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Primary epithelial‐myoepithelial carcinoma of the pituitary gland
Primary salivary gland‐like tumors of the sella are rare and often challenging to diagnose. They reportedly derive from serous and mucinous glands that remain trapped in the infundibulum during embryogenesis. We report a 68‐year‐old man who presented with partial left third cranial nerve palsy, visu...
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Published in: | Neuropathology 2020-06, Vol.40 (3), p.261-267 |
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creator | Lavin, Victoria Callipo, Fabio Donofrio, Carmine A. Ellwood‐Thompson, Rhianedd Metcalf, Robert Djoukhadar, Ibrahim Higham, Claire E. Kearney, Tara Colaco, Rovel Gnanalingham, Kanna Roncaroli, Federico |
description | Primary salivary gland‐like tumors of the sella are rare and often challenging to diagnose. They reportedly derive from serous and mucinous glands that remain trapped in the infundibulum during embryogenesis. We report a 68‐year‐old man who presented with partial left third cranial nerve palsy, visual loss in the left eye without visual field defects, headache, weight loss and reduced muscle bulk. Neuroimaging studies demonstrated a solid and cystic, avidly enhancing lesion expanding the pituitary fossa and extending to the left cavernous sinus. The patient underwent craniotomy and the tissue removed showed features of epithelial‐myoepithelial carcinoma similar to the salivary gland, skin and breast counterpart. No primary tumor was found outside the sella. The lesion behaved aggressively despite radio‐chemotherapy and the patient died 22 months from the onset. The tumor showed a novel TP53 in‐frame deletion (Gly154del) while no variants were found in H‐RAS hotspot regions (codons 12, 13 and 61). Our report expands the spectrum of salivary gland‐like tumors primarily occurring in the sella and emphasizes the need for specialist review of rare, non‐neuroendocrine tumors of the pituitary and sella regions. |
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They reportedly derive from serous and mucinous glands that remain trapped in the infundibulum during embryogenesis. We report a 68‐year‐old man who presented with partial left third cranial nerve palsy, visual loss in the left eye without visual field defects, headache, weight loss and reduced muscle bulk. Neuroimaging studies demonstrated a solid and cystic, avidly enhancing lesion expanding the pituitary fossa and extending to the left cavernous sinus. The patient underwent craniotomy and the tissue removed showed features of epithelial‐myoepithelial carcinoma similar to the salivary gland, skin and breast counterpart. No primary tumor was found outside the sella. The lesion behaved aggressively despite radio‐chemotherapy and the patient died 22 months from the onset. The tumor showed a novel TP53 in‐frame deletion (Gly154del) while no variants were found in H‐RAS hotspot regions (codons 12, 13 and 61). Our report expands the spectrum of salivary gland‐like tumors primarily occurring in the sella and emphasizes the need for specialist review of rare, non‐neuroendocrine tumors of the pituitary and sella regions.</description><identifier>ISSN: 0919-6544</identifier><identifier>EISSN: 1440-1789</identifier><identifier>DOI: 10.1111/neup.12628</identifier><identifier>PMID: 31900996</identifier><language>eng</language><publisher>Melbourne: John Wiley & Sons Australia, Ltd</publisher><subject>Aged ; Breast ; Cancer ; Carcinoma - pathology ; Chemotherapy ; Codons ; Cranial nerves ; Embryogenesis ; epithelial‐myoepithelial carcinoma ; Headache ; Humans ; Male ; Myoepithelioma - pathology ; Neuroendocrine tumors ; Neuroimaging ; p53 Protein ; Paralysis ; Pituitary ; pituitary gland ; Pituitary Neoplasms - pathology ; Salivary gland ; salivary gland‐like tumors ; Tumors ; Visual field</subject><ispartof>Neuropathology, 2020-06, Vol.40 (3), p.261-267</ispartof><rights>2020 Japanese Society of Neuropathology</rights><rights>2020 Japanese Society of Neuropathology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3488-8d64cee7f3caf1c46693b1c09a17870f126509caa8604649a97d579bbfdfa5f83</citedby><cites>FETCH-LOGICAL-c3488-8d64cee7f3caf1c46693b1c09a17870f126509caa8604649a97d579bbfdfa5f83</cites><orcidid>0000-0003-3650-5572</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31900996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lavin, Victoria</creatorcontrib><creatorcontrib>Callipo, Fabio</creatorcontrib><creatorcontrib>Donofrio, Carmine A.