Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature
Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acin...
Gespeichert in:
| Veröffentlicht in: | International journal of surgical pathology 2022-08, Vol.30 (5), p.528-538 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 538 |
|---|---|
| container_issue | 5 |
| container_start_page | 528 |
| container_title | International journal of surgical pathology |
| container_volume | 30 |
| creator | Paseiro-Crespo, Gloria García-Nebreda, María Roldán Cortés, David De la Peña Navarro, Itziar Álvaro Cifuentes, Edurne Marqués Medina, Elia Abad-Motos, Ane |
| description | Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acinar carcinoma of the stomach coexisting with a large cell B lymphoma synchronously, and a literature review of gastric carcinomas with pancreatic cell differentiation. At present there is a preoperative underdiagnosis of these tumours that could be minimized by including this entity in the differential diagnosis of gastric cancer and by performing immunohistochemical analysis with neuroendocrine markers and exocrine pancreatic enzymes. |
| doi_str_mv | 10.1177/10668969211065763 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2622478665</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_10668969211065763</sage_id><sourcerecordid>2622478665</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-b93b26740c476949ffadc6cf0e24663b8c561dc8dd381a32edfdff691d55a06a3</originalsourceid><addsrcrecordid>eNp1kdtOGzEQhq2qqFDoA_SmstQbbhZ82J3d7V2U0oIUiQjo9WriAzFKdoPtLcoj8NYdFGilIq48I3_z_3Ng7LMUJ1LW9akUAE0LrZIUVTXod-xAtqUoVAnVe4rpv3gC9tnHlO6EEAqU_MD2dSWgUUofsMd5DGuMWz4fo-Nz7E10mIPhxc124_jEhB4jn7rVik8xUjaskQ-e56Xj15kSs_zGJ_wKqfqszyFv-UPIS478e_A-mHGVKcLbfkghcewtv3K_g3t40ZiF7CJmMj9iex5XyX16fg_Zrx9nN9PzYnb582I6mRVGQ5OLRasXCupSmLKGtmy9R2vAeOFoaNCLxlQgrWms1Y1ErZz11ntopa0qFID6kB3vdDdxuB9dyt06JEMDYu-GMXW0IlXWDUBF6Nf_0LthjD11R1RTabIvJVFyR5k4pBSd7za7nXZSdE936l7diWq-PCuPi7WzfyteDkPAyQ5IeOv-2b6t-AfiLpos</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2685394941</pqid></control><display><type>article</type><title>Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature</title><source>Access via SAGE</source><source>MEDLINE</source><creator>Paseiro-Crespo, Gloria ; García-Nebreda, María ; Roldán Cortés, David ; De la Peña Navarro, Itziar ; Álvaro Cifuentes, Edurne ; Marqués Medina, Elia ; Abad-Motos, Ane</creator><creatorcontrib>Paseiro-Crespo, Gloria ; García-Nebreda, María ; Roldán Cortés, David ; De la Peña Navarro, Itziar ; Álvaro Cifuentes, Edurne ; Marqués Medina, Elia ; Abad-Motos, Ane</creatorcontrib><description>Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acinar carcinoma of the stomach coexisting with a large cell B lymphoma synchronously, and a literature review of gastric carcinomas with pancreatic cell differentiation. At present there is a preoperative underdiagnosis of these tumours that could be minimized by including this entity in the differential diagnosis of gastric cancer and by performing immunohistochemical analysis with neuroendocrine markers and exocrine pancreatic enzymes.</description><identifier>ISSN: 1066-8969</identifier><identifier>EISSN: 1940-2465</identifier><identifier>DOI: 10.1177/10668969211065763</identifier><identifier>PMID: 35068223</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Biopsy ; Carcinoma, Acinar Cell - diagnosis ; Carcinoma, Acinar Cell - pathology ; Female ; Gastric cancer ; Humans ; Immunohistochemistry ; Middle Aged ; Neuroendocrine tumors ; Pancreas ; Pancreatic Neoplasms ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - pathology ; Stomach Neoplasms - diagnosis ; Stomach Neoplasms - pathology</subject><ispartof>International journal of surgical