We reported two cases of localized primary sclerosing cholangitis (PSC) mimicking bile duct cancer in our department.
Case 1: a 72-years-old woman was admitted to the hospital, because she was pointed out elevations of serum enzymes(ALP, γ-GTP). Ultrasonography and abdominal CE-CT scan revealed dilatation of the left hepatic bile duct. Endoscopic retrograde cholangiography (ERC)revealed the obstructed left hepatic bile duct. We suspected bile duct cancer and performed left hepatic lobectomy. Pathological examination of the resected specimen revealed sclerosing cholangitis.
Case 2: a 78-years-old woman was admitted with a chief complaint of epigastric pain. Gastrofiberscope revealed gastric ulcer (active stage) in the gastric angle. Ultrasonography revealed a cystic lesion in the left hepatic lobe. Percutaneous transhepatic cholangiography (PTC) revealed a narrowed lesion 1 cm in length which was localized in the left intrahepatic bile duct (IHBD). We suspected cholangiocellular carcinoma and perfomed left hepatic lobectomy. Pathological examination of the resected specimen revealed sclerosing cholangitis
According to the standard criterion, final diagnosis of primary sclerosing cholangitis was made in both cases. It is considered that localized PSC is difficult to diagnose and surgical resection is recommended because of high possibility of the progression of the lesion and the combinations with cholangiocellular carcinoma.
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