The Japanese Journal of Gastroenterological Surgery
Online ISSN : 1348-9372
Print ISSN : 0386-9768
ISSN-L : 0386-9768
CASE REPORT
A Case of Intrahepatic Peripheral Secondary Screrosing Cholangitis Diagnosed as Liver Malignant Tumor
Yuka MineRyuichiro SutoMasaaki HidakaKensuke MiyazakiToshiaki KameiNobuya Zempo
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2014 Volume 47 Issue 8 Pages 439-445

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Abstract
A 71-year-old man underwent pancreaticoduodenectomy (II region) for a pancreatic neuroendocrine tumor (PNET). He was periodically followed-up at an outpatient clinic. Six years after surgery, contrast-enhanced abdominal CT revealed a tumorous lesion, measuring 20 mm, with an unclear border and enhancement effects on the S4 liver surface. MRI with gadolinium ethoxybenzyl diethylenetriaminepentaacetic acid (Gd-EOB-DTPA-enhanced MRI) also showed a low-signal-intensity area at the same site in the hepatocellular phase. Under a tentative diagnosis of primary liver cancer or metastatic liver tumor from PNET, partial hepatectomy (S4) was conducted. In the resected specimen, a white, irregular mass with a clear border was observed. Histopathological findings included marked fibrous thickening of the bile duct wall and the infiltration of inflammatory cells, leading to a diagnosis of sclerosing cholangitis. His medical history suggested secondary sclerosing cholangitis after biliary-tract reconstruction. To the best of our knowledge, there have been no case reports published on secondary sclerosing cholangitis localized in the peripheral intrahepatic bile duct. Although a preoperative diagnosis is difficult, resection should be considered if the possibility of malignant tumors cannot be ruled out.
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この記事はクリエイティブ・コモンズ [表示 - 非営利 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc/4.0/deed.ja
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