pathology, 2022-08, Vol.30 (5), p.528-538</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-b93b26740c476949ffadc6cf0e24663b8c561dc8dd381a32edfdff691d55a06a3</citedby><cites>FETCH-LOGICAL-c368t-b93b26740c476949ffadc6cf0e24663b8c561dc8dd381a32edfdff691d55a06a3</cites><orcidid>0000-0002-9118-9392 ; 0000-0003-2555-0212</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/10668969211065763$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/10668969211065763$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35068223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Paseiro-Crespo, Gloria</creatorcontrib><creatorcontrib>García-Nebreda, María</creatorcontrib><creatorcontrib>Roldán Cortés, David</creatorcontrib><creatorcontrib>De la Peña Navarro, Itziar</creatorcontrib><creatorcontrib>Álvaro Cifuentes, Edurne</creatorcontrib><creatorcontrib>Marqués Medina, Elia</creatorcontrib><creatorcontrib>Abad-Motos, Ane</creatorcontrib><title>Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature</title><title>International journal of surgical pathology</title><addtitle>Int J Surg Pathol</addtitle><description>Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acinar carcinoma of the stomach coexisting with a large cell B lymphoma synchronously, and a literature review of gastric carcinomas with pancreatic cell differentiation. At present there is a preoperative underdiagnosis of these tumours that could be minimized by including this entity in the differential diagnosis of gastric cancer and by performing immunohistochemical analysis with neuroendocrine markers and exocrine pancreatic enzymes.</description><subject>Biopsy</subject><subject>Carcinoma, Acinar Cell - diagnosis</subject><subject>Carcinoma, Acinar Cell - pathology</subject><subject>Female</subject><subject>Gastric cancer</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Middle Aged</subject><subject>Neuroendocrine tumors</subject><subject>Pancreas</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Stomach Neoplasms - diagnosis</subject><subject>Stomach Neoplasms - pathology</subject><issn>1066-8969</issn><issn>1940-2465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kdtOGzEQhq2qqFDoA_SmstQbbhZ82J3d7V2U0oIUiQjo9WriAzFKdoPtLcoj8NYdFGilIq48I3_z_3Ng7LMUJ1LW9akUAE0LrZIUVTXod-xAtqUoVAnVe4rpv3gC9tnHlO6EEAqU_MD2dSWgUUofsMd5DGuMWz4fo-Nz7E10mIPhxc124_jEhB4jn7rVik8xUjaskQ-e56Xj15kSs_zGJ_wKqfqszyFv-UPIS478e_A-mHGVKcLbfkghcewtv3K_g3t40ZiF7CJmMj9iex5XyX16fg_Zrx9nN9PzYnb582I6mRVGQ5OLRasXCupSmLKGtmy9R2vAeOFoaNCLxlQgrWms1Y1ErZz11ntopa0qFID6kB3vdDdxuB9dyt06JEMDYu-GMXW0IlXWDUBF6Nf_0LthjD11R1RTabIvJVFyR5k4pBSd7za7nXZSdE936l7diWq-PCuPi7WzfyteDkPAyQ5IeOv-2b6t-AfiLpos</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Paseiro-Crespo, Gloria</creator><creator>García-Nebreda, María</creator><creator>Roldán Cortés, David</creator><creator>De la Peña Navarro, Itziar</creator><creator>Álvaro Cifuentes, Edurne</creator><creator>Marqués Medina, Elia</creator><creator>Abad-Motos, Ane</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9118-9392</orcidid><orcidid>https://orcid.org/0000-0003-2555-0212</orcidid></search><sort><creationdate>20220801</creationdate><title>Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature</title><author>Paseiro-Crespo, Gloria ; García-Nebreda, María ; Roldán Cortés, David ; De la Peña Navarro, Itziar ; Álvaro Cifuentes, Edurne ; Marqués Medina, Elia ; Abad-Motos, Ane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-b93b26740c476949ffadc6cf0e24663b8c561dc8dd381a32edfdff691d55a06a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biopsy</topic><topic>Carcinoma, Acinar Cell - diagnosis</topic><topic>Carcinoma, Acinar Cell - pathology</topic><topic>Female</topic><topic>Gastric