Case Report of Rarely Described Polymorphous Low-Grade Neuroepithelial Tumor of the Young and Comparison with Oligodendroglioma
Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a central nervous system tumor that shares many qualities with oligodendroglioma but is rarely and only very recently described as a distinct entity in the literature. A previously healthy, 19-year-old man presented with new onset...
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| Veröffentlicht in: | World neurosurgery 2019-07, Vol.127, p.47-51 |
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| creator | Sumdani, Hasan Shahbuddin, Zanab Harper, Glenn Hamilton, Lesley |
| description | Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a central nervous system tumor that shares many qualities with oligodendroglioma but is rarely and only very recently described as a distinct entity in the literature.
A previously healthy, 19-year-old man presented with new onset of seizures. Imaging showed an intracranial mass, which was treated with surgical removal. Preoperative and postoperative magnetic resonance imaging, histopathologic examination, genetic testing, and immunohistochemical staining all supported a diagnosis of PLNTY.
Diagnostic investigation of PLNTY shows many similarities with oligodendroglioma, and thus these entities can be mistaken for one another. Certain studies are needed to distinguish PLNTY and other dysembryoplastic neuroepithelial tumors, such as oligodendroglioma. |
| doi_str_mv | 10.1016/j.wneu.2019.03.181 |
| format | Article |
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A previously healthy, 19-year-old man presented with new onset of seizures. Imaging showed an intracranial mass, which was treated with surgical removal. Preoperative and postoperative magnetic resonance imaging, histopathologic examination, genetic testing, and immunohistochemical staining all supported a diagnosis of PLNTY.
Diagnostic investigation of PLNTY shows many similarities with oligodendroglioma, and thus these entities can be mistaken for one another. Certain studies are needed to distinguish PLNTY and other dysembryoplastic neuroepithelial tumors, such as oligodendroglioma.</description><identifier>ISSN: 1878-8750</identifier><identifier>EISSN: 1878-8769</identifier><identifier>DOI: 10.1016/j.wneu.2019.03.181</identifier><identifier>PMID: 30926558</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Brain - diagnostic imaging ; Brain - pathology ; Brain Neoplasms - complications ; Brain Neoplasms - diagnosis ; Brain Neoplasms - genetics ; Brain Neoplasms - pathology ; Diagnosis, Differential ; Dysembryoplastic ; Humans ; Male ; Neoplasm ; Neoplasms, Neuroepithelial - complications ; Neoplasms, Neuroepithelial - diagnosis ; Neoplasms, Neuroepithelial - genetics ; Neoplasms, Neuroepithelial - pathology ; Neurosurgery ; Oligodendroglioma ; Oligodendroglioma - complications ; Oligodendroglioma - diagnosis ; Oligodendroglioma - genetics ; Oligodendroglioma - pathology ; PLNTY ; Polymorphous low-grade neuroepithelial tumor of the young ; Seizure ; Young Adult</subject><ispartof>World neurosurgery, 2019-07, Vol.127, p.47-51</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-b3d5e9309f9e2f627b8eddba3c6f41cde19270fbc330165d0b5c19bcf758a8a93</citedby><cites>FETCH-LOGICAL-c356t-b3d5e9309f9e2f627b8eddba3c6f41cde19270fbc330165d0b5c19bcf758a8a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.wneu.2019.03.181$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30926558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sumdani, Hasan</creatorcontrib><creatorcontrib>Shahbuddin, Zanab</creatorcontrib><creatorcontrib>Harper, Glenn</creatorcontrib><creatorcontrib>Hamilton, Lesley</creatorcontrib><title>Case Report of Rarely Described Polymorphous Low-Grade Neuroepithelial Tumor of the Young and Comparison with Oligodendroglioma</title><title>World neurosurgery</title><addtitle>World Neurosurg</addtitle><description>Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a central nervous system tumor that shares many qualities with oligodendroglioma but is rarely and only very recently described as a distinct entity in the literature.
A previously healthy, 19-year-old man presented with new onset of seizures. Imaging showed an intracranial mass, which was treated with surgical removal. Preoperative and postoperative magnetic resonance imaging, histopathologic examination, genetic testing, and immunohistochemical staining all supported a diagnosis of PLNTY.
