Spontaneous Ganglioneuroma Possibly Originating from the Trigeminal Ganglion in a B6C3F1 Mouse
In a carcinogenicity study, a neuronal tumor in the cranial cavity was observed in a 110-week-old female B6C3F1 mouse. At necropsy, the tumor was seen at the site of the pituitary gland. Histologically, the tumor consisted of well-differentiated ganglion cells, nerve fiber/neuropil-like elements and...
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Veröffentlicht in: | Toxicologic pathology 2009-04, Vol.37 (3), p.343-347 |
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creator | Yasui, Yuzo Ohta, Yasufumi Ueda, Yoshihide Hasegawa, Kazushige Kihara, Tohru Hosoi, Masayo Miyajima, Rumiko Shiga, Atsushi Imai, Kiyoshi Toyoda, Kazuhiro |
description | In a carcinogenicity study, a neuronal tumor in the cranial cavity was observed in a 110-week-old female B6C3F1 mouse. At necropsy, the tumor was seen at the site of the pituitary gland. Histologically, the tumor consisted of well-differentiated ganglion cells, nerve fiber/neuropil-like elements and ganglion-like cells. The tumor was composed mainly of ganglion-like cells, which were arranged in solid sheets interspersed with thin fibrovascular stroma. Nissl substance was detected at the margin in the cytoplasm of well-differentiated ganglion cells, and nerve fibers were identified by the Kluever-Barrera method. Immunohistochemically, the well-differentiated ganglion cells were positive for S-100, neurofilament protein (NF), neuron-specific enolase (NSE), synaptophysin, and chromogranin A. The nerve fiber/neuropil-like elements were positive for S-100, NF, NSE, and glial fibrillary acidic protein (GFAP), and the ganglion-like cells were strongly positive only for NSE and synaptophysin. On the other hand, there were no pituitary cells, such as prolactin-positive or adrenocorticotropic hormone (ACTH)-positive cells in the tumor tissue. Detailed histopathological examination suggested that the tumor might be a ganglioneuroma arising from the trigeminal ganglion. This report provides additional histopathological evidence of peripheral nerve neoplasms in mice. |
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At necropsy, the tumor was seen at the site of the pituitary gland. Histologically, the tumor consisted of well-differentiated ganglion cells, nerve fiber/neuropil-like elements and ganglion-like cells. The tumor was composed mainly of ganglion-like cells, which were arranged in solid sheets interspersed with thin fibrovascular stroma. Nissl substance was detected at the margin in the cytoplasm of well-differentiated ganglion cells, and nerve fibers were identified by the Kluever-Barrera method. Immunohistochemically, the well-differentiated ganglion cells were positive for S-100, neurofilament protein (NF), neuron-specific enolase (NSE), synaptophysin, and chromogranin A. The nerve fiber/neuropil-like elements were positive for S-100, NF, NSE, and glial fibrillary acidic protein (GFAP), and the ganglion-like cells were strongly positive only for NSE and synaptophysin. On the other hand, there were no pituitary cells, such as prolactin-positive or adrenocorticotropic hormone (ACTH)-positive cells in the tumor tissue. Detailed histopathological examination suggested that the tumor might be a ganglioneuroma arising from the trigeminal ganglion. This report provides additional histopathological evidence of peripheral nerve neoplasms in mice.</description><identifier>ISSN: 0192-6233</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1177/0192623309333786</identifier><identifier>PMID: 19380843</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Biological and medical sciences ; Chromogranin A - metabolism ; Female ; Ganglioneuroma - chemistry ; Ganglioneuroma - pathology ; Ganglioneuroma - veterinary ; Glial Fibrillary Acidic Protein - metabolism ; Immunohistochemistry ; Medical sciences ; Mice ; Mice, Inbred Strains ; Neurofilament Proteins - metabolism ; Neurology ; Nissl Bodies - chemistry ; Peripheral Nervous System Neoplasms - chemistry ; Peripheral Nervous System Neoplasms - pathology ; Peripheral Nervous System Neoplasms - veterinary ; Phosphopyruvate Hydratase - metabolism ; Rodent Diseases - metabolism ; Rodent Diseases - pathology ; S100 Proteins - metabolism ; Synaptophysin - metabolism ; Toxicology ; Trigeminal Ganglion - pathology ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Toxicologic pathology, 2009-04, Vol.37 (3), p.343-347</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-3dcb13f2b96d1331b71b100c2297c91b2e420c861c07bba0d4b88178a89fc61a3</citedby><cites>FETCH-LOGICAL-c505t-3dcb13f2b96d1331b71b100c2297c91b2e420c861c07bba0d4b88178a89fc61a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0192623309333786$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0192623309333786$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,781,785,21824,27929,27930,43626,43627</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21300871$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19380843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yasui, Yuzo</creatorcontrib><creatorcontrib>Ohta, Yasufumi</creatorcontrib><creatorcontrib>Ueda, Yoshihide</creatorcontrib><creatorcontrib>Hasegawa, Kazushige</creatorcontrib><creatorcontrib>Kihara, Tohru</creatorcontrib><creatorcontrib>Hosoi, Masayo</creatorcontrib><creatorcontrib>Miyajima, Rumiko</creatorcontrib><creatorcontrib>Shiga, Atsushi</creatorcontrib><creatorcontrib>Imai, Kiyoshi</creatorcontrib><creatorcontrib>Toyoda, Kazuhiro</creatorcontrib><title>Spontaneous Ganglioneuroma Possibly Originating from the Trigeminal Ganglion in a B6C3F1 Mouse</title><title>Toxicologic pathology</title><addtitle>Toxicol Pathol</addtitle><description>In a carcinogenicity study, a neuronal tumor in the cranial cavity was observed in a 110-week-old female B6C3F1 mouse. At necropsy, the tumor was seen at the site of the pituitary gland. Histologically, the tumor consisted of well-differentiated ganglion cells, nerve fiber/neuropil-like elements and ganglion-like cells. The tumor was composed mainly of ganglion-like cells, which were arranged in solid sheets interspersed with thin fibrovascular stroma. Nissl substance was detected at the margin in the cytoplasm of well-differentiated ganglion cells, and nerve fibers were identified by the Kluever-Barrera method. Immunohistochemically, the well-differentiated ganglion cells were positive for S-100, neurofilament protein (NF), neuron-specific enolase (NSE), synaptophysin, and chromogranin A. The nerve fiber/neuropil-like elements were positive for S-100, NF, NSE, and glial fibrillary acidic protein (GFAP), and the ganglion-like cells were strongly positive only for NSE and synaptophysin. On the other hand, there were no pituitary cells, such as prolactin-positive or adrenocorticotropic hormone (ACTH)-positive cells in the tumor tissue. Detailed histopathological examination suggested that the tumor might be a ganglioneuroma arising from the trigeminal ganglion. This report provides additional histopathological evidence of peripheral nerve neoplasms in mice.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chromogranin A - metabolism</subject><