cancer</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Middle Aged</topic><topic>Neuroendocrine tumors</topic><topic>Pancreas</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Stomach Neoplasms - diagnosis</topic><topic>Stomach Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paseiro-Crespo, Gloria</creatorcontrib><creatorcontrib>García-Nebreda, María</creatorcontrib><creatorcontrib>Roldán Cortés, David</creatorcontrib><creatorcontrib>De la Peña Navarro, Itziar</creatorcontrib><creatorcontrib>Álvaro Cifuentes, Edurne</creatorcontrib><creatorcontrib>Marqués Medina, Elia</creatorcontrib><creatorcontrib>Abad-Motos, Ane</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of surgical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paseiro-Crespo, Gloria</au><au>García-Nebreda, María</au><au>Roldán Cortés, David</au><au>De la Peña Navarro, Itziar</au><au>Álvaro Cifuentes, Edurne</au><au>Marqués Medina, Elia</au><au>Abad-Motos, Ane</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature</atitle><jtitle>International journal of surgical pathology</jtitle><addtitle>Int J Surg Pathol</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>30</volume><issue>5</issue><spage>528</spage><epage>538</epage><pages>528-538</pages><issn>1066-8969</issn><eissn>1940-2465</eissn><abstract>Acinar cell carcinoma is an uncommon tumour, representing only 1% to 2% of all exocrine pancreatic tumours. Pancreatic-type acinar cell carcinoma can occur in other organs, including the stomach, but it is extraordinarily rare. We report a case of a 51-year-old woman with a pancreatic-type pure acinar carcinoma of the stomach coexisting with a large cell B lymphoma synchronously, and a literature review of gastric carcinomas with pancreatic cell differentiation. At present there is a preoperative underdiagnosis of these tumours that could be minimized by including this entity in the differential diagnosis of gastric cancer and by performing immunohistochemical analysis with neuroendocrine markers and exocrine pancreatic enzymes.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>35068223</pmid><doi>10.1177/10668969211065763</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9118-9392</orcidid><orcidid>https://orcid.org/0000-0003-2555-0212</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1066-8969 |
| ispartof | International journal of surgical pathology, 2022-08, Vol.30 (5), p.528-538 |
| issn | 1066-8969 1940-2465 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2622478665 |
| source | Access via SAGE; MEDLINE |
| subjects | Biopsy Carcinoma, Acinar Cell - diagnosis Carcinoma, Acinar Cell - pathology Female Gastric cancer Humans Immunohistochemistry Middle Aged Neuroendocrine tumors Pancreas Pancreatic Neoplasms Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - pathology Stomach Neoplasms - diagnosis Stomach Neoplasms - pathology |
| title | Primary Pure Pancreatic -Type Acinar Cell Carcinoma of the Stomach: A Rare Entity with a Difficult Diagnosis and Review of the Literature |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T07%3A14%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Primary%20Pure%20Pancreatic%20-Type%20Acinar%20Cell%20Carcinoma%20of%20the%20Stomach:%20A%20Rare%20Entity%20with%20a%20Difficult%20Diagnosis%20and%20Review%20of%20the%20Literature&rft.jtitle=International%20journal%20of%20surgical%20pathology&rft.au=Paseiro-Crespo,%20Gloria&rft.date=2022-08-01&rft.volume=30&rft.issue=5&rft.spage=528&rft.epage=538&rft.pages=528-538&rft.issn=1066-8969&rft.eissn=1940-2465&rft_id=info:doi/10.1177/10668969211065763&rft_dat=%3Cproquest_cross%3E2622478665%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2685394941&rft_id=info:pmid/35068223&rft_sage_id=10.1177_10668969211065763&rfr_iscdi=true |