-SC) from cholangiocarcinoma because of overlap in their clinical findings. A 75-year-old man presented to a hospital for a detailed examination of the elevation of some biliary enzymes. Radiographic examination revealed segmental bile duct with wall thickening of the common hepatic bile duct, and dilation of the peripheral branches. Transampullary biopsy showed a non-specific inflammatory reaction with several IgG4-positive cell infiltrations. There were no signs of malignancy. The liver biopsy showed bile duct injury accompanied by IgG4-positive cell infiltration. We then performed bile duct biopsy and finally diagnosed the patient with cholangiocarcinoma. We should remember that the IgG4 reaction is neither completely sensitive nor specific for IgG4-RD and avoid resting solely on the IgG4 reaction to precisely distinguish IgG4-SC from cholangiocarcinoma.