</creatorcontrib><creatorcontrib>Ellwood‐Thompson, Rhianedd</creatorcontrib><creatorcontrib>Metcalf, Robert</creatorcontrib><creatorcontrib>Djoukhadar, Ibrahim</creatorcontrib><creatorcontrib>Higham, Claire E.</creatorcontrib><creatorcontrib>Kearney, Tara</creatorcontrib><creatorcontrib>Colaco, Rovel</creatorcontrib><creatorcontrib>Gnanalingham, Kanna</creatorcontrib><creatorcontrib>Roncaroli, Federico</creatorcontrib><title>Primary epithelial‐myoepithelial carcinoma of the pituitary gland</title><title>Neuropathology</title><addtitle>Neuropathology</addtitle><description>Primary salivary gland‐like tumors of the sella are rare and often challenging to diagnose. They reportedly derive from serous and mucinous glands that remain trapped in the infundibulum during embryogenesis. We report a 68‐year‐old man who presented with partial left third cranial nerve palsy, visual loss in the left eye without visual field defects, headache, weight loss and reduced muscle bulk. Neuroimaging studies demonstrated a solid and cystic, avidly enhancing lesion expanding the pituitary fossa and extending to the left cavernous sinus. The patient underwent craniotomy and the tissue removed showed features of epithelial‐myoepithelial carcinoma similar to the salivary gland, skin and breast counterpart. No primary tumor was found outside the sella. The lesion behaved aggressively despite radio‐chemotherapy and the patient died 22 months from the onset. The tumor showed a novel TP53 in‐frame deletion (Gly154del) while no variants were found in H‐RAS hotspot regions (codons 12, 13 and 61). Our report expands the spectrum of salivary gland‐like tumors primarily occurring in the sella and emphasizes the need for specialist review of rare, non‐neuroendocrine tumors of the pituitary and sella regions.</description><subject>Aged</subject><subject>Breast</subject><subject>Cancer</subject><subject>Carcinoma - pathology</subject><subject>Chemotherapy</subject><subject>Codons</subject><subject>Cranial nerves</subject><subject>Embryogenesis</subject><subject>epithelial‐myoepithelial carcinoma</subject><subject>Headache</subject><subject>Humans</subject><subject>Male</subject><subject>Myoepithelioma - pathology</subject><subject>Neuroendocrine tumors</subject><subject>Neuroimaging</subject><subject>p53 Protein</subject><subject>Paralysis</subject><subject>Pituitary</subject><subject>pituitary gland</subject><subject>Pituitary Neoplasms - pathology</subject><subject>Salivary gland</subject><subject>salivary gland‐like tumors</subject><subject>Tumors</subject><subject>Visual field</subject><issn>0919-6544</issn><issn>1440-1789</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtOwzAQhi0EoqWw4QAoEjukFE_iOJ4lqspDqqALurYcx4ZUeeE0Qt1xBM7ISXAJjx3ejDzzzT8zPyGnQKfg32Vt-nYKEY_EHhkDYzSEVOA-GVMEDHnC2Igcdd2aUkgxEodkFANSisjHZLZ0RaXcNjBtsXk2ZaHKj7f3atv8_QOtnC7qplJBYwOfDHypLza7rqdS1fkxObCq7MzJd5yQ1fX8cXYbLh5u7mZXi1DHTIhQ5JxpY1Iba2VBM84xzkBTVH7dlFp_QUJRKyU4ZZyhwjRPUswym1uVWBFPyPmg27rmpTfdRq6b3tV-pIwYRAJohNxTFwOlXdN1zljZDidKoHLnl9z5Jb_88vDZt2SfVSb_RX8M8gAMwGtRmu0_UvJ-vloOop8xgHbU</recordid><startdate>202006</startdate><enddate>202006</enddate><creator>Lavin, Victoria</creator><creator>Callipo, Fabio</creator><creator>Donofrio, Carmine A.</creator><creator>Ellwood‐Thompson, Rhianedd</creator><creator>Metcalf, Robert</creator><creator>Djoukhadar, Ibrahim</creator><creator>Higham, Claire E.