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Pathology of pancreatic cysts Kazuyuki Ishida 1 , Yumi Nozawa 1 1Department of Diagnostic Pathology, Dokkyo Medical University, Tochigi, Japan Keyword: pancreatic cystic neoplasm , intraductal neoplasm , pathologic finding pp.867-877
Published Date 2023/7/25
DOI https://doi.org/10.24479/endo.0000000797

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  • Abstract
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 Pancreatic cystic lesions are a diverse group, and this article describes the pathology of cystic neoplasms. Intraductal papillary mucinous neoplasms (IPMNs) are histologically classified as low grade or high grade and subclassified into gastric, intestinal, and pancreatobiliary types based on the predominant cell differentiation pattern. Histological subtyping is related to the extent of spread, the histological type of the invasive carcinoma, and the prognosis. IPMNs must be differentiated from intraductal oncocytic papillary neoplasms (IOPNs) and intraductal tubulopapillary neoplasms (ITPNs). Mucinous cystic neoplasms (MCNs) are mucin-producing epithelial neoplasms with ovarian-type subepithelial stroma but may have a nonmucinous epithelium of the pancreatobiliary type. Among serous neoplasms (SNs), serous cystadenomas (SCNs) are encountered more frequently and form numerous cysts composed of cuboidal or flat epithelium. Solid neoplasms that exhibit cystic changes must also be differentiated. Solid pseudopapillary neoplasms (SPNs) have pseudopapillary architecture due to degeneration. Neuroendocrine tumors (NETs) may become cystic as a result of tumor degeneration, or the spread of the tumor may affect the pancreatic duct, resulting in dilatation of the caudal pancreatic duct. To understand pancreatic cystic neoplasms, it is important to clarify whether or not they are true cysts, whether or not they originate from the pancreatic duct, and to determine the type of cells that line and proliferate in the cyst.


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電子版ISSN 印刷版ISSN 0915-3217 東京医学社

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