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Basic pancreatic lesions: Radiologic-pathologic correlation

<!DOCTYPE html> <html lang="en" xmlns:mml="http://www.w3.org/1998/Math/MathML"> <head> <meta charset="utf-8"> <meta http-equiv="x-ua-compatible" content="ie=edge"> <title>Basic pancreatic lesions: Radiologic-pathologic correlation</title> <!-- Preload Montserrat Fonts --> <link rel="preload" href="/assets/fonts/montserrat-v15-latin-ext_cyrillic-ext-regular.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <link rel="preload" href="/assets/fonts/montserrat-v25-latin-ext_cyrillic-ext-500.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <link rel="preload" href="/assets/fonts/montserrat-v15-latin-ext_cyrillic-ext-700.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <!-- Preload Merriweather Fonts --> <link rel="preload" href="/assets/fonts/merriweather-v30-latin-ext_cyrillic-ext-300.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <link rel="preload" href="/assets/fonts/merriweather-v22-latin-ext_cyrillic-ext-regular.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <link rel="preload" href="/assets/fonts/merriweather-v22-latin-ext_cyrillic-ext-700.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <!-- Preload Font Awesome --> <link rel="preload" href="/assets/stylesheets/fontawesome.woff2" as="font" type="font/woff2" crossorigin="anonymous"> <link rel="stylesheet" media="all" href='/assets/stylesheets/02f295d1f6a8e9c282e7831cd493e8ff-bootstrap.purged.min.css' /> <link rel="stylesheet" media="all" href='/assets/stylesheets/5337b0511e7530e28f005276f70cde44-main.min.css' /> <link rel="stylesheet" media="all" href='/assets/stylesheets/13761c60ba5201f465803f3005ccd7ef-fontawesome-codes.css' /> <link rel="shortcut icon" type="image/x-icon" href='/assets/images/ec7d7606b4e2f3f921b5e1700948efb6-favicon.ico' /> <link rel="alternate" hreflang="en" href="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/html?lang=en" /> <link rel="alternate" hreflang="de" href="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/html?lang=de" /> <link rel="alternate" hreflang="x-default" href="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/html" /> <!--[if le IE 11]> <script nonce="UqdhW8mFEkTMtbscWyW7Dw==" src='/assets/javascripts/2568c6be22833eac0f750ff472b3caf0-polyfill.min.js'></script> <![endif]--> <link rel="schema.dcterms" href="http://purl.org/dc/terms/"> <meta name="dcterms.rightsHolder" content="Walter de Gruyter GmbH"> <meta name="dcterms.rights" content="De Gruyter expressly reserves the right to use all content for commercial text and data mining within the meaning of Section 44b of the German Copyright Act."> <link rel="dns-prefetch" href="https://www.google-analytics.com" /> <meta name="google" content="notranslate" /> <meta name="viewport" content="width=device-width, initial-scale=1" /> <meta name="description" content="The basic pancreatic lesions include location, size, shape, number, capsule, calcification/calculi, hemorrhage, cystic degeneration, fibrosis, pancreatic duct alterations, and microvessel. One or more basic lesions form a kind of pancreatic disease. As recognizing the characteristic imaging features of pancreatic basic lesions and their relationships with pathology aids in differentiating the variety of pancreatic diseases. The purpose of this study is to review the pathological and imaging features of the basic pancreatic lesions."/> <meta property="og:url" content="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/html"/><meta property="og:site_name" content="De Gruyter"/><meta property="og:title" content="Basic pancreatic lesions: Radiologic-pathologic correlation"/><meta property="og:type" content="article"/><meta property="og:locale" content="en"/><meta property="og:image" content="https://www.degruyter.com/document/cover/journal_key/JTIM/product"/><meta property="og:image:type" content="image/jpeg"/><meta property="og:description" content="The basic pancreatic lesions include location, size, shape, number, capsule, calcification/calculi, hemorrhage, cystic degeneration, fibrosis, pancreatic duct alterations, and microvessel. One or more basic lesions form a kind of pancreatic disease. As recognizing the characteristic imaging features of pancreatic basic lesions and their relationships with pathology aids in differentiating the variety of pancreatic diseases. The purpose of this study is to review the pathological and imaging features of the basic pancreatic lesions."/><meta property="og:locale:alternate" content="de"/><meta property="article:author" content="Yun Bian"/><meta property="article:author" content="Hui Jiang"/><meta property="article:author" content="Jianming Zheng"/><meta property="article:author" content="Chengwei Shao"/><meta property="article:author" content="Jianping Lu"/><meta property="article:tag" content="pancreatic diseases"/><meta property="article:tag" content="pancreatic neoplasms"/><meta property="article:tag" content="pancreatitis"/><meta property="article:tag" content="pancreatic ducts"/><meta property="article:tag" content="magnetic resonance imaging"/><meta property="article:tag" content="computed tomography"/><meta property="article:tag" content="radiology"/><meta property="article:tag" content="pathology"/><meta property="article:published_time" content="2022-03-01"/><meta property="article:section" content="Journal of Translational Internal Medicine"/> <meta name="citation_firstpage" content="18" /> <meta name="citation_lastpage" content="27" /> <meta name="citation_issue" content="1" /> <meta name="citation_issn" content="2224-4018" /> <meta name="citation_language" content='en' /> <meta name="citation_volume" content="10" /> <meta name="citation_publisher" content='De Gruyter' /> <meta name="citation_pdf_url" content="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/pdf" /> <meta name="citation_keywords" content='pancreatic diseases; pancreatic neoplasms; pancreatitis; pancreatic ducts; magnetic resonance imaging; computed tomography; radiology; pathology' /> <meta name="citation_author" content="Yun Bian" /> <meta name="citation_author" content="Hui Jiang" /> <meta name="citation_author" content="Jianming Zheng" /> <meta name="citation_author" content="Chengwei Shao" /> <meta name="citation_author" content="Jianping Lu" /> <meta name="citation_title" content='Basic pancreatic lesions: Radiologic-pathologic correlation' /> <meta name="citation_xml_url" content="https://www.degruyter.com/document/doi/10.2478/jtim-2022-0003/xml" /> <meta name="citation_journal_title" content="Journal of Translational Internal Medicine" /> <meta name="citation_publication_date" content='2022/03/01' /> <meta name="citation_doi" content="10.2478/jtim-2022-0003" /> <meta name="citation_fulltext_world_readable" content="" /> <script type="application/ld+json">{"author":[{"@type":"Person","name":"Yun Bian"},{"@type":"Person","name":"Hui Jiang"},{"@type":"Person","name":"Jianming Zheng"},{"@type":"Person","name":"Chengwei Shao"},{"@type":"Person","name":"Jianping Lu"}],"editor":[],"audience":null,"datePublished":"2022-03-01","headline":"","keywords":"keyword,keyword,keyword,keyword,keyword,keyword,keyword,keyword","isAccessibleForFree":true,"publisher":{"@type":"Organization","name":"De Gruyter"},"@context":"https://schema.org","@type":"Article","name":"Basic pancreatic lesions: Radiologic-pathologic correlation","image":"https://www.degruyter.com/document/cover/journal_key/JTIM/thumbnail","url":"https://doi.org/10.2478/jtim-2022-0003"}</script> <script nonce="UqdhW8mFEkTMtbscWyW7Dw=="> // Define dataLayer and the gtag function. window.dataLayer = window.dataLayer || []; function gtag(){dataLayer.push(arguments);} function getCookieValue(name){ const regex = new RegExp(`(^| )${name}=([^;]+)`) const match = document.cookie.match(regex) if (match) { return match[2] } } // Set default consent to 'denied' as a placeholder // Determine actual values based on your own requirements const acceptCookies = getCookieValue('acceptcookies') === "true"; const defaultSettings = (acceptCookies) => ({ 'ad_storage': acceptCookies ? 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Your documents are now available to view.