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Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct

Intraductal papillary neoplasm of the bile duct (IPNB) has been widely recognized. However, the knowledge of intracystic papillary neoplasm of the gallbladder (IPNG) including papillary adenoma and adenocarcinoma is not well defined. In this study, we compared the clinicopathological and immunohisto...

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Autores principales: Wan, Xueshuai, Shi, Jie, Wang, Anqiang, Xie, Yuan, Yang, Xiaobo, Zhu, Chengpei, Zhang, Haohai, Wu, Liangcai, Wang, Shanshan, Huang, Hanchun, Lin, Jianzhen, Zheng, Yongchang, Liang, Zhiyong, Sang, Xinting, Zhao, Haitao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458227/
https://www.ncbi.nlm.nih.gov/pubmed/28415560
http://dx.doi.org/10.18632/oncotarget.16360
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author Wan, Xueshuai
Shi, Jie
Wang, Anqiang
Xie, Yuan
Yang, Xiaobo
Zhu, Chengpei
Zhang, Haohai
Wu, Liangcai
Wang, Shanshan
Huang, Hanchun
Lin, Jianzhen
Zheng, Yongchang
Liang, Zhiyong
Sang, Xinting
Zhao, Haitao
author_facet Wan, Xueshuai
Shi, Jie
Wang, Anqiang
Xie, Yuan
Yang, Xiaobo
Zhu, Chengpei
Zhang, Haohai
Wu, Liangcai
Wang, Shanshan
Huang, Hanchun
Lin, Jianzhen
Zheng, Yongchang
Liang, Zhiyong
Sang, Xinting
Zhao, Haitao
author_sort Wan, Xueshuai
collection PubMed
description Intraductal papillary neoplasm of the bile duct (IPNB) has been widely recognized. However, the knowledge of intracystic papillary neoplasm of the gallbladder (IPNG) including papillary adenoma and adenocarcinoma is not well defined. In this study, we compared the clinicopathological and immunohistochemical features between 32 IPNG cases and 32 IPNB cases. IPNG-1 (low-high grade dysplasia) exhibited an earlier onset age, smaller tumor size and lower level of CK20 expression compared to IPNG-2 (invasive carcinoma). Histologically, pancreaticobiliary and intestinal subtype accounted for nearly half of IPNG or IPNB (44.4% and 48.1% vs. 44.0% and 44.0%), respectively. Immunohistochemically, 88.9% of IPNG and 92.0% of IPNB cases were positive for MUC1, and 96.3% and 92.0% for CK7, respectively. CDX2 and MUC2 were more highly expressed in the intestinal subtype than in other subtypes. CK20 expression increased in parallel with tumor progression. In addition, 53.1% of IPNG cases and 68.6% of IPNB cases exhibited invasive carcinoma, and showed significant survival advantages to conventional gallbladder adenocarcinoma and cholangiocarcinoma, respectively. In conclusion, papillary adenoma and adenocarcinoma of the gallbladder can be recognized as different pathological stages of IPNG, and they share pathological features with IPNB.
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spelling pubmed-54582272017-06-08 Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct Wan, Xueshuai Shi, Jie Wang, Anqiang Xie, Yuan Yang, Xiaobo Zhu, Chengpei Zhang, Haohai Wu, Liangcai Wang, Shanshan Huang, Hanchun Lin, Jianzhen Zheng, Yongchang Liang, Zhiyong Sang, Xinting Zhao, Haitao Oncotarget Research Paper Intraductal papillary neoplasm of the bile duct (IPNB) has been widely recognized. However, the knowledge of intracystic papillary neoplasm of the gallbladder (IPNG) including papillary adenoma and adenocarcinoma is not well defined. In this study, we compared the clinicopathological and immunohistochemical features between 32 IPNG cases and 32 IPNB cases. IPNG-1 (low-high grade dysplasia) exhibited an earlier onset age, smaller tumor size and lower level of CK20 expression compared to IPNG-2 (invasive carcinoma). Histologically, pancreaticobiliary and intestinal subtype accounted for nearly half of IPNG or IPNB (44.4% and 48.1% vs. 44.0% and 44.0%), respectively. Immunohistochemically, 88.9% of IPNG and 92.0% of IPNB cases were positive for MUC1, and 96.3% and 92.0% for CK7, respectively. CDX2 and MUC2 were more highly expressed in the intestinal subtype than in other subtypes. CK20 expression increased in parallel with tumor progression. In addition, 53.1% of IPNG cases and 68.6% of IPNB cases exhibited invasive carcinoma, and showed significant survival advantages to conventional gallbladder adenocarcinoma and cholangiocarcinoma, respectively. In conclusion, papillary adenoma and adenocarcinoma of the gallbladder can be recognized as different pathological stages of IPNG, and they share pathological features with IPNB. Impact Journals LLC 2017-03-18 /pmc/articles/PMC5458227/ /pubmed/28415560 http://dx.doi.org/10.18632/oncotarget.16360 Text en Copyright: © 2017 Wan et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wan, Xueshuai
Shi, Jie
Wang, Anqiang
Xie, Yuan
Yang, Xiaobo
Zhu, Chengpei
Zhang, Haohai
Wu, Liangcai
Wang, Shanshan
Huang, Hanchun
Lin, Jianzhen
Zheng, Yongchang
Liang, Zhiyong
Sang, Xinting
Zhao, Haitao
Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title_full Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title_fullStr Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title_full_unstemmed Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title_short Gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
title_sort gallbladder papillary neoplasms share pathological features with intraductal papillary neoplasm of the bile duct
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458227/
https://www.ncbi.nlm.nih.gov/pubmed/28415560
http://dx.doi.org/10.18632/oncotarget.16360
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