학술논문

Primary sclerosing cholangitis complicated with cholangiocarcinoma / 原発性硬化性胆管炎に合併した胆管癌
Document Type
Journal Article
Source
胆道 / Tando. 2015, 29(4):732
Subject
cholangiocarcinoma
imaging diagnosis
primary sclerosing cholangitis
原発性硬化性胆管炎
画像診断
胆管癌
Language
Japanese
ISSN
0914-0077
1883-6879
Abstract
Background: Primary sclerosing cholangitis (PSC) complicated with cholangiocarcinoma (CC) is rarely reported in Japan. Methods: In this study, we investigated 38 patients with PSC retrospectively. A total of 5 patients (13.2%) had CC. This rate corresponds to that reported in Western countries. Results: The mean age at CC diagnosis was 49.6 years (range: 31-65 years), and 2 patients were women. Three of 5 patients did not suffer from cirrhosis. No significant difference was observed in background characteristics between patients with and without CC. Three of 5 patients were diagnosed with CC at the same time or within the first year after diagnosis of PSC. CC manifested as bile duct stricture or mass formation. Two of 5 patients exhibited mass formation in this study. The prognosis of patients with CC was poor, and all patients died. The median survival time was 1.04 years (range: 0.2-3.3 years). Conclusions: Patients with PSC should be carefully monitored for CC development using an imaging modality, particularly within the first year after diagnosis of PSC.

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