</p> <div id="orderCompleteItemList"> </div> </div> </div> </div> </div> <main id="main" class='language_en min-vh-100 '> <div class="row no-theme-gutter-x g-0 " id="docContent"> <div class='offset-lg-1 col-lg-8 pb-2'> <div class='row g-0 '> <div class="col p-3 pt-5"> <div class="d-flex flex-wrap flex-column flex-md-row justify-content-between"> <div> <div class="mb-2"> <span> <a class="creative-commons-license ga_creative_commons_license text-decoration-none" href="https://creativecommons.org/licenses/by-nc-nd/3.0/" title='Creative Commons - Some Rights Reserved'> <img src="/assets/images/cc-licenses/by-nc-nd.eu.svg" height="100%" width="100%" alt='BY-NC-ND 3.0 license'/> </a> </span> <span class="fa fas fa-icon-open-access"></span> <span class="accessOpenAccess me-2">Open Access</span> <span class="publisherAndPublicationDate metadataInfoMainContent"> <span class="publisher"> Published by <a class="ga_published_by ga_published_by_header" href='/search?query=*&amp;publisherFacet=De+Gruyter'>De Gruyter</a> </span> <span class="publicationDate">April 2, 2022</span> </span> </div> <div id="mobilePurchaseDiv" class="d-none"> <a class="mobilePurchaseButton" href="#"> Purchase article <svg width="17" height="16" viewBox="0 0 17 16" fill="none" xmlns="http://www.w3.org/2000/svg"> <path fill-rule="evenodd" clip-rule="evenodd" d="M12.75 10.3238L11.4513 9L9.5 11.1469L9.5 1L7.5 1L7.5 11.1473L5.54829 9L4.24962 10.3238L8.49981 15L12.75 10.3238Z" fill="#007596"/> </svg> </a> </div> <h1>Basic pancreatic lesions: Radiologic-pathologic correlation</h1> <ul class="contributors list-unstyled mb-2"> <li class="contributors-AUTHOR mb-2"> <span class="metadataAndContributorsFont"><span class="contributor"> <span class="displayName linkAnimation">Yun Bian</span> <contributor-popdown name="Yun Bian" position="1" email="" affiliations="Department of Radiology, Changhai Hospital, The Naval Medical University, Shanghai 200433, China" > </contributor-popdown> </span><span class="comma">, </span><span class="contributor"> <span class="displayName linkAnimation">Hui Jiang</span> <contributor-popdown name="Hui Jiang" position="2" email="" affiliations="Department of Pathology, Changhai Hospital, The Naval Medical University, Shanghai 200433, China" > </contributor-popdown> </span><span class="comma">, </span><span class="contributor"> <span class="displayName linkAnimation">Jianming Zheng</span> <contributor-popdown name="Jianming Zheng" position="3" email="" affiliations="Department of Pathology, Changhai Hospital, The Naval Medical University, Shanghai 200433, China" > </contributor-popdown> </span><span class="comma">, </span><span class="contributor"> <span class="displayName linkAnimation">Chengwei Shao</span> <contributor-popdown name="Chengwei Shao" position="4" email="" affiliations="Department of Radiology, Changhai Hospital, The Naval Medical University, Shanghai 200433, China" > </contributor-popdown> </span> and <span class="contributor"> <span class="displayName linkAnimation">Jianping Lu</span> <contributor-popdown name="Jianping Lu" position="5" email="cjr.lujianping@vip.163.com" affiliations="Department of Radiology, Changhai Hospital, The Naval Medical University, Shanghai 200433, China" > </contributor-popdown> <a href="mailto:cjr.lujianping@vip.163.com"> <img alt="EMAIL logo" src='/assets/images/db2546a9d03b905bae083962a41791e1-mail.svg' width="16" height="12" /> </a> </span></span> </li> </ul> <div class="subTitleInfoProductPage">From the journal <a class="ga_parent ga_parent_journal" href="/journal/key/jtim/html">Journal of Translational Internal Medicine</a></div> <div class="doi"><a href="https://doi.org/10.2478/jtim-2022-0003" class="linkWithoutStyle subTitleInfoProductPage ga_doi" target="_blank">https://doi.org/10.2478/jtim-2022-0003</a></div> </div> <div class="d-sm-none pt-3 pb-3 border-bottom"> <div class="alternateForms d-none"> <a 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data-doi="10.2478/jtim-2022-0003" data-hide-zero-citations="true" data-legend="never" data-style="large_rectangle"></div> </div> <div id="div-document-progress-bar" class="sticky-top d-none"> <div class="row"> <div class="col-12"> <div class="progress progress-bar-toolbar"> <div id="document-progress-bar" class="progress-bar bg-primary" role="progressbar" aria-label="Document progress bar" aria-valuenow="0" aria-valuemin="0" aria-valuemax="100"></div> </div> </div> </div> </div> <div id="document-main-content" class='row'> <div class="container-fluid px-3 px-lg-0 py-2"> <div class="col"> <div class="d-none analyticsHolder" data-subjects='MD|MD-04|MD-04-03|MD-04-03-01|MD-04-03-02|MD-04-03-03|MD-04-03-07' data-publisherCode='DEG' data-license='open-access' data-publisher='De Gruyter' data-contentName='Basic pancreatic lesions: Radiologic-pathologic correlation' data-doi='10.2478/jtim-2022-0003' data-parentIdentifier='JTIM' data-parentName='Journal of Translational Internal Medicine' data-languages='en' ></div> <div id="documentContent" class="content py-2" data-doi='10.2478/jtim-2022-0003' data-accessrestricted="false" data-countertype="document"> <div class="px-2"> <div id="text-container"> <div xmlns:dgdoi="http://degruyter.com/resources/doi-from-crossref" xmlns:dgpm="http://degruyter.com/resources/fetched-pubmed-id" class="contentWrapper"><div class="article" lang="en"><div class="abstract"> <h2 class="subheading">Abstract</h2> <p>The basic pancreatic lesions include location, size, shape, number, capsule, calcification/calculi, hemorrhage, cystic degeneration, fibrosis, pancreatic duct alterations, and microvessel. One or more basic lesions form a kind of pancreatic disease. As recognizing the characteristic imaging features of pancreatic basic lesions and their relationships with pathology aids in differentiating the variety of pancreatic diseases. The purpose of this study is to review the pathological and imaging features of the basic pancreatic lesions.</p></div><div class="keywords mb-3">Key words: <a href="/search?query=keywordValues%3A%28%22pancreatic%20diseases%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">pancreatic diseases</a>; <a href="/search?query=keywordValues%3A%28%22pancreatic%20neoplasms%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">pancreatic neoplasms</a>; <a href="/search?query=keywordValues%3A%28%22pancreatitis%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">pancreatitis</a>; <a href="/search?query=keywordValues%3A%28%22pancreatic%20ducts%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">pancreatic ducts</a>; <a href="/search?query=keywordValues%3A%28%22magnetic%20resonance%20imaging%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">magnetic resonance imaging</a>; <a href="/search?query=keywordValues%3A%28%22computed%20tomography%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">computed tomography</a>; <a href="/search?query=keywordValues%3A%28%22radiology%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">radiology</a>; <a href="/search?query=keywordValues%3A%28%22pathology%22%29%20AND%20journalKey%3A%28%22JTIM%22%29&amp;documentVisibility=all&amp;documentTypeFacet=article" class="ga_keyword">pathology</a></div><div class="body"> <section id="j_jtim-2022-0003_s_001"><h2 class="subheading">Introduction</h2> <p>The pancreas is an important organ in the human body, consisting of two organs in one: an exocrine gland and an endocrine gland.<sup>[<a href="#j_jtim-2022-0003_ref_001" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_001" data-bs-toggle="tooltip" title="1 Leung PS. Overview of the pancreas. Adv Exp Med Biol 2010;690:3-12.10.1007/978-90-481-9060-7_1Search in Google Scholar">1</a>]</sup> Pathological characteristics of basic pancreatic lesions include location, size, shape, number, capsule, calcification/ calculi, cystic degeneration, fibrosis, duct alterations, and microvessel.<sup>[<a href="#j_jtim-2022-0003_ref_002" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_002" data-bs-toggle="tooltip" title="2 Al-Hawary MM, Francis IR, Chari ST, Fishman EK, Hough DM, Lu DS, et al. Pancreatic ductal adenocarcinoma radiology reporting template: consensus statement of the Society of Abdominal Radiology and the American Pancreatic Association. Gastroenterology 2014;146:291-304. e1.10.1053/j.gastro.2013.11.004Search in Google Scholar">2</a>,<a href="#j_jtim-2022-0003_ref_003" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_003" data-bs-toggle="tooltip" title="3 Al-Hawary MM, Francis IR, Chari ST, Fishman EK, Hough DM, Lu DS, et al. Pancreatic ductal adenocarcinoma radiology reporting template: consensus statement of the Society of Abdominal Radiology and the American Pancreatic Association. Radiology 2014;270:248-60.10.1148/radiol.13131184Search in Google Scholar">3</a>]</sup> These pathological characteristics are reflected in radiological images. The spectrum of pancreatic diseases is extensive, including pancreatitis and neoplasm. Chronic pancreatitis (CP) and serous cystic neoplasm (SCN) are characterized by calcification. Pancreatic calcification/ calculi in CP are mostly found in the main ducts, side branches, or parenchyma.<sup>[<a href="#j_jtim-2022-0003_ref_004" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_004" data-bs-toggle="tooltip" title="4 Beyer G, Habtezion A, Werner J, Lerch MM, Mayerle J. Chronic pancreatitis. Lancet 2020;396:499-512.10.1016/S0140-6736(20)31318-0Search in Google Scholar">4</a>,<a href="#j_jtim-2022-0003_ref_005" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_005" data-bs-toggle="tooltip" title="5 Anaizi A, Hart PA, Conwell DL. Diagnosing Chronic Pancreatitis. Dig Dis Sci 2017;62:1713-20.10.1007/s10620-017-4493-2Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">5</a>]</sup> SCN is characterized by the typical central stellate scar that calcium is frequently shown.<sup>[<a href="#j_jtim-2022-0003_ref_006" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_006" data-bs-toggle="tooltip" title="6 van Huijgevoort NCM, Del Chiaro M, Wolfgang CL, van Hooft JE, Besselink MG. Diagnosis and management of pancreatic cystic neoplasms: current evidence and guidelines. Nat Rev Gastroenterol Hepatol 2019;16:676-89.10.1038/s41575-019-0195-xSearch in Google Scholar&#xA; PubMed&#xA; ">6</a>]</sup> Hemorrhage mainly occurs in solid-pseudopapillary neoplasm (SPN).<sup>[<a href="#j_jtim-2022-0003_ref_007" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_007" data-bs-toggle="tooltip" title="7 Anil G, Zhang J, Al Hamar NE, Nga ME. Solid pseudopapillary neoplasm of the pancreas: CT imaging features and radiologic-pathologic correlation. Diagn Interv Radiol 2017;23:94-9.10.5152/dir.2016.16104Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">7</a>]</sup> CP and pancreatic ductal adenocarcinoma (PDAC) are characterized by pancreatic duct alterations.