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Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature
BACKGROUND: Pancreas divisum, the most common congenital anomaly of the pancreas, is caused by failure of the fusion of the ventral and dorsal pancreatic duct systems during embryological development. Although various pancreatic tumors can occur in patients with pancreas divisum, intraductal papilla...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495851/ https://www.ncbi.nlm.nih.gov/pubmed/26152300 http://dx.doi.org/10.1186/s12876-015-0313-3 |
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author | Nishi, Takeshi Kawabata, Yasunari Ishikawa, Noriyoshi Araki, Asuka Yano, Seiji Maruyama, Riruke Tajima, Yoshitsugu |
author_facet | Nishi, Takeshi Kawabata, Yasunari Ishikawa, Noriyoshi Araki, Asuka Yano, Seiji Maruyama, Riruke Tajima, Yoshitsugu |
author_sort | Nishi, Takeshi |
collection | PubMed |
description | BACKGROUND: Pancreas divisum, the most common congenital anomaly of the pancreas, is caused by failure of the fusion of the ventral and dorsal pancreatic duct systems during embryological development. Although various pancreatic tumors can occur in patients with pancreas divisum, intraductal papillary mucinous neoplasm is rare. CASE PRESENTATION: A 77-year-old woman was referred to our hospital because she was incidentally found to have a cystic tumor in her pancreas at a regular health checkup. Contrast-enhanced abdominal computed tomography images demonstrated a cystic tumor in the head of the pancreas measuring 40 mm in diameter with slightly enhancing mural nodules within the cyst. Endoscopic retrograde pancreatography via the major duodenal papilla revealed a cystic tumor and a slightly dilated main pancreatic duct with an abrupt interruption at the head of the pancreas. The orifice of the major duodenal papilla was remarkably dilated and filled with an abundant extrusion of mucin, and the diagnosis based on pancreatic juice cytology was “highly suspicious for adenocarcinoma”. Magnetic resonance cholangiopancreatography depicted a normal, non-dilated dorsal pancreatic duct throughout the pancreas. The patient underwent a pylorus-preserving pancreaticoduodenectomy under the diagnosis of intraductal papillary mucinous neoplasm with suspicion of malignancy arising in the ventral part of the pancreas divisum. A pancreatography via the major and minor duodenal papillae on the surgical specimen revealed that the ventral and dorsal pancreatic ducts were not connected, and the tumor originated in the ventral duct, i.e., the Wirsung’s duct. Microscopically, the tumor was diagnosed as intraductal papillary mucinous carcinoma with microinvasion. In addition, marked fibrosis with acinar cell depletion was evident in the ventral pancreas, whereas no fibrotic change was noted in the dorsal pancreas. CONCLUSION: Invasive ductal carcinomas of the pancreas associated with pancreas divisum usually arise from the dorsal pancreas, in which the occurrence of pancreatic cancer may link to underlying longstanding chronic pancreatitis in the dorsal pancreas; however, the histopathogenesis of intraductal papillary mucinous neoplasm in this anomaly is a critical issue that warrants further investigation in future. |
format | Online Article Text |
id | pubmed-4495851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44958512015-07-09 Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature Nishi, Takeshi Kawabata, Yasunari Ishikawa, Noriyoshi Araki, Asuka Yano, Seiji Maruyama, Riruke Tajima, Yoshitsugu BMC Gastroenterol Case Report BACKGROUND: Pancreas divisum, the most common congenital anomaly of the pancreas, is caused by failure of the fusion of the ventral and dorsal pancreatic duct systems during embryological development. Although various pancreatic tumors can occur in patients with pancreas divisum, intraductal papillary mucinous neoplasm is rare. CASE PRESENTATION: A 77-year-old woman was referred to our hospital because she was incidentally found to have a cystic tumor in her pancreas at a regular health checkup. Contrast-enhanced abdominal computed tomography images demonstrated a cystic tumor in the head of the pancreas measuring 40 mm in diameter with slightly enhancing mural nodules within the cyst. Endoscopic retrograde pancreatography via the major duodenal papilla revealed a cystic tumor and a slightly dilated main pancreatic duct with an abrupt interruption at the head of the pancreas. The orifice of the major duodenal papilla was remarkably dilated and filled with an abundant extrusion of mucin, and the diagnosis based on pancreatic juice cytology was “highly suspicious for adenocarcinoma”. Magnetic resonance cholangiopancreatography depicted a normal, non-dilated dorsal pancreatic duct throughout the pancreas. The patient underwent a pylorus-preserving pancreaticoduodenectomy under the diagnosis of intraductal papillary mucinous neoplasm with suspicion of malignancy arising in the ventral part of the pancreas divisum. A pancreatography via the major and minor duodenal papillae on the surgical specimen revealed that the ventral and dorsal pancreatic ducts were not connected, and the tumor originated in the ventral duct, i.e., the Wirsung’s duct. Microscopically, the tumor was diagnosed as intraductal papillary mucinous carcinoma with microinvasion. In addition, marked fibrosis with acinar cell depletion was evident in the ventral pancreas, whereas no fibrotic change was noted in the dorsal pancreas. CONCLUSION: Invasive ductal carcinomas of the pancreas associated with pancreas divisum usually arise from the dorsal pancreas, in which the occurrence of pancreatic cancer may link to underlying longstanding chronic pancreatitis in the dorsal pancreas; however, the histopathogenesis of intraductal papillary mucinous neoplasm in this anomaly is a critical issue that warrants further investigation in future. BioMed Central 2015-07-08 /pmc/articles/PMC4495851/ /pubmed/26152300 http://dx.doi.org/10.1186/s12876-015-0313-3 Text en © Nishi et al. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Nishi, Takeshi Kawabata, Yasunari Ishikawa, Noriyoshi Araki, Asuka Yano, Seiji Maruyama, Riruke Tajima, Yoshitsugu Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title | Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title_full | Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title_fullStr | Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title_full_unstemmed | Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title_short | Intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
title_sort | intraductal papillary mucinous carcinoma of the pancreas associated with pancreas divisum: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495851/ https://www.ncbi.nlm.nih.gov/pubmed/26152300 http://dx.doi.org/10.1186/s12876-015-0313-3 |
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