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黏液高分泌性胆管肿瘤,其临床病理特征与胰腺导管内乳头状黏液性肿瘤(IPMN)相似。

Mucin-hypersecreting bile duct neoplasm characterized by clinicopathological resemblance to intraductal papillary mucinous neoplasm (IPMN) of the pancreas.

作者信息

Yamashita Yo-Ichi, Fukuzawa Kengo, Taketomi Akinobu, Aishima Shinichi, Yoshizumi Tomoharu, Uchiyama Hideaki, Tsujita Eiji, Harimoto Norifumi, Harada Noboru, Wakasugi Kenzo, Maehara Yoshihiko

机构信息

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

World J Surg Oncol. 2007 Aug 28;5:98. doi: 10.1186/1477-7819-5-98.

Abstract

BACKGROUND

Although intraductal papillary mucinous neoplasm (IPMN) of the pancreas is acceptable as a distinct disease entity, the concept of mucin-secreting biliary tumors has not been fully established.

CASE PRESENTATION

We describe herein a case of mucin secreting biliary neoplasm. Imaging revealed a cystic lesion 2 cm in diameter at the left lateral segment of the liver. Duodenal endoscopy revealed mucin secretion through an enlarged papilla of Vater. On the cholangiogram, the cystic lesion communicated with bile duct, and large filling defects caused by mucin were observed in the dilated common bile duct. This lesion was diagnosed as a mucin-secreting bile duct tumor. Left and caudate lobectomy of the liver with extrahepatic bile duct resection and reconstruction was performed according to the possibility of the tumor's malignant behavior. Histological examination of the specimen revealed biliary cystic wall was covered by micropapillary neoplastic epithelium with mucin secretion lacking stromal invasion nor ovarian-like stroma. The patient has remained well with no evidence of recurrence for 38 months since her operation.

CONCLUSION

It is only recently that the term "intraductal papillary mucinous neoplasm (IPMN)," which is accepted as a distinct disease entity of the pancreas, has begun to be used for mucin-secreting bile duct tumor. This case also seemed to be intraductal papillary neoplasm with prominent cystic dilatation of the bile duct.

摘要

背景

尽管胰腺导管内乳头状黏液性肿瘤(IPMN)被公认为一种独特的疾病实体,但黏液分泌性胆管肿瘤的概念尚未完全确立。

病例报告

我们在此描述一例黏液分泌性胆管肿瘤病例。影像学检查显示肝脏左外侧段有一个直径2厘米的囊性病变。十二指肠内镜检查发现通过扩大的 Vater 乳头有黏液分泌。在胆管造影中,囊性病变与胆管相通,在扩张的胆总管中观察到由黏液引起的大的充盈缺损。该病变被诊断为黏液分泌性胆管肿瘤。根据肿瘤恶性行为的可能性,进行了肝左叶和尾状叶切除术及肝外胆管切除和重建。对标本的组织学检查显示胆管囊性壁被微乳头状肿瘤上皮覆盖,有黏液分泌,无间质浸润和卵巢样间质。自手术以来,该患者已健康存活38个月,无复发迹象。

结论

直到最近,“导管内乳头状黏液性肿瘤(IPMN)”这一术语,作为胰腺的一种独特疾病实体已被接受,才开始用于黏液分泌性胆管肿瘤。该病例似乎也是伴有胆管明显囊性扩张的导管内乳头状肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af3c/2000466/6295232a7a56/1477-7819-5-98-1.jpg

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