<sup>[<a href="#j_jtim-2022-0003_ref_008" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_008" data-bs-toggle="tooltip" title="8 Bowman AW, Bolan CW. MRI evaluation of pancreatic ductal adenocarcinoma: diagnosis, mimics, and staging. Abdom Radiol (NY) 2019;44:936-49.10.1007/s00261-018-1686-xSearch in Google Scholar&#xA; PubMed&#xA; ">8</a>,<a href="#j_jtim-2022-0003_ref_009" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_009" data-bs-toggle="tooltip" title="9 Wolske KM, Ponnatapura J, Kolokythas O, Burke LMB, Tappouni R, Lalwani N. Chronic Pancreatitis or Pancreatic Tumor? A Problem-solving Approach. Radiographics 2019;39:1965-82.10.1148/rg.2019190011Search in Google Scholar&#xA; PubMed&#xA; ">9</a>]</sup> “String of pearls” appearance of main duct is found in CP.<sup>[<a href="#j_jtim-2022-0003_ref_010" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_010" data-bs-toggle="tooltip" title="10 Nuernberg D, Ignee A, Dietrich CF. Ultrasound in gastroenterology. Biliopancreatic system. Med Klin (Munich) 2007;102:112-26.10.1007/s00063-007-1003-xSearch in Google Scholar&#xA; PubMed&#xA; ">10</a>]</sup> “Double-duct sign” or “cutoff sign” is found in PDAC.<sup>[<a href="#j_jtim-2022-0003_ref_011" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_011" data-bs-toggle="tooltip" title="11 Elsherif SB, Virarkar M, Javadi S, Ibarra-Rovira JJ, Tamm EP, Bhosale PR. Pancreatitis and PDAC: association and differentiation. Abdom Radiol (NY) 2020;45:1324-37.10.1007/s00261-019-02292-wSearch in Google Scholar&#xA; PubMed&#xA; ">11</a>]</sup> In pancreatic cystic neoplasms, SCN was mainly multilocular and multiseptal,<sup>[<a href="#j_jtim-2022-0003_ref_012" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_012" data-bs-toggle="tooltip" title="12 Antonini F, Fuccio L, Fabbri C, Macarri G, Palazzo L. Management of serous cystic neoplasms of the pancreas. Expert Rev Gastroenterol Hepatol 2015;9:115-25.10.1586/17474124.2014.934675Search in Google Scholar&#xA; PubMed&#xA; ">12</a>]</sup> while mucinous cystic neoplasm (MCN) was mainly large and unilocular,<sup>[<a href="#j_jtim-2022-0003_ref_013" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_013" data-bs-toggle="tooltip" title="13 Burk KS, Knipp D, Sahani DV. Cystic Pancreatic Tumors. Magn Reson Imaging Clin N Am 2018;26:405-20.10.1016/j.mric.2018.03.006Search in Google Scholar&#xA; PubMed&#xA; ">13</a>]</sup> and Intraductal papillary mucinous tumors (IPMN) is communicated with the main duct.<sup>[<a href="#j_jtim-2022-0003_ref_014" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_014" data-bs-toggle="tooltip" title="14 Yadav RK, Jiang X, Chen J. Differentiating benign from malignant pancreatic cysts on computed tomography. Eur J Radiol Open 2020;7:100278.10.1016/j.ejro.2020.100278Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">14</a>]</sup> The blood supply of the lesion is also a key clue to our diagnosis. Most pancreatic neuroendocrine tumors (pNETs) are significantly enhanced in late arterial or portal phase,<sup>[<a href="#j_jtim-2022-0003_ref_015" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_015" data-bs-toggle="tooltip" title="15 Dromain C, Deandreis D, Scoazec JY, Goere D, Ducreux M, Baudin E, et al. Imaging of neuroendocrine tumors of the pancreas. Diagn Interv Imaging 2016;97:1241-57.10.1016/j.diii.2016.07.012Search in Google Scholar&#xA; PubMed&#xA; ">15</a>]</sup> while most PDAC shows no significant enhancement or the mild progressive enhancement.</p> <p>However, radiologists start to analyzes the imaging findings of various basic pancreatic lesions and then combine these imaging findings with the relevant pathological characteristics to give the final diagnosis. So, it is very important to understand the pathological mechanism and imaging findings of the basic pancreatic lesions for the accurate diagnosis of pancreatic diseases. However, previous literatures have focused on the imaging findings of a pancreatic disease. Therefore, the main purpose of this paper is to comprehensively review the pathologic and radiologic characteristics of the basic pancreatic lesions and improve the understanding of these common pancreatic diseases.</p> </section> <section id="j_jtim-2022-0003_s_002"><h2 class="subheading">Location</h2> <p>The pancreas is divided into the head, neck, body, and tail.<sup>[<a href="#j_jtim-2022-0003_ref_016" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_016" data-bs-toggle="tooltip" title="16 Talathi SS, Zimmerman R, Young M. Anatomy, Abdomen and Pelvis, Pancreas. In: StatPearls. Treasure Island (FL) 2021.Search in Google Scholar">16</a>]</sup> The pancreatic head is located at the right margin of the superior mesenteric vein-portal vein (SMV-PV) confluence; the pancreatic body is located between the SMV-PV confluence and the left margin of the abdominal aorta; the pancreatic tail is located between the left margin of the abdominal aorta and splenic hilum.<sup>[<a href="#j_jtim-2022-0003_ref_017" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_017" data-bs-toggle="tooltip" title="17 Standring S: Gray’s Anatomy-The Anatomical Basis of Clinical Practice. 41rd ed. London: Elsevier 2016.Search in Google Scholar">17</a>]</sup> PDAC, mass-forming pancreatitis (MFP), and serous SCN occur predominantly in the head of the pancreas. Branch duct-IPMN (BD-IPMN) is commonly found in the uncinate process,<sup>[<a href="#j_jtim-2022-0003_ref_018" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_018" data-bs-toggle="tooltip" title="18 Maker AV, Maker VK. Isolated Pancreatic Uncinate Duct IPMN. J Gastrointest Surg 2017;21:744-5.10.1007/s11605-017-3380-7Search in Google Scholar&#xA; PubMed&#xA; ">18</a>]</sup> while SPN and MCN are more frequently found in the body and tail of the pancreas.</p> </section> <section id="j_jtim-2022-0003_s_003"><h2 class="subheading">Size</h2> <p>The size of a mass depends on its location, nature (benign or malignant), and functionality. Masses in the pancreatic head are often smaller at diagnosis than those in the pancreatic body and tail due to narrow growth spaces and their tendency to cause pancreaticobiliary obstruction. Masses with higher degrees of malignancy (such as PDAC) often cause abdominal pain, lower back pain, weight loss, and elevation of tumor markers (such as carbohydrate antigen 19-9); they are also usually smaller at diagnosis than benign or low-grade malignant tumors (such as SCN, SPN, and MCN). Functional pancreatic tumors, such as functional pNET, are often smaller at diagnosis because of their unique clinical symptoms resulting from hormone releases.<sup>[<a href="#j_jtim-2022-0003_ref_019" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_019" data-bs-toggle="tooltip" title="19 Lee L, Ito T, Jensen RT. Prognostic and predictive factors on overall survival and surgical outcomes in pancreatic neuroendocrine tumors: recent advances and controversies. Expert Rev Anticancer Ther 2019;19:1029-50.10.1080/14737140.2019.1693893Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">19</a>]</sup></p> </section> <section id="j_jtim-2022-0003_s_004"><h2 class="subheading">Shape and number</h2> <p>Pancreatic masses may be circular, circle-like, or lobulated. Most are unifocal; multifocal masses are relatively rare and mainly develop in cases involving pNET-associated syndromes, BD-IPMN or mixed-IPMN, von Hippel-Lindau (VHL) syndrome,<sup>[<a href="#j_jtim-2022-0003_ref_020" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_020" data-bs-toggle="tooltip" title="20 Mikhail MI, Singh AK. Von Hippel Lindau Syndrome In: StatPearls. Treasure Island (FL) 2021.Search in Google Scholar">20</a>]</sup> SPN, and pancreatic metastases.<sup>[<a href="#j_jtim-2022-0003_ref_021" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_021" data-bs-toggle="tooltip" title="21 Sellner F. Isolated Pancreatic Metastases of Renal Cell Carcinoma-A Paradigm of a Seed and Soil Mechanism: A Literature Analysis of 1,034 Observations. Front Oncol 2020;10:709.10.3389/fonc.2020.00709Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">21</a>]</sup></p> </section> <section id="j_jtim-2022-0003_s_005"><h2 class="subheading">Capsule</h2> <p>Tumor capsules, a fibrous membrane surrounding the tumor, can be categorized as either true capsules or pseudocapsules. The former is inherent, while the latter are fibroplasia as a result of slow tumor growth and compression of the surrounding tissues. Most true capsules are observed in rare pancreatic tumors such as pancreatic schwannoma, lipoma, leiomyosarcoma, solitary fibrous tumor, hamartoma, and perivascular epithelioid cell tumor. Pseudocapsules, on the other hand, are frequently found in cases of pNET and SPN. The majority of highly invasive masses, such as PDAC and adenosquamous carcinoma, lack capsules. Generally, a tumor with an intact capsule shows a clear separation from the peripheral pancreatic tissues, whereas a tumor without a capsule shows invasive growth and unclear separation from its peripheral pancreatic tissues. Capsular changes also reflect the pathological process of disease progression. For instance, the disruption of an initially intact capsule indicates that the tumor tends to become malignant, as it has penetrated the capsule and shows an invasive growth pattern.</p> <p>Despite differences in the mechanisms of formation, both true capsules and pseudocapsules are fibrous capsules and thus show low attenuation on unenhanced multislice computed tomography (MSCT), hypointense signals on T1WI, and iso-hyperintense signals on T2WI with delayed postcontrast enhancement.