Diagnostic investigation of PLNTY shows many similarities with oligodendroglioma, and thus these entities can be mistaken for one another. Certain studies are needed to distinguish PLNTY and other dysembryoplastic neuroepithelial tumors, such as oligodendroglioma.</description><subject>Adult</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - pathology</subject><subject>Brain Neoplasms - complications</subject><subject>Brain Neoplasms - diagnosis</subject><subject>Brain Neoplasms - genetics</subject><subject>Brain Neoplasms - pathology</subject><subject>Diagnosis, Differential</subject><subject>Dysembryoplastic</subject><subject>Humans</subject><subject>Male</subject><subject>Neoplasm</subject><subject>Neoplasms, Neuroepithelial - complications</subject><subject>Neoplasms, Neuroepithelial - diagnosis</subject><subject>Neoplasms, Neuroepithelial - genetics</subject><subject>Neoplasms, Neuroepithelial - pathology</subject><subject>Neurosurgery</subject><subject>Oligodendroglioma</subject><subject>Oligodendroglioma - complications</subject><subject>Oligodendroglioma - diagnosis</subject><subject>Oligodendroglioma - genetics</subject><subject>Oligodendroglioma - pathology</subject><subject>PLNTY</subject><subject>Polymorphous low-grade neuroepithelial tumor of the young</subject><subject>Seizure</subject><subject>Young Adult</subject><issn>1878-8750</issn><issn>1878-8769</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQhq2KqiDgD_RQ-dhLgj9w4khc0NIC0goqBAdOlmNPFq-cOLWTrvbUv45XCxzxZazRM69mHoS-U1JSQquzdbkZYC4ZoU1JeEkl_YKOqKxlIeuqOfj4C3KITlNak_w4PZc1_4YOOWlYJYQ8Qv8XOgF-gDHECYcOP-gIfouvIJnoWrD4T_DbPsTxJcwJL8OmuI7aAr6DOQYY3fQC3mmPH-cM7QJyAz-HeVhhPVi8CP2oo0thwJvM4nvvVsHCYGNYeRd6fYK-dtonOH2rx-jp96_HxU2xvL--XVwuC8NFNRUttwKavHbXAOsqVrcSrG01N1V3To0F2rCadK3hPMsRlrTC0KY1XS2klrrhx-jnPneM4e8MaVK9Swa81wPkyxRjhNSSMMEyyvaoiSGlCJ0ao-t13CpK1M69Wqude7VzrwhX2X0e-vGWP7c92I-Rd9MZuNgDkK_85yCqZBwMBqyLYCZlg_ss_xUCnpgW</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Sumdani, Hasan</creator><creator>Shahbuddin, Zanab</creator><creator>Harper, Glenn</creator><creator>Hamilton, Lesley</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>201907</creationdate><title>Case Report of Rarely Described Polymorphous Low-Grade Neuroepithelial Tumor of the Young and Comparison with Oligodendroglioma</title><author>Sumdani, Hasan ; Shahbuddin, Zanab ; Harper, Glenn ; Hamilton, Lesley</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-b3d5e9309f9e2f627b8eddba3c6f41cde19270fbc330165d0b5c19bcf758a8a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - pathology</topic><topic>Brain Neoplasms - complications</topic><topic>Brain Neoplasms - diagnosis</topic><topic>Brain Neoplasms - genetics</topic><topic>Brain Neoplasms - pathology</topic><topic>Diagnosis, Differential</topic><topic>Dysembryoplastic</topic><topic>Humans</topic><topic>Male</topic><topic>Neoplasm</topic><topic>Neoplasms, Neuroepithelial - complications</topic><topic>Neoplasms, Neuroepithelial - diagnosis</topic><topic>Neoplasms, Neuroepithelial - genetics</topic><topic>Neoplasms, Neuroepithelial - pathology</topic><topic>Neurosurgery</topic><topic>Oligodendroglioma</topic><topic>Oligodendroglioma - complications</topic><topic>Oligodendroglioma - diagnosis</topic><topic>Oligodendroglioma - genetics</topic><topic>Oligodendroglioma - pathology</topic><topic>PLNTY</topic><topic>Polymorphous low-grade neuroepithelial tumor of the young</topic><topic>Seizure</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sumdani, Hasan</creatorcontrib><creatorcontrib>Shahbuddin, Zanab</creatorcontrib><creatorcontrib>Harper, Glenn</creatorcontrib><creatorcontrib>Hamilton, Lesley</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>World neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sumdani, Hasan</au><au>Shahbuddin, Zanab</au><au>Harper, Glenn</au><au>Hamilton, Lesley</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Case Report of Rarely Described Polymorphous Low-Grade Neuroepithelial Tumor of the Young and Comparison with Oligodendroglioma</atitle><jtitle>World neurosurgery</jtitle><addtitle>World Neurosurg</addtitle><date>2019-07</date><risdate>2019</risdate><volume>127</volume><spage>47</spage><epage>51</epage><pages>47-51</pages><issn>1878-8750</issn><eissn>1878-8769</eissn><abstract>Polymorphous low-grade neuroepithelial tumor of the young (PLNTY) is a central nervous system tumor that shares many qualities with oligodendroglioma but is rarely and only very recently described as a distinct entity in the literature.
A previously healthy, 19-year-old man presented with new onset of seizures. Imaging showed an intracranial mass, which was treated with surgical removal. Preoperative and postoperative magnetic resonance imaging, histopathologic examination, genetic testing, and immunohistochemical staining all supported a diagnosis of PLNTY.
Diagnostic investigation of PLNTY shows many similarities with oligodendroglioma, and thus these entities can be mistaken for one another. Certain studies are needed to distinguish PLNTY and other dysembryoplastic neuroepithelial tumors, such as oligodendroglioma.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30926558</pmid><doi>10.1016/j.wneu.2019.03.181</doi><tpages>5</tpages></addata></record> |
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| subjects | Adult Brain - diagnostic imaging Brain - pathology Brain Neoplasms - complications Brain Neoplasms - diagnosis Brain Neoplasms - genetics Brain Neoplasms - pathology Diagnosis, Differential Dysembryoplastic Humans Male Neoplasm Neoplasms, Neuroepithelial - complications Neoplasms, Neuroepithelial - diagnosis Neoplasms, Neuroepithelial - genetics Neoplasms, Neuroepithelial - pathology Neurosurgery Oligodendroglioma Oligodendroglioma - complications Oligodendroglioma - diagnosis Oligodendroglioma - genetics Oligodendroglioma - pathology PLNTY Polymorphous low-grade neuroepithelial tumor of the young Seizure Young Adult |
| title | Case Report of Rarely Described Polymorphous Low-Grade Neuroepithelial Tumor of the Young and Comparison with Oligodendroglioma |
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