Localized overexpression of alpha‐internexin within nodules in multinodular and vacuolating neuronal tumors
Multinodular and vacuolating neuronal tumors (MVNT) have been recently referred to as a distinctive neuronal tumor entity based on histopathological findings. They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only...
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Veröffentlicht in: | Neuropathology 2015-12, Vol.35 (6), p.561-568 |
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description | Multinodular and vacuolating neuronal tumors (MVNT) have been recently referred to as a distinctive neuronal tumor entity based on histopathological findings. They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only 13 cases have been reported in the literature to date and little is known about the histopathology of these tumors. Herein, we report a case of MVNT with additional confirmation of immunohistochemical features. A 22‐year‐old woman presented with a continuous headache. MRI showed a subcortical white matter lesion with multiple satellite nodules in the frontal lobe appearing as T2/fluid‐attenuated inversion recovery (FLAIR) hyperintensities. Histological examination of the resected lesion revealed well‐defined multiple nodules composed of predominant vacuolating tumor cells. The tumor cells exhibited consistent immunolabeling for doublecortin, as well as HuC/HuD, both representative neuronal biomarkers associated with earlier stages of neuronal development. Immunopositivity for oligodendrocyte transcription factor 2 (Olig2) and S100 was also detected in tumor cells. Additionally, significant overexpression of alpha‐internexin was observed in the background neuropil limited to tumor nodules. Neuronal nuclear antigen (NeuN), synaptophysin and neurofilament, markers for mature neurons, were either negative or weakly positive. The expression profile of neuronal biomarkers can be distinguished from that of classic neuronal tumors and is the immunohistochemical hallmark of MVNT. In summary, we identified the characteristic tumoral expression of HuC/HuD and doublecortin and the presence of abundant neuropil localized in MVNT tumor nodules, which exhibited widespread alpha‐internexin expression. These results supported the presumption that MVNT is a distinct histopathological entity. |
doi_str_mv | 10.1111/neup.12217 |
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They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only 13 cases have been reported in the literature to date and little is known about the histopathology of these tumors. Herein, we report a case of MVNT with additional confirmation of immunohistochemical features. A 22‐year‐old woman presented with a continuous headache. MRI showed a subcortical white matter lesion with multiple satellite nodules in the frontal lobe appearing as T2/fluid‐attenuated inversion recovery (FLAIR) hyperintensities. Histological examination of the resected lesion revealed well‐defined multiple nodules composed of predominant vacuolating tumor cells. The tumor cells exhibited consistent immunolabeling for doublecortin, as well as HuC/HuD, both representative neuronal biomarkers associated with earlier stages of neuronal development. Immunopositivity for oligodendrocyte transcription factor 2 (Olig2) and S100 was also detected in tumor cells. Additionally, significant overexpression of alpha‐internexin was observed in the background neuropil limited to tumor nodules. Neuronal nuclear antigen (NeuN), synaptophysin and neurofilament, markers for mature neurons, were either negative or weakly positive. The expression profile of neuronal biomarkers can be distinguished from that of classic neuronal tumors and is the immunohistochemical hallmark of MVNT. In summary, we identified the characteristic tumoral expression of HuC/HuD and doublecortin and the presence of abundant neuropil localized in MVNT tumor nodules, which exhibited widespread alpha‐internexin expression. These results supported the presumption that MVNT is a distinct histopathological entity.