</p> </section> <section id="j_jtim-2022-0003_s_006"><h2 class="subheading">Pancreatic calcification/Calculi</h2> <p>Calcification caused by pancreatic diseases is considered dystrophic calcification; it implies the abnormal deposition of calcium salts in degenerated, necrotic tissues or foreign body granulomas.<sup>[<a href="#j_jtim-2022-0003_ref_022" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_022" data-bs-toggle="tooltip" title="22 Kumar V, Abbas AK, Aster JC. Robbins Basic Pathology. 9rd ed. Canada: Elsevier 2013.Search in Google Scholar">22</a>]</sup> Pancreatic calcification/calculi are mostly located in the side branches, main ducts, or parenchyma in the cases of CP.<sup>[<a href="#j_jtim-2022-0003_ref_023" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_023" data-bs-toggle="tooltip" title="23 Tandan M, Talukdar R, Reddy DN. Management of Pancreatic Calculi: An Update. Gut Liver 2016;10:873-80.10.5009/gnl15555Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">23</a>]</sup> Pancreatic stone protein (PSP) plays a vital role in the formation of calcification. Reduced PSP leads to supersaturation of calcium carbonate in the pancreatic juice.<sup>[<a href="#j_jtim-2022-0003_ref_024" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_024" data-bs-toggle="tooltip" title="24 Jin CX, Naruse S, Kitagawa M, Ishiguro H, Kondo T, Hayakawa S, et al. Pancreatic stone protein of pancreatic calculi in chronic calcified pancreatitis in man. JOP 2002;3:54-61.Search in Google Scholar">24</a>]</sup> Calcification is also often found in cases of MFP and pancreatic pseudocyst (PPC). Calcification with MFP results from CP. PPC consists mainly of mature granulation and fibrous connective tissues. In contrast, calcification in PPCs is more frequently observed in patients with a longer history of CP and may lead to calcium deposition on cystic walls. In colloid carcinomas, the thick jelly-like mucus inside is prone to calcification. Calcium deposition due to hemorrhage and poor absorption by necrotic tissues may lead to calcification in the SPN. Calcification in pNETs is similar to that in the SPN and may be associated with hormone secretion. Calcification in the MCN is commonly found on cyst walls and in the intercapsular septa, and it is characterized by lamellar calcification.<sup>[<a href="#j_jtim-2022-0003_ref_025" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_025" data-bs-toggle="tooltip" title="25 Pederzoli P, Bassi C. Uncommon Pancreatic Neoplasms. Italia: Springer 2013.10.1007/978-88-470-2673-5Search in Google Scholar">25</a>]</sup> Calcification in the SCN is often found in polycystic lesions and is characterized by the typical central stellate scar with calcium deposits (<a href="#j_jtim-2022-0003_fig_001" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_001">Figure 1</a>).<sup>[<a href="#j_jtim-2022-0003_ref_012" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_012" data-bs-toggle="tooltip" title="12 Antonini F, Fuccio L, Fabbri C, Macarri G, Palazzo L. Management of serous cystic neoplasms of the pancreas. Expert Rev Gastroenterol Hepatol 2015;9:115-25.10.1586/17474124.2014.934675Search in Google Scholar&#xA; PubMed&#xA; ">12</a>,<a href="#j_jtim-2022-0003_ref_026" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_026" data-bs-toggle="tooltip" title="26 Sakorafas GH, Smyrniotis V, Reid-Lombardo KM, Sarr MG. Primary pancreatic cystic neoplasms revisited. Part I: serous cystic neoplasms. Surg Oncol 2011;20:e84-92.10.1016/j.suronc.2010.12.002Search in Google Scholar&#xA; PubMed&#xA; ">26</a>,<a href="#j_jtim-2022-0003_ref_027" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_027" data-bs-toggle="tooltip" title="27 Sugawara S, Watanabe T, Hirai I, Fujimoto H, Kimura W. Serous cystic neoplasms. Nihon Rinsho 2015;73:298-304.Search in Google Scholar">27</a>]</sup></p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_001"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_001.jpg" alt="Figure 1 Serous cystic neoplasm of the pancreas in a 38-year-old woman. (A) Surgical specimen (distal pancreatectomy): serous cystic neoplasm with typical microcystic appearance and central scar (arrow). (B) Axial nonenhanced computed tomography image shows a cystic mass with central calcification, known as the “sunburst” sign (arrow)."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 1</span></div><div class="figure-caption mb-2"><span class="caption"><p>Serous cystic neoplasm of the pancreas in a 38-year-old woman. (A) Surgical specimen (distal pancreatectomy): serous cystic neoplasm with typical microcystic appearance and central scar (arrow). (B) Axial nonenhanced computed tomography image shows a cystic mass with central calcification, known as the “sunburst” sign (arrow).</p></span></div></div></div></div> <p>Unenhanced CT is the most sensitive imaging modality for detecting calcification/calculi, which are characterized by “hyper attenuation.”</p> </section> <section id="j_jtim-2022-0003_s_007"><h2 class="subheading">Hemorrhage</h2> <p>The disruption of blood vessels by inflammation and tumors and the fragility of blood vessels may lead to hemorrhage. Massive infiltration of inflammatory cells during acute pancreatitis (AP) may result in the rupture of blood vessels and hemorrhage.<sup>[<a href="#j_jtim-2022-0003_ref_028" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_028" data-bs-toggle="tooltip" title="28 Tang MY, Chen TW, Bollen TL, Wang YX, Xue HD, Jin ZY, et al. MR imaging of hemorrhage associated with acute pancreatitis. Pancreatology 2018;18:363-9.10.1016/j.pan.2018.03.004Search in Google Scholar&#xA; PubMed&#xA; ">28</a>]</sup> The SPN is most prone to hemorrhage, as it mainly contains fragile blood vessels, which is the stalks of the pseudopapillae.<sup>[<a href="#j_jtim-2022-0003_ref_029" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_029" data-bs-toggle="tooltip" title="29 Zhan H, Cheng Y, Wang L, Su P, Zhong N, Zhang Z, et al. Clinicopathological Features and Treatment Outcomes of Solid Pseudopapillary Neoplasms of the Pancreas: A 10-Year Case Series from a Single Center. J Laparoendosc Adv Surg Tech A 2019.10.1089/lap.2018.0704Search in Google Scholar&#xA; PubMed&#xA; ">29</a>, <a href="#j_jtim-2022-0003_ref_030" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_030" data-bs-toggle="tooltip" title="30 Beltrame V, Pozza G, Dalla Bona E, Fantin A, Valmasoni M, Sperti C. Solid-Pseudopapillary Tumor of the Pancreas: A Single Center Experience. Gastroenterol Res Pract 2016;2016:4289736.10.1155/2016/4289736Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">30</a>, <a href="#j_jtim-2022-0003_ref_031" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_031" data-bs-toggle="tooltip" title="31 Wright MJ, Javed AA, Saunders T, Zhu Y, Burkhart RA, Yu J, et al. Surgical Resection of 78 Pancreatic Solid Pseudopapillary Tumors: a 30-Year Single Institutional Experience. J Gastrointest Surg 2019.10.1007/s11605-019-04252-7Search in Google Scholar&#xA; PubMed&#xA; ">31</a>]</sup> The fragile, thin-walled blood vessels lack a strong support structure and rupture when tumor cells detach (<a href="#j_jtim-2022-0003_fig_002" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_002">Figure 2A, B)</a>. The majority of pNETs consist of well-differentiated tumor cells and abundant stromal blood vessels, which form a dense network of capillaries that may lead to intratumoral hemorrhage following rupture of blood vessels destroyed by tumor cells. In the solid mass, there are large of cells, separated by thin stroma and small blood vessels in an acinar cell carcinoma of the pancreas (ACCP).<sup>[<a href="#j_jtim-2022-0003_ref_032" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_032" data-bs-toggle="tooltip" title="32 Chaudhary P. Acinar Cell Carcinoma of the Pancreas. A Literature Review and Update. Indian J Surg 2015;77:226-31.10.1007/s12262-014-1049-ySearch in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">32</a>,<a href="#j_jtim-2022-0003_ref_033" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_033" data-bs-toggle="tooltip" title="33 La Rosa S, Sessa F, Capella C. Acinar Cell Carcinoma of the Pancreas: Overview of Clinicopathologic Features and Insights into the Molecular Pathology. Front Med (Lausanne) 2015;2:41.10.3389/fmed.2015.00041Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">33</a>]</sup> ACCP is thus prone to hemorrhage.<sup>[<a href="#j_jtim-2022-0003_ref_034" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_034" data-bs-toggle="tooltip" title="34 Campbell F, Verbeke CS. Pathology of the Pancreas. London: Springer 2013.10.1007/978-1-4471-2449-8Search in Google Scholar">34</a>]</sup> Inflammation caused by PDAC disrupts surrounding blood vessels and may also lead to intratumoral hemorrhage (<a href="#j_jtim-2022-0003_fig_002" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_002">Figure 2C, D)</a>. The SCN is characterized by the secretion of a clear, serous fluid, but secretion of blood-stained fluids can also be observed within the cystic cavities. MR T1WI is the most sensitive imaging modality for detecting hemorrhage, which is characterized by a “hyperintense signal.”</p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_002"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_002.jpg" alt="Figure 2 (A, B) Hemorrhage caused by solid-pseudopapillary neoplasm of the pancreas in an 18-year-old woman. (A) Microscopically, a large well-demarcated lesion with large hemorrhage. (B) Axial T1-weighted fat-saturated magnetic resonance image shows a large well-demarcated inhomogeneous hyperintense lesion in the pancreatic tail (arrow). (C, D) Hemorrhage caused by pancreatic ductal adenocarcinoma in a 66-year-old man. (C) Microscopically, a hemorrhagic area (arrow heads) at the edge of the tumor (black dotted line) (HE×1). (D) Axial T1-weighted fat-saturated magnetic resonance image shows a hypointense (arrow) and inhomogeneous hyperintense (arrowhead) lesion in the pancreatic head."