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Pathological knowledge endoscopists need for the early diagnosis of pancreatic cancer Naoki Sano 1 , Noriyoshi Fukushima 1 1Department of Pathology, Jichi Medical University, Tochigi, Japan Keyword: pancreatic cancer , pathological classification , genetic alteration pp.699-709
Published Date 2024/5/25
DOI https://doi.org/10.24479/endo.0000001436

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  • Abstract
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 The majority of pancreatic cancer cases consist of invasive ductal carcinoma (IDC), i.e., pancreatic ductal adenocarcinoma, whose characteristics are marked desmoplastic stromal reactions that contribute to forming a solid mass with irregular and obscure margins. Major molecular subtypes are classical and basal-like; the former is morphologically related to well- to moderately differentiated tubular adenocarcinoma, while the latter tends to show poorly differentiated adenocarcinoma and adenosquamous carcinoma. Pancreatic intraepithelial neoplasia (PanIN) is microscopic, noninvasive, and confined to the pancreatic ducts, and is subclassified into low- and high-grade types. High-grade PanIN is equivalent to carcinoma in situ. Since the genetic alterations share similarities with IDC, PanIN is considered the main precursor lesion of IDC. Recently it has been revealed that high-grade PanIN shows focal parenchymal atrophy and fatty replacement of the pancreas, leading to early resection before the development of invasive lesions. Among intraductal papillary mucinous neoplasms (IPMNs), intestinal and pancreatobiliary types are frequently associated with invasive carcinomas, especially mucinous carcinomas and tubular carcinomas, respectively. IDC, PanIN, and IPMN may concurrently exist in the same resected pancreas. In this situation, interpreting the relationship of each lesion requires detailed examination with close clinicopathological cooperation.


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電子版ISSN 印刷版ISSN 0915-3217 東京医学社

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