</description><identifier>ISSN: 0919-6544</identifier><identifier>EISSN: 1440-1789</identifier><identifier>DOI: 10.1111/neup.12217</identifier><identifier>PMID: 26073706</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Biomarkers ; Biomarkers, Tumor - analysis ; Brain Neoplasms - pathology ; ELAV-Like Protein 3 - analysis ; ELAV-Like Protein 3 - biosynthesis ; ELAV-Like Protein 4 - analysis ; ELAV-Like Protein 4 - biosynthesis ; Female ; ganglioglioma ; HuC/HuD ; Humans ; Intermediate Filament Proteins - analysis ; Intermediate Filament Proteins - biosynthesis ; internexin ; Microtubule-Associated Proteins - analysis ; Microtubule-Associated Proteins - biosynthesis ; multinodular ; neuronal tumor ; Neurons - pathology ; Neuropeptides - analysis ; Neuropeptides - biosynthesis ; Tumors ; Up-Regulation ; Vacuoles - pathology ; Young Adult</subject><ispartof>Neuropathology, 2015-12, Vol.35 (6), p.561-568</ispartof><rights>2015 Japanese Society of Neuropathology</rights><rights>2015 Japanese Society of Neuropathology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5507-904445089ab171698d7693aad62dfc3805262b29cae9fd77a41b0f98630d41383</citedby><cites>FETCH-LOGICAL-c5507-904445089ab171698d7693aad62dfc3805262b29cae9fd77a41b0f98630d41383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fneup.12217$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fneup.12217$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26073706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagaishi, Masaya</creatorcontrib><creatorcontrib>Yokoo, Hideaki</creatorcontrib><creatorcontrib>Nobusawa, Sumihito</creatorcontrib><creatorcontrib>Fujii, Yoshiko</creatorcontrib><creatorcontrib>Sugiura, Yoshiki</creatorcontrib><creatorcontrib>Suzuki, Ryotaro</creatorcontrib><creatorcontrib>Tanaka, Yoshihiro</creatorcontrib><creatorcontrib>Suzuki, Kensuke</creatorcontrib><creatorcontrib>Hyodo, Akio</creatorcontrib><title>Localized overexpression of alpha‐internexin within nodules in multinodular and vacuolating neuronal tumors</title><title>Neuropathology</title><addtitle>Neuropathology</addtitle><description>Multinodular and vacuolating neuronal tumors (MVNT) have been recently referred to as a distinctive neuronal tumor entity based on histopathological findings. They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only 13 cases have been reported in the literature to date and little is known about the histopathology of these tumors. Herein, we report a case of MVNT with additional confirmation of immunohistochemical features. A 22‐year‐old woman presented with a continuous headache. MRI showed a subcortical white matter lesion with multiple satellite nodules in the frontal lobe appearing as T2/fluid‐attenuated inversion recovery (FLAIR) hyperintensities. Histological examination of the resected lesion revealed well‐defined multiple nodules composed of predominant vacuolating tumor cells. The tumor cells exhibited consistent immunolabeling for doublecortin, as well as HuC/HuD, both representative neuronal biomarkers associated with earlier stages of neuronal development. Immunopositivity for oligodendrocyte transcription factor 2 (Olig2) and S100 was also detected in tumor cells. Additionally, significant overexpression of alpha‐internexin was observed in the background neuropil limited to tumor nodules. Neuronal nuclear antigen (NeuN), synaptophysin and neurofilament, markers for mature neurons, were either negative or weakly positive. The expression profile of neuronal biomarkers can be distinguished from that of classic neuronal tumors and is the immunohistochemical hallmark of MVNT. In summary, we identified the characteristic tumoral expression of HuC/HuD and doublecortin and the presence of abundant neuropil localized in MVNT tumor nodules, which exhibited widespread alpha‐internexin expression. These results supported the presumption that MVNT is a distinct histopathological entity.