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 2</span></div><div class="figure-caption mb-2"><span class="caption"><p>(A, B) Hemorrhage caused by solid-pseudopapillary neoplasm of the pancreas in an 18-year-old woman. (A) Microscopically, a large well-demarcated lesion with large hemorrhage. (B) Axial T1-weighted fat-saturated magnetic resonance image shows a large well-demarcated inhomogeneous hyperintense lesion in the pancreatic tail (arrow). (C, D) Hemorrhage caused by pancreatic ductal adenocarcinoma in a 66-year-old man. (C) Microscopically, a hemorrhagic area (arrow heads) at the edge of the tumor (black dotted line) (HE×1). (D) Axial T1-weighted fat-saturated magnetic resonance image shows a hypointense (arrow) and inhomogeneous hyperintense (arrowhead) lesion in the pancreatic head.</p></span></div></div></div></div> </section> <section id="j_jtim-2022-0003_s_008"><h2 class="subheading">Cystic degeneration/Variants</h2> <p>Cystic degeneration is found in the SPN, pancreatic undifferentiated carcinoma with osteoclast-like giant cells (UC-OGC), and solid pNET, which are associated with hemorrhage. Cystic pNET might occur as the initial manifestation, which is not related to hemorrhage or necrosis and represents an uncommon variant of pNET.<sup>[<a href="#j_jtim-2022-0003_ref_035" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_035" data-bs-toggle="tooltip" title="35 Paiella S, Marchegiani G, Miotto M, Malpaga A, Impellizzeri H, Montagnini G, et al. Are Cystic Pancreatic Neuroendocrine Tumors an Indolent Entity Results from a Single-Center Surgical Series. Neuroendocrinology 2018;106:234-41.10.1159/000477849Search in Google Scholar&#xA; PubMed&#xA; ">35</a>, <a href="#j_jtim-2022-0003_ref_036" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_036" data-bs-toggle="tooltip" title="36 Singhi AD, Chu LC, Tatsas AD, Shi C, Ellison TA, Fishman EK, et al. Cystic pancreatic neuroendocrine tumors: a clinicopathologic study. Am J Surg Pathol 2012;36:1666-73.10.1097/PAS.0b013e31826a0048Search in Google Scholar&#xA; PubMed&#xA; ">36</a>, <a href="#j_jtim-2022-0003_ref_037" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_037" data-bs-toggle="tooltip" title="37 Koh YX, Chok AY, Zheng HL, Tan CS, Goh BK. A systematic review and meta-analysis of the clinicopathologic characteristics of cystic versus solid pancreatic neuroendocrine neoplasms. Surgery 2014;156:83-96 e82.10.1016/j.surg.2014.03.026Search in Google Scholar">37</a>]</sup></p> <p>Cystic degeneration may also be caused by intratumoral necrosis. Pancreatic adenosquamous carcinoma (PASC), which is a variant of PDAC, shows the central necrosis.<sup>[<a href="#j_jtim-2022-0003_ref_038" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_038" data-bs-toggle="tooltip" title="38 Borazanci E, Millis SZ, Korn R, Han H, Whatcott CJ, Gatalica Z, et al. Adenosquamous carcinoma of the pancreas: Molecular characterization of 23 patients along with a literature review. World J Gastrointest Oncol 2015;7:132-40.10.4251/wjgo.v7.i9.132Search in Google Scholar">38</a>,<a href="#j_jtim-2022-0003_ref_039" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_039" data-bs-toggle="tooltip" title="39 Schawkat K, Tsai LL, Jaramillo-Cardoso A, Paez SN, Moser JA, Decicco C, et al. Use of ring-enhancement and focal necrosis to differentiate pancreatic adenosquamous carcinoma from pancreatic ductal adenocarcinoma on CT and MRI. Clin Imaging 2021;73:134-8.10.1016/j.clinimag.2020.11.041Search in Google Scholar">39</a>]</sup></p> <p>PASC is composed of two distinct components of adenocarcinoma and squamous carcinoma in which the squamous component should be at least 30%<sup>[<a href="#j_jtim-2022-0003_ref_040" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_040" data-bs-toggle="tooltip" title="40 The International Agency for Research on Cancer. WHO classification of tumors of the digestive system. Lyon: International Agency for Research on Cancer (IARC) 2010.Search in Google Scholar">40</a>]</sup>; its imaging characteristics are determined by the proportions and distributions of both components. Most PASCs consist of cells arranged in solid nests and are prone to degeneration, necrosis, and, consequently, cystic lesions due to the lack of blood supply in the central region of the solid nests.<sup>[<a href="#j_jtim-2022-0003_ref_041" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_041" data-bs-toggle="tooltip" title="41 Kosmahl M, Pauser U, Anlauf M, Kloppel G. Pancreatic ductal adenocarcinomas with cystic features: neither rare nor uniform. Mod Pathol 2005;18:1157-64.10.1038/modpathol.3800446Search in Google Scholar">41</a>]</sup> Cystic degeneration exhibits low attenuation on CT scans, hypointense signals on T1WI, and hyperintense signals on T2WI (<a href="#j_jtim-2022-0003_fig_003" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_003">Figure 3</a>).<sup>[<a href="#j_jtim-2022-0003_ref_042" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_042" data-bs-toggle="tooltip" title="42 Imaoka H, Shimizu Y, Mizuno N, Hara K, Hijioka S, Tajika M, et al. Ring-enhancement pattern on contrast-enhanced CT predicts adenosquamous carcinoma of the pancreas: a matched case-control study. Pancreatology 2014;14:221-6.10.1016/j.pan.2014.02.005Search in Google Scholar">42</a>]</sup></p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_003"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_003.jpg" alt="Figure 3 Cystic degeneration caused by pancreatic adenosquamous carcinoma. (A) The tumor with central necrosis (arrowheads) (HE×1). (B) Axial T2-weighted magnetic resonance image shows a round, ill-defined, mild, hypointense mass with central hyperintense necrosis (arrow)."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 3</span></div><div class="figure-caption mb-2"><span class="caption"><p>Cystic degeneration caused by pancreatic adenosquamous carcinoma. (A) The tumor with central necrosis (arrowheads) (HE×1). (B) Axial T2-weighted magnetic resonance image shows a round, ill-defined, mild, hypointense mass with central hyperintense necrosis (arrow).</p></span></div></div></div></div> </section> <section id="j_jtim-2022-0003_s_009"><h2 class="subheading">Fibrosis</h2> <p>The formation of fibers is an important step in tissue repair in the human body and is significant in the reconstruction of tissue structures and functions. Any deviation that develops during the physiological process may lead to abnormal or pathological fibrosis that will seriously affect relevant organs and tissues. There are two types of pancreatic lesions, CP and PDAC, with extraordinarily significant fibrosis as their histological characteristic. Pancreatic stellate cells (PSCs) are distributed in pancreatic interlobular spaces, accounting for 4% of pancreatic tissues. When PSCs are activated, collagen deposition occurs, leading to fibrosis of the organ.<sup>[<a href="#j_jtim-2022-0003_ref_043" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_043" data-bs-toggle="tooltip" title="43 Li ZS, Liao Z, Chen JM, Férec C. Chronic Pancreatitis-From Basic Research to Clinical Treatment. Shanghai: Springer; 2017.10.1007/978-981-10-4515-8Search in Google Scholar">43</a>]</sup></p> <p>The histopathological components of fibers include fibroblasts and fibrocytes, collagen fibers, and inflammatory cells (mainly lymphocytes and histiocytes). Based on the proportions of the above three components, the fibers can be categorized into cell-rich, intermediate, and fiber-rich stroma.</p> <p>In the early stages of CP, fibrosis is rich in cellular and shows a flaky, mainly interlobular distribution.<sup>[<a href="#j_jtim-2022-0003_ref_034" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_034" data-bs-toggle="tooltip" title="34 Campbell F, Verbeke CS. Pathology of the Pancreas. London: Springer 2013.10.1007/978-1-4471-2449-8Search in Google Scholar">34</a>,<a href="#j_jtim-2022-0003_ref_044" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_044" data-bs-toggle="tooltip" title="44 Conwell DL, Lee LS, Yadav D, Longnecker DS, Miller FH, Mortele KJ, et al. American Pancreatic Association Practice Guidelines in Chronic Pancreatitis: evidence-based report on diagnostic guidelines. Pancreas 2014;43:1143-62.10.1097/MPA.0000000000000237Search in Google Scholar">44</a>]</sup> As the disease continues to advance, fibrosis extends with and between atrophic lobules and becomes confluent, forming extensive sheets of fibrosis and scar tissue with few cellularities and abundant collagen content.<sup>[<a href="#j_jtim-2022-0003_ref_044" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_044" data-bs-toggle="tooltip" title="44 Conwell DL, Lee LS, Yadav D, Longnecker DS, Miller FH, Mortele KJ, et al. American Pancreatic Association Practice Guidelines in Chronic Pancreatitis: evidence-based report on diagnostic guidelines. Pancreas 2014;43:1143-62.10.1097/MPA.0000000000000237Search in Google Scholar">44</a>, <a href="#j_jtim-2022-0003_ref_045" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_045" data-bs-toggle="tooltip" title="45 Kleeff J, Whitcomb DC, Shimosegawa T, Esposito I, Lerch MM, Gress T, et al. Chronic pancreatitis. Nat Rev Dis Primers 2017;3:17060.10.1038/nrdp.2017.60Search in Google Scholar">45</a>, <a href="#j_jtim-2022-0003_ref_046" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_046" data-bs-toggle="tooltip" title="46 Majumder S, Chari ST. Chronic pancreatitis. Lancet 2016;387:1957-66.10.1016/S0140-6736(16)00097-0Search in Google Scholar">46</a>]</sup></p> <p>PDAC consists of highly infiltrated neoplastic epithelial tumor cells, which are embedded in a remarkable desmoplastic stroma.