</creator><creator>Kearney, Tara</creator><creator>Colaco, Rovel</creator><creator>Gnanalingham, Kanna</creator><creator>Roncaroli, Federico</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, 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>7TK</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0003-3650-5572</orcidid></search><sort><creationdate>202006</creationdate><title>Primary epithelial‐myoepithelial carcinoma of the pituitary gland</title><author>Lavin, Victoria ; Callipo, Fabio ; Donofrio, Carmine A. ; Ellwood‐Thompson, Rhianedd ; Metcalf, Robert ; Djoukhadar, Ibrahim ; Higham, Claire E. ; Kearney, Tara ; Colaco, Rovel ; Gnanalingham, Kanna ; Roncaroli, Federico</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3488-8d64cee7f3caf1c46693b1c09a17870f126509caa8604649a97d579bbfdfa5f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Breast</topic><topic>Cancer</topic><topic>Carcinoma - pathology</topic><topic>Chemotherapy</topic><topic>Codons</topic><topic>Cranial nerves</topic><topic>Embryogenesis</topic><topic>epithelial‐myoepithelial carcinoma</topic><topic>Headache</topic><topic>Humans</topic><topic>Male</topic><topic>Myoepithelioma - pathology</topic><topic>Neuroendocrine tumors</topic><topic>Neuroimaging</topic><topic>p53 Protein</topic><topic>Paralysis</topic><topic>Pituitary</topic><topic>pituitary gland</topic><topic>Pituitary Neoplasms - pathology</topic><topic>Salivary gland</topic><topic>salivary gland‐like tumors</topic><topic>Tumors</topic><topic>Visual field</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lavin, Victoria</creatorcontrib><creatorcontrib>Callipo, Fabio</creatorcontrib><creatorcontrib>Donofrio, Carmine A.</creatorcontrib><creatorcontrib>Ellwood‐Thompson, Rhianedd</creatorcontrib><creatorcontrib>Metcalf, Robert</creatorcontrib><creatorcontrib>Djoukhadar, Ibrahim</creatorcontrib><creatorcontrib>Higham, Claire E.</creatorcontrib><creatorcontrib>Kearney, Tara</creatorcontrib><creatorcontrib>Colaco, Rovel</creatorcontrib><creatorcontrib>Gnanalingham, Kanna</creatorcontrib><creatorcontrib>Roncaroli, Federico</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Neuropathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lavin, Victoria</au><au>Callipo, Fabio</au><au>Donofrio, Carmine A.</au><au>Ellwood‐Thompson, Rhianedd</au><au>Metcalf, Robert</au><au>Djoukhadar, Ibrahim</au><au>Higham, Claire E.</au><au>Kearney, Tara</au><au>Colaco, Rovel</au><au>Gnanalingham, Kanna</au><au>Roncaroli, Federico</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary epithelial‐myoepithelial carcinoma of the pituitary gland</atitle><jtitle>Neuropathology</jtitle><addtitle>Neuropathology</addtitle><date>2020-06</date><risdate>2020</risdate><volume>40</volume><issue>3</issue><spage>261</spage><epage>267</epage><pages>261-267</pages><issn>0919-6544</issn><eissn>1440-1789</eissn><abstract>Primary salivary gland‐like tumors of the sella are rare and often challenging to diagnose. They reportedly derive from serous and mucinous glands that remain trapped in the infundibulum during embryogenesis. We report a 68‐year‐old man who presented with partial left third cranial nerve palsy, visual loss in the left eye without visual field defects, headache, weight loss and reduced muscle bulk. Neuroimaging studies demonstrated a solid and cystic, avidly enhancing lesion expanding the pituitary fossa and extending to the left cavernous sinus. The patient underwent craniotomy and the tissue removed showed features of epithelial‐myoepithelial carcinoma similar to the salivary gland, skin and breast counterpart. No primary tumor was found outside the sella. The lesion behaved aggressively despite radio‐chemotherapy and the patient died 22 months from the onset. The tumor showed a novel TP53 in‐frame deletion (Gly154del) while no variants were found in H‐RAS hotspot regions (codons 12, 13 and 61). Our report expands the spectrum of salivary gland‐like tumors primarily occurring in the sella and emphasizes the need for specialist review of rare, non‐neuroendocrine tumors of the pituitary and sella regions.</abstract><cop>Melbourne</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>31900996</pmid><doi>10.1111/neup.12628</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-3650-5572</orcidid></addata></record> |
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subjects | Aged Breast Cancer Carcinoma - pathology Chemotherapy Codons Cranial nerves Embryogenesis epithelial‐myoepithelial carcinoma Headache Humans Male Myoepithelioma - pathology Neuroendocrine tumors Neuroimaging p53 Protein Paralysis Pituitary pituitary gland Pituitary Neoplasms - pathology Salivary gland salivary gland‐like tumors Tumors Visual field |
title | Primary epithelial‐myoepithelial carcinoma of the pituitary gland |
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