</description><subject>Biomarkers</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Brain Neoplasms - pathology</subject><subject>ELAV-Like Protein 3 - analysis</subject><subject>ELAV-Like Protein 3 - biosynthesis</subject><subject>ELAV-Like Protein 4 - analysis</subject><subject>ELAV-Like Protein 4 - biosynthesis</subject><subject>Female</subject><subject>ganglioglioma</subject><subject>HuC/HuD</subject><subject>Humans</subject><subject>Intermediate Filament Proteins - analysis</subject><subject>Intermediate Filament Proteins - biosynthesis</subject><subject>internexin</subject><subject>Microtubule-Associated Proteins - analysis</subject><subject>Microtubule-Associated Proteins - biosynthesis</subject><subject>multinodular</subject><subject>neuronal tumor</subject><subject>Neurons - pathology</subject><subject>Neuropeptides - analysis</subject><subject>Neuropeptides - biosynthesis</subject><subject>Tumors</subject><subject>Up-Regulation</subject><subject>Vacuoles - pathology</subject><subject>Young Adult</subject><issn>0919-6544</issn><issn>1440-1789</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkbtOHDEUhq0oKGwgTR4gspQmijTEt_GlRIgA0gpSQD3yjj3ByGMP9phLqjwCz5gniZcFCorkNOfY-vQdWz8AHzHaw7W-BVumPUwIFm_AAjOGGiykegsWSGHV8JaxbfA-5yuEsFBEvgPbhCNBBeILMC5jr737ZQ2MNzbZuynZnF0MMA5Q--lS__n94MJsU7B3LsBbN1_WFqIp3mZYx7H42T2edYI6GHij-xK9rpc_YX1aikF7OJcxprwLtgbts_3w1HfAxffD84PjZnl2dHKwv2z6tkWiUYgx1iKp9AoLzJU0giuqteHEDD2VqCWcrIjqtVWDEUIzvEKDkpwiwzCVdAd82XinFK-LzXM3utxb73WwseQOixYTilCF_48yxjmpCyv6-RV6FUuqv1tTVMqWUb4Wft1QfYo5Jzt0U3KjTvcdRt06r26dV_eYV4U_PSnLarTmBX0OqAJ4A9w6b-__oepODy9-bKR_AYPtoa4</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Nagaishi, Masaya</creator><creator>Yokoo, Hideaki</creator><creator>Nobusawa, Sumihito</creator><creator>Fujii, Yoshiko</creator><creator>Sugiura, Yoshiki</creator><creator>Suzuki, Ryotaro</creator><creator>Tanaka, Yoshihiro</creator><creator>Suzuki, Kensuke</creator><creator>Hyodo, Akio</creator><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><scope>7X8</scope></search><sort><creationdate>201512</creationdate><title>Localized overexpression of alpha‐internexin within nodules in multinodular and vacuolating neuronal tumors</title><author>Nagaishi, Masaya ; Yokoo, Hideaki ; Nobusawa, Sumihito ; Fujii, Yoshiko ; Sugiura, Yoshiki ; Suzuki, Ryotaro ; Tanaka, Yoshihiro ; Suzuki, Kensuke ; Hyodo, Akio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5507-904445089ab171698d7693aad62dfc3805262b29cae9fd77a41b0f98630d41383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biomarkers</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Brain Neoplasms - pathology</topic><topic>ELAV-Like Protein 3 - analysis</topic><topic>ELAV-Like Protein 3 - biosynthesis</topic><topic>ELAV-Like Protein 4 - analysis</topic><topic>ELAV-Like Protein 4 - biosynthesis</topic><topic>Female</topic><topic>ganglioglioma</topic><topic>HuC/HuD</topic><topic>Humans</topic><topic>Intermediate Filament Proteins - analysis</topic><topic>Intermediate Filament Proteins - biosynthesis</topic><topic>internexin</topic><topic>Microtubule-Associated Proteins - analysis</topic><topic>Microtubule-Associated Proteins - biosynthesis</topic><topic>multinodular</topic><topic>neuronal tumor</topic><topic>Neurons - pathology</topic><topic>Neuropeptides - analysis</topic><topic>Neuropeptides - biosynthesis</topic><topic>Tumors</topic><topic>Up-Regulation</topic><topic>Vacuoles - pathology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagaishi, Masaya</creatorcontrib><creatorcontrib>Yokoo, Hideaki</creatorcontrib><creatorcontrib>Nobusawa, Sumihito</creatorcontrib><creatorcontrib>Fujii, Yoshiko</creatorcontrib><creatorcontrib>Sugiura, Yoshiki</creatorcontrib><creatorcontrib>Suzuki, Ryotaro</creatorcontrib><creatorcontrib>Tanaka, Yoshihiro</creatorcontrib><creatorcontrib>Suzuki, Kensuke</creatorcontrib><creatorcontrib>Hyodo, Akio</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><collection>MEDLINE - Academic</collection><jtitle>Neuropathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagaishi, Masaya</au><au>Yokoo, Hideaki</au><au>Nobusawa, Sumihito</au><au>Fujii, Yoshiko</au><au>Sugiura, Yoshiki</au><au>Suzuki, Ryotaro</au><au>Tanaka, Yoshihiro</au><au>Suzuki, Kensuke</au><au>Hyodo, Akio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localized overexpression of alpha‐internexin within nodules in multinodular and vacuolating neuronal tumors</atitle><jtitle>Neuropathology</jtitle><addtitle>Neuropathology</addtitle><date>2015-12</date><risdate>2015</risdate><volume>35</volume><issue>6</issue><spage>561</spage><epage>568</epage><pages>561-568</pages><issn>0919-6544</issn><eissn>1440-1789</eissn><abstract>Multinodular and vacuolating neuronal tumors (MVNT) have been recently referred to as a distinctive neuronal tumor entity based on histopathological findings. They are characterized by multiple tumor nodules, vacuolar alteration and widespread immunolabeling for human neuronal protein HuC/HuD. Only 13 cases have been reported in the literature to date and little is known about the histopathology of these tumors. Herein, we report a case of MVNT with additional confirmation of immunohistochemical features. A 22‐year‐old woman presented with a continuous headache. MRI showed a subcortical white matter lesion with multiple satellite nodules in the frontal lobe appearing as T2/fluid‐attenuated inversion recovery (FLAIR) hyperintensities. Histological examination of the resected lesion revealed well‐defined multiple nodules composed of predominant vacuolating tumor cells. The tumor cells exhibited consistent immunolabeling for doublecortin, as well as HuC/HuD, both representative neuronal biomarkers associated with earlier stages of neuronal development. Immunopositivity for oligodendrocyte transcription factor 2 (Olig2) and S100 was also detected in tumor cells. Additionally, significant overexpression of alpha‐internexin was observed in the background neuropil limited to tumor nodules. Neuronal nuclear antigen (NeuN), synaptophysin and neurofilament, markers for mature neurons, were either negative or weakly positive. The expression profile of neuronal biomarkers can be distinguished from that of classic neuronal tumors and is the immunohistochemical hallmark of MVNT. In summary, we identified the characteristic tumoral expression of HuC/HuD and doublecortin and the presence of abundant neuropil localized in MVNT tumor nodules, which exhibited widespread alpha‐internexin expression. These results supported the presumption that MVNT is a distinct histopathological entity.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>26073706</pmid><doi>10.1111/neup.12217</doi><tpages>8</tpages></addata></record> |
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subjects | Biomarkers Biomarkers, Tumor - analysis Brain Neoplasms - pathology ELAV-Like Protein 3 - analysis ELAV-Like Protein 3 - biosynthesis ELAV-Like Protein 4 - analysis ELAV-Like Protein 4 - biosynthesis Female ganglioglioma HuC/HuD Humans Intermediate Filament Proteins - analysis Intermediate Filament Proteins - biosynthesis internexin Microtubule-Associated Proteins - analysis Microtubule-Associated Proteins - biosynthesis multinodular neuronal tumor Neurons - pathology Neuropeptides - analysis Neuropeptides - biosynthesis Tumors Up-Regulation Vacuoles - pathology Young Adult |
title | Localized overexpression of alpha‐internexin within nodules in multinodular and vacuolating neuronal tumors |
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