<sup>[<a href="#j_jtim-2022-0003_ref_047" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_047" data-bs-toggle="tooltip" title="47 Ho WJ, Jaffee EM, Zheng L. The tumour microenvironment in pancreatic cancer - clinical challenges and opportunities. Nat Rev Clin Oncol 2020;17:527-40.10.1038/s41571-020-0363-5Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">47</a>]</sup> The desmoplastic stroma is composed of fibroblasts, collagen fibers, and a scattering of inflammatory cells. The tumor stroma can vary from cellular rich with more densely packed tumor glands to less cellular and abundant collagen.<sup>[<a href="#j_jtim-2022-0003_ref_034" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_034" data-bs-toggle="tooltip" title="34 Campbell F, Verbeke CS. Pathology of the Pancreas. London: Springer 2013.10.1007/978-1-4471-2449-8Search in Google Scholar">34</a>]</sup></p> <p>Fibrosis shows low attenuation on CT, hypointense signals on MRI T1WI, and slightly hyperintense or iso-hyperintense signals on T2WI.</p> </section> <section id="j_jtim-2022-0003_s_010"><h2 class="subheading">Pancreatic duct alterations</h2> <p>Pancreatic lesions can be categorized into lesions without ductal communication (pancreatic extraductal lesions) and lesions with ductal communication (partially intraductal pancreatic lesions). Pancreatic lesions can show the different patterns of pancreatic duct dilatation: upstream, downstream, and diffuse. The relationship between most pancreatic masses and pancreatic ducts can be confirmed via magnetic resonance cholangiopancreatography (MRCP) or multiplanar reformation (MPR) along the main pancreatic duct.</p> <p>Parenchymal fibrosis and calculi result in pancreatic changes in CP. The spectrum of changes in the pancreatic duct is wide and may include stricture, dilatation, stenosis of intraductal calculi, and occasional side-branch duct dilatation (<a href="#j_jtim-2022-0003_fig_004" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_004">Figure 4A, B)</a>.<sup>[<a href="#j_jtim-2022-0003_ref_045" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_045" data-bs-toggle="tooltip" title="45 Kleeff J, Whitcomb DC, Shimosegawa T, Esposito I, Lerch MM, Gress T, et al. Chronic pancreatitis. Nat Rev Dis Primers 2017;3:17060.10.1038/nrdp.2017.60Search in Google Scholar">45</a>]</sup></p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_004"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_004.jpg" alt="Figure 4 (A, B) Pancreatic duct alteration caused by severe chronic pancreatitis in a 58-year-old man. (A) Pancreatic stones from the specimen. (B) Axial unenhanced computed tomography image shows a dilated pancreatic duct, multiple calcifications throughout the pancreas, and parenchymal atrophy. (C, D) Pancreatic duct alteration caused by G2 nonfunctional pancreatic neuroendocrine tumor in a 72-year-old man. (C) Surgical specimen (distal pancreatectomy): a yellowish lesion (red dotted line) of pancreatic body with upstream duct dilation (black arrows). (D) Axial portal vein phase computed tomography image shows a hypervascular mass (arrow) in the pancreatic body with significantly dilated upstream main pancreatic ducts (arrow head). (E, F) Double-duct sign caused by a pancreatic ductal adenocarcinoma in a 68-year-old man. (E) Surgical specimen (pancreaticoduodenectomy): a hard, whitish lesion (arrow head) with irregular faint margins presenting infiltrative growth pattern, with involvement of the Wirsung duct and common bile duct, both upstream-dilated (double-duct sign). (F) 2D magnetic resonance cholangiopancreatography image shows significant dilation of the biliary tree and Wirsung duct (double-duct sign). (G, H) Pancreatic duct alteration caused by main-duct intraductal papillary mucinous neoplasm in a 64-year-old woman. (G) Surgical specimen (total pancreatectomy): main pancreatic duct significantly and diffusely dilated and filled with mucoid material. (H) Axial arterial phase computed tomography image shows the diffuse dilation of the main pancreatic duct (arrow)."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 4</span></div><div class="figure-caption mb-2"><span class="caption"><p>(A, B) Pancreatic duct alteration caused by severe chronic pancreatitis in a 58-year-old man. (A) Pancreatic stones from the specimen. (B) Axial unenhanced computed tomography image shows a dilated pancreatic duct, multiple calcifications throughout the pancreas, and parenchymal atrophy. (C, D) Pancreatic duct alteration caused by G2 nonfunctional pancreatic neuroendocrine tumor in a 72-year-old man. (C) Surgical specimen (distal pancreatectomy): a yellowish lesion (red dotted line) of pancreatic body with upstream duct dilation (black arrows). (D) Axial portal vein phase computed tomography image shows a hypervascular mass (arrow) in the pancreatic body with significantly dilated upstream main pancreatic ducts (arrow head). (E, F) Double-duct sign caused by a pancreatic ductal adenocarcinoma in a 68-year-old man. (E) Surgical specimen (pancreaticoduodenectomy): a hard, whitish lesion (arrow head) with irregular faint margins presenting infiltrative growth pattern, with involvement of the Wirsung duct and common bile duct, both upstream-dilated (double-duct sign). (F) 2D magnetic resonance cholangiopancreatography image shows significant dilation of the biliary tree and Wirsung duct (double-duct sign). (G, H) Pancreatic duct alteration caused by main-duct intraductal papillary mucinous neoplasm in a 64-year-old woman. (G) Surgical specimen (total pancreatectomy): main pancreatic duct significantly and diffusely dilated and filled with mucoid material. (H) Axial arterial phase computed tomography image shows the diffuse dilation of the main pancreatic duct (arrow).</p></span></div></div></div></div> <p>Autoimmune pancreatitis (AIP) is characterized by periductal lymphoplasmacytic inflammation, phlebitis, and fibrosis.<sup>[<a href="#j_jtim-2022-0003_ref_048" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_048" data-bs-toggle="tooltip" title="48 Deshpande V, Zen Y, Chan JK, Yi EE, Sato Y, Yoshino T, et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol 2012;25:1181-92.10.1038/modpathol.2012.72Search in Google Scholar&#xA; PubMed&#xA; ">48</a>]</sup> The medium-sized ducts are often involved by the periductal inflammation. Segmental or diffuse stenosis of the main pancreatic duct is the characteristic finding in endoscopic retrograde cholangiopancreatography.<sup>[<a href="#j_jtim-2022-0003_ref_049" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_049" data-bs-toggle="tooltip" title="49 Sahani DV, Kalva SP, Farrell J, Maher MM, Saini S, Mueller PR, et al. Autoimmune pancreatitis: imaging features. Radiology 2004;233:345-52.10.1148/radiol.2332031436Search in Google Scholar&#xA; PubMed&#xA; ">49</a>,<a href="#j_jtim-2022-0003_ref_050" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_050" data-bs-toggle="tooltip" title="50 Horiuchi A, Kawa S, Hamano H, Hayama M, Ota H, Kiyosawa K. ERCP features in 27 patients with autoimmune pancreatitis. Gastrointest Endosc 2002;55:494-9.10.1067/mge.2002.12265Search in Google Scholar">50</a>]</sup> CT and MRI often detect mild pancreatic ductal dilation and the upstream narrowed segment.<sup>[<a href="#j_jtim-2022-0003_ref_051" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_051" data-bs-toggle="tooltip" title="51 Dong Y, D’Onofrio M, Hocke M, Jenssen C, Potthoff A, Atkinson N, et al. Autoimmune pancreatitis: Imaging features. Endosc Ultrasound 2018;7:196-203.10.4103/eus.eus_23_17Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">51</a>,<a href="#j_jtim-2022-0003_ref_052" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_052" data-bs-toggle="tooltip" title="52 Sureka B, Bansal K. Autoimmune Pancreatitis: Additional Key Imaging Features. AJR Am J Roentgenol 2016;207:W4.10.2214/AJR.16.16164Search in Google Scholar&#xA; PubMed&#xA; ">52</a>]</sup> Low-grade malignant tumors (such as pNET, SPN, or SCN) often compress the lesion areas on pancreatic ducts, resulting in stenosis or abrupt cutoff of pancreatic ducts, followed by upstream pancreatic duct dilation. However, the degree of upstream pancreatic duct dilation is usually milder than that in PDAC due to the relatively soft nature and slow growth of the mass (<a href="#j_jtim-2022-0003_fig_004" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_004">Figure 4C, D)</a>.</p> <p>PDAC can easily compress or invade the ducts and cause variable degrees of stenosis, ultimately resulting in complete stenosis and upstream pancreatic duct dilation. A minute carcinoma may only manifest with abdominal pain and significant dilatation of the main pancreatic duct (MPD). Therefore, careful observation of minor changes in the pancreatic duct may help detect small pancreatic tumors. The typical “double-duct sign” occurs when a carcinoma located in the pancreatic head compresses or invades the pancreatic duct and the common bile duct, combining “soft-rattan” dilation of the common bile duct (<a href="#j_jtim-2022-0003_fig_004" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_004">Figure 4E, F)</a>.