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胆管内乳头状肿瘤,从肝内胆管向肝外胆管浅表性延伸。

Intraductal papillary neoplasm of the bile duct extending superficially from the intrahepatic to extrahepatic bile duct.

作者信息

Nanashima Atsushi, Sumida Yorihisa, Tamaru Naoe, Nakanuma Yasuni, Abo Takafumi, Tanaka Kenji, Sawai Terumitsu, Yasutake Toru, Nagayasu Takeshi, Hayashi Tomayoshi, Fukuda Yasuhiro

机构信息

Division of Surgical Oncology, Department of Translational Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences, Japan.

出版信息

J Gastroenterol. 2006 May;41(5):495-9. doi: 10.1007/s00535-006-1803-4.

Abstract

Intraductal papillary neoplasm of the bile duct (IPNB) or liver is a recently noted rare disease, and its pathogenesis remains unclear. Here we present a case of IPNB with an interesting morphology, which was treated by resection of the right hemiliver and extrahepatic bile duct. A 79-year-old woman was found to have a high alkaline phosphatase level and slight dilatation of the right intrahepatic bile duct on imaging studies. The right intrahepatic bile duct became dilated over a 2-year period; however, no solid mass could be detected, and tumor markers were not elevated. Hepatic resection was scheduled because a mucin-producing bile duct carcinoma of the liver was suspected. A right hemihepatectomy was conducted, and the extrahepatic bile duct was also resected after malignant cells were found in the surgical stump of the right bile duct and in the bile itself. Macroscopically, diffuse dilatation of the intrahepatic bile duct was noted, but no solid component or mucin within the duct was found. Histopathological findings revealed carcinoma in situ, IPNB, in the majority of intrahepatic bile ducts, with no lymph node metastasis, and it extended continuously to the epithelium of the common bile duct. No tumor recurrence or biliary dilatation was observed at follow-up 2 years after surgery. It is important to consider malignancy in the presence of a dilated bile duct and in the absence of any cause of occlusion. Complete resection of IPNB results in a good prognosis and no recurrence.

摘要

胆管或肝脏的导管内乳头状肿瘤(IPNB)是一种最近才被发现的罕见疾病,其发病机制尚不清楚。在此,我们报告一例具有有趣形态学表现的IPNB病例,该病例通过右半肝和肝外胆管切除术进行治疗。一名79岁女性在影像学检查中发现碱性磷酸酶水平升高,右肝内胆管轻度扩张。右肝内胆管在2年时间里逐渐扩张;然而,未检测到实性肿块,肿瘤标志物也未升高。由于怀疑为肝脏黏液分泌性胆管癌,计划进行肝切除术。实施了右半肝切除术,并且在右胆管手术切端和胆汁中发现恶性细胞后,也切除了肝外胆管。肉眼可见肝内胆管弥漫性扩张,但未在胆管内发现实性成分或黏液。组织病理学检查结果显示,大多数肝内胆管存在原位癌,即IPNB,无淋巴结转移,且连续延伸至胆总管上皮。术后2年随访未观察到肿瘤复发或胆管扩张。在存在胆管扩张且无任何梗阻原因的情况下,考虑恶性病变很重要。IPNB的完整切除可带来良好预后且无复发。

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