</p> <p>Lesions with ductal communication mainly include IPMN, pancreatic intraductal tubulopapillary neoplasm (ITPN), and PPC; pNET rarely develops in pancreatic ducts. The communication between the main pancreatic duct and the cystic lesion is a vital feature at diagnosis.</p> <p>Based on IPMN imaging<sup>[<a href="#j_jtim-2022-0003_ref_053" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_053" data-bs-toggle="tooltip" title="53 Tanaka M, Fernandez-del Castillo C, Adsay V, Chari S, Falconi M, Jang JY, et al. International consensus guidelines 2012 for the management of IPMN and MCN of the pancreas. Pancreatology 2012;12:183-97.10.1016/j.pan.2012.04.004Search in Google Scholar&#xA; PubMed&#xA; ">53</a>]</sup> and gross pathological findings, the location of ductal involvement can be categorized as in the main duct, branch duct, or a mixture of both; each category accounts for approximately one third of resected IPMNs.<sup>[<a href="#j_jtim-2022-0003_ref_054" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_054" data-bs-toggle="tooltip" title="54 Crippa S, Fernandez-Del Castillo C, Salvia R, Finkelstein D, Bassi C, Dominguez I, et al. Mucin-producing neoplasms of the pancreas: an analysis of distinguishing clinical and epidemiologic characteristics. Clin Gastroenterol Hepatol 2010;8:213-9.10.1016/j.cgh.2009.10.001Search in Google Scholar&#xA; PubMed&#xA; &#xA; PubMed Central&#xA; ">54</a>,<a href="#j_jtim-2022-0003_ref_055" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_055" data-bs-toggle="tooltip" title="55 Nara S, Onaya H, Hiraoka N, Shimada K, Sano T, Sakamoto Y, et al. Preoperative evaluation of invasive and noninvasive intraductal papillary-mucinous neoplasms of the pancreas: clinical, radiological, and pathological analysis of 123 cases. Pancreas 2009;38:8-16.10.1097/MPA.0b013e318181b90dSearch in Google Scholar&#xA; PubMed&#xA; ">55</a>]</sup> The imaging characteristics of IPMN lie on the location of the tumors. The main-duct type appears as diffuse or segmental duct dilation (<a href="#j_jtim-2022-0003_fig_004" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_004">Figure 4G, H)</a>.<sup>[<a href="#j_jtim-2022-0003_ref_056" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_056" data-bs-toggle="tooltip" title="56 Lim JH, Lee G, Oh YL. Radiologic spectrum of intraductal papillary mucinous tumor of the pancreas. Radiographics 2001;21:323-37; discussion 337-40.10.1148/radiographics.21.2.g01mr01323Search in Google Scholar&#xA; PubMed&#xA; ">56</a>,<a href="#j_jtim-2022-0003_ref_057" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_057" data-bs-toggle="tooltip" title="57 Sakorafas GH, Smyrniotis V, Reid-Lombardo KM, Sarr MG. Primary pancreatic cystic neoplasms revisited. Part III. Intraductal papillary mucinous neoplasms. Surg Oncol 2011;20:e109-18.10.1016/j.suronc.2011.01.004Search in Google Scholar&#xA; PubMed&#xA; ">57</a>]</sup> The branch-duct type appears as clustered pleomorphic cysts or a unilocular cystic lesion and is often located in the uncinate process.<sup>[<a href="#j_jtim-2022-0003_ref_057" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_057" data-bs-toggle="tooltip" title="57 Sakorafas GH, Smyrniotis V, Reid-Lombardo KM, Sarr MG. Primary pancreatic cystic neoplasms revisited. Part III. Intraductal papillary mucinous neoplasms. Surg Oncol 2011;20:e109-18.10.1016/j.suronc.2011.01.004Search in Google Scholar&#xA; PubMed&#xA; ">57</a>]</sup> ITPN is an extremely rare pancreatic intraductal tumor that produces relatively less mucus. PPCs represent collections of pancreatic juice secondary to duct rupture due to increased pancreatic duct pressure, stenosis, calculi, and occlusion caused by protein plugs.<sup>[<a href="#j_jtim-2022-0003_ref_034" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_034" data-bs-toggle="tooltip" title="34 Campbell F, Verbeke CS. Pathology of the Pancreas. London: Springer 2013.10.1007/978-1-4471-2449-8Search in Google Scholar">34</a>]</sup></p> </section> <section id="j_jtim-2022-0003_s_011"><h2 class="subheading">Microvessel</h2> <p>The arterial supply to the pancreas is derived from branches of superior mesenteric artery and the celiac trunk.<sup>[<a href="#j_jtim-2022-0003_ref_058" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_058" data-bs-toggle="tooltip" title="58 Casillas J, Levi JU, Quiroz AO, Ruiz-Cordero R, Garcia-Buitrago MT, Sleeman D. Multidisciplinary Teaching Atlas of the Pancreas. Berlin: Springer 2016.10.1007/978-3-662-46745-9Search in Google Scholar">58</a>]</sup> Lobular branches emanating from these arterial branches along interlobular connective tissues enter pancreatic lobules and give rise to intralobular arteries that provide blood to exocrine glands. Owing to the highly vascular nature of the pancreas, the normal pancreatic parenchyma demonstrates a homogeneous blush shortly after the arrival of a contrast agent in the abdominal aorta. However, the contrast agent can also wash out in the delayed phase owing to the abundant pancreatic venous drainage network.</p> <p>In mild AP, the edematous pancreas shows that the collections of fibrin and neutrophils may be present in the widened interlobular septa.<sup>[<a href="#j_jtim-2022-0003_ref_034" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_034" data-bs-toggle="tooltip" title="34 Campbell F, Verbeke CS. Pathology of the Pancreas. London: Springer 2013.10.1007/978-1-4471-2449-8Search in Google Scholar">34</a>]</sup> Blood-vessel dilation and congestion are found by microscope. Therefore, edematous pancreatic parenchyma often shows a normal or mildly uneven “slow-in and slow-out” pattern of enhancement postcontrast. In severe AP, any of the tissues and the constituent cells of the pancreas can be involved. Necrosis of the pancreatic parenchyma is the important feature. The necrotic area shows nonenhancement due to the lack of blood supply. Therefore, contrast-enhanced examinations are effective for the detection of necrotic areas.</p> <p>Microscopic examination shows that acinar atrophy, fibrosis, and pancreatic duct changes represent the essential triad of CP.<sup>[<a href="#j_jtim-2022-0003_ref_044" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_044" data-bs-toggle="tooltip" title="44 Conwell DL, Lee LS, Yadav D, Longnecker DS, Miller FH, Mortele KJ, et al. American Pancreatic Association Practice Guidelines in Chronic Pancreatitis: evidence-based report on diagnostic guidelines. Pancreas 2014;43:1143-62.10.1097/MPA.0000000000000237Search in Google Scholar">44</a>, <a href="#j_jtim-2022-0003_ref_045" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_045" data-bs-toggle="tooltip" title="45 Kleeff J, Whitcomb DC, Shimosegawa T, Esposito I, Lerch MM, Gress T, et al. Chronic pancreatitis. Nat Rev Dis Primers 2017;3:17060.10.1038/nrdp.2017.60Search in Google Scholar">45</a>, <a href="#j_jtim-2022-0003_ref_046" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_046" data-bs-toggle="tooltip" title="46 Majumder S, Chari ST. Chronic pancreatitis. Lancet 2016;387:1957-66.10.1016/S0140-6736(16)00097-0Search in Google Scholar">46</a>]</sup> The enhancement characteristics for CP are determined by the proportion and distribution of residual normal pancreatic tissues and fibrosis. The sensitivity of MRI seems to be superior to that of CT, especially for the diagnosis of early-stage CP.<sup>[<a href="#j_jtim-2022-0003_ref_044" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_044" data-bs-toggle="tooltip" title="44 Conwell DL, Lee LS, Yadav D, Longnecker DS, Miller FH, Mortele KJ, et al. American Pancreatic Association Practice Guidelines in Chronic Pancreatitis: evidence-based report on diagnostic guidelines. Pancreas 2014;43:1143-62.10.1097/MPA.0000000000000237Search in Google Scholar">44</a>]</sup> Early-stage CP is characterized by the presence of abundant normal pancreatic tissues and mild fibrosis. It is difficult to detect in unenhanced imaging and only shows minimal delayed postcontrast enhancement. As the disease progresses, CP is characterized by significant fibrosis and atrophic lobules. The pancreatic parenchyma shows significant hypointensity on T1WI and slightly hyperintense or isointense signals on T2WI with significant delayed postcontrast enhancement.</p> <p>The stroma in pNET typically consists of a delicate fibrovascular network. Most pNETs are more significantly enhanced than normal pancreatic tissues (<a href="#j_jtim-2022-0003_fig_005" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_005">Figure 5A, B)</a> in the arterial phase or in the portal venous phase. With a small number of poorly differentiated tumor cells, abundant stroma, and reduced fibrovascular network, pNET can be easily misdiagnosed as PC, as it may also show hypoenhancement or delayed minimal enhancement on imaging.</p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_005"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_005.jpg" alt="Figure 5 (A, B) Hypervascular G2 nonfunctional pancreatic neuroendocrine tumor in a 58-year-old woman. (A) High intralesional vascular network is shown with CD34 immunohistochemical staining (IHC×100). (B) Axial arterial phase computed tomography image shows inhomogeneous hypervascularity (arrows). (C–E) Enhancement feature of the pancreatic ductal adenocarcinoma in a 58-year-old man. (C) The mass (black arrowhead) with a few residual normal pancreatic tissues at its periphery (green lines) is shown with CD34 immunohistochemical staining (IHC×1). (D) Axial unenhanced computed tomography image shows a solid, round, and distinct border and a low-attenuation mass in the pancreatic head. (E) Axial computed tomography image in delayed phase shows the mass with mild progressive enhancement, especially at its periphery."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 5</span></div><div class="figure-caption mb-2"><span class="caption"><p>(A, B) Hypervascular G2 nonfunctional pancreatic neuroendocrine tumor in a 58-year-old woman. (A) High intralesional vascular network is shown with CD34 immunohistochemical staining (IHC×100). (B) Axial arterial phase computed tomography image shows inhomogeneous hypervascularity (arrows). (C–E) Enhancement feature of the pancreatic ductal adenocarcinoma in a 58-year-old man. (C) The mass (black arrowhead) with a few residual normal pancreatic tissues at its periphery (green lines) is shown with CD34 immunohistochemical staining (IHC×1). (D) Axial unenhanced computed tomography image shows a solid, round, and distinct border and a low-attenuation mass in the pancreatic head. (E) Axial computed tomography image in delayed phase shows the mass with mild progressive enhancement, especially at its periphery.</p></span></div></div></div></div> <p>Despite the presence of abundant thin-walled blood vessels in the stroma of the SPN that usually exhibit hyaline degeneration and collagenation, the contrast agent can only enter the tumor tissues slowly via thick-walled blood vessels. The mass shows hypoenhancement in the arterial phase and delayed progressive enhancement; the degree of enhancement is lower than that of its surrounding normal pancreatic parenchyma.</p> <p>Previous research has shown that prognostic significance is better assessed by quantification of the total vascular area (TVA) and the branching pattern of microvessels than the microussel density (MVD) for colorectal carcinoma patients.<sup>[<a href="#j_jtim-2022-0003_ref_059" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_059" data-bs-toggle="tooltip" title="59 Pavlopoulos PM, Konstantinidou AE, Agapitos E, Kavantzas N, Nikolopoulou P, Davaris P. A morphometric study of neovascularization in colorectal carcinoma. Cancer 1998;83:2067-75.10.1002/(SICI)1097-0142(19981115)83:10&lt;2067::AID-CNCR4&gt;3.0.CO;2-QSearch in Google Scholar">59</a>]</sup> PDAC is microscopically composed of tumor cells, stoma, and residual atrophic acinus. The degree of enhancement of PDAC is determined by the MVD and TVA in the tumor.<sup>[<a href="#j_jtim-2022-0003_ref_060" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_060" data-bs-toggle="tooltip" title="60 Giannopoulos G, Kavantzas N, Parasi A, Tiniakos D, Peros G, Tzanakis N, et al. Morphometric microvascular characteristics in the prognosis of pancreatic and ampullary carcinoma. Pancreas 2007;35:47-52.10.1097/mpa.0b013e31804bfbabSearch in Google Scholar">60</a>]</sup> PDACs have varying proportions of tumor cells and stroma, as well as varying degrees of inflammation. Moreover, there may or may not be residual normal pancreatic tissues in the tumors with varying extents and distributions. These differential microscopic observations determine the enhancement pattern of the tumor (<a href="#j_jtim-2022-0003_fig_005" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_005">Figure 5C–E)</a>.</p> <p>The pathological basis of enhanced SCN and MCN is the network of small capillary-sized vessels immediately beneath the epithelium. After contrast administration, the vascularization of internal septa is clear, and when extremely microcystic, the SCN may even mimic a solid hypervascular lesion.<sup>[<a href="#j_jtim-2022-0003_ref_061" class="link link-bibr" data-bs-target="j_jtim-2022-0003_ref_061" data-bs-toggle="tooltip" title="61 Kim SY, Park SH, Hong N, Kim JH, Hong SM. Primary solid pancreatic tumors: recent imaging findings updates with pathology correlation. Abdom Imaging 2013;38:1091-105.10.1007/s00261-013-0004-xSearch in Google Scholar">61</a>]</sup> Currently, MRI T2WI and MRCP help diagnose the hyperintense cyst fluid (<a href="#j_jtim-2022-0003_fig_006" class="link link-fig" data-bs-target="j_jtim-2022-0003_fig_006">Figure 6</a>). Additionally, the enhanced solid components of pancreatic cystic masses, such as mural nodules in the IPMN and MCN, reveal the mass’s relationship with the tumor microvessel.</p> <div class="figure-wrapper" id="j_jtim-2022-0003_fig_006"><div class="figure w-100"><div class="graphic"><img loading="lazy" src="/document/doi/10.2478/jtim-2022-0003/asset/graphic/j_jtim-2022-0003_fig_006.jpg" alt="Figure 6 Enhancement feature of the serous cystic neoplasm of the pancreas in a 45-year-old woman. (A) Microscopic examination of the tumor shows the network of small capillary-sized vessels beneath the epithelium with CD34 immunohistochemical staining (IHC×40). (B) Axial T2-weighted image shows lobulated, distinct borders and a hyperintense mass (arrow). (C) T1-weighted magnetic resonance image in the arterial phase shows the mass is hypervascular (arrowhead)."></img></div><div class="figure-description mb-3"><div class="figure-label h3"><span class="label">Figure 6</span></div><div class="figure-caption mb-2"><span class="caption"><p>Enhancement feature of the serous cystic neoplasm of the pancreas in a 45-year-old woman. (A) Microscopic examination of the tumor shows the network of small capillary-sized vessels beneath the epithelium with CD34 immunohistochemical staining (IHC×40). (B) Axial T2-weighted image shows lobulated, distinct borders and a hyperintense mass (arrow). (C) T1-weighted magnetic resonance image in the arterial phase shows the mass is hypervascular (arrowhead).</p></span></div></div></div></div> </section> <section id="j_jtim-2022-0003_s_012"><h2 class="subheading">Conclusion</h2> <p>Although pancreatic diseases are a widely known and easily recognizable condition in its typical presentation, there are some less well-known forms that may be challenging and/or demand special attention on imaging. However, diagnosis of pancreatic diseases can be challenging due to numerous pitfalls associated with image acquisition and interpretation, including technical factors, imaging features, and cognitive errors. Accurate diagnosis requires familiarity with these pitfalls and deep understanding of pathology, as these can be minimized using systematic strategies.</p> <p>To overcome the current limitations of imaging, researchers have developed radiomics. 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In the future, the diagnosis of pancreatic diseases will enter an era of precision and individuation.</p> </section> </div><section class="authorNotes"><hr></hr> <div class="correspondingAuthor">Prof. Jianping Lu, MD, PhD, Department of Radiology, Changhai Hospital, The Navy Military Medical University, 168 Changhai Road, Shanghai 200433, China</div> <hr></hr></section><div class="contrib-group"></div><div class="back"> <ol class="footnote-group" id=""> <li class="footnote footnote-noLabel" id="j_jtim-2022-0003_fn_001" fn-type="conflict"> <p><strong>Conflict of Interest</strong></p> <p>The authors have no conflicts of interest to disclose.</p> </li> <li class="footnote footnote-noLabel" id="j_jtim-2022-0003_fn_101" fn-type="other"> <p><strong>Source of Funding</strong></p> <p>This work was supported in part by the National Science Foundation for Scientists of China (No. 81871352, 82171915, and 82171930), Clinical Research Plan of SHDC (No. SHDC2020CR4073), 234 Platform Discipline Consolidation Foundation Project (No. 2019YPT001, 2020YPT001), and The Natural Science Foundation of Shanghai Science and Technology Innovation Action Plan (No. 21ZR1478500, 21Y11910300).</p> </li> <li class="footnote footnote-noLabel" id="j_jtim-2022-0003_fn_111" fn-type="other"> <p><strong>Permissions</strong></p> <p>All figures in this article are reprinted with permission from the authors' own publication (Jianping Lu. 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"Basic pancreatic lesions: Radiologic-pathologic correlation" <i>Journal of Translational Internal Medicine</i>, vol. 10, no. 1, 2022, pp. 18-27. <a href='https://doi.org/10.2478/jtim-2022-0003'>https://doi.org/10.2478/jtim-2022-0003</a></div> <div class="tab-pane fade " id="APA" role="tabpanel" aria-labelledby="APA-tab">Bian, Y., Jiang, H., Zheng, J., Shao, C. & Lu, J. (2022). Basic pancreatic lesions: Radiologic-pathologic correlation. <i>Journal of Translational Internal Medicine</i>, <i>10</i>(1), 18-27. <a href='https://doi.org/10.2478/jtim-2022-0003'>https://doi.org/10.2478/jtim-2022-0003</a></div> <div class="tab-pane fade " id="Harvard" role="tabpanel" aria-labelledby="Harvard-tab">Bian, Y., Jiang, H., Zheng, J., Shao, C. and Lu, J. (2022) Basic pancreatic lesions: Radiologic-pathologic correlation. Journal of Translational Internal Medicine, Vol. 10 (Issue 1), pp. 18-27. <a href='https://doi.org/10.2478/jtim-2022-0003'>https://doi.org/10.2478/jtim-2022-0003</a></div> <div class="tab-pane fade " id="Chicago" role="tabpanel" aria-labelledby="Chicago-tab">Bian, Yun, Jiang, Hui, Zheng, Jianming, Shao, Chengwei and Lu, Jianping. "Basic pancreatic lesions: Radiologic-pathologic correlation" <i>Journal of Translational Internal Medicine</i> 10, no. 1 (2022): 18-27. <a href='https://doi.org/10.2478/jtim-2022-0003'>https://doi.org/10.2478/jtim-2022-0003</a></div> <div class="tab-pane fade " id="Vancouver" role="tabpanel" aria-labelledby="Vancouver-tab">Bian Y, Jiang H, Zheng J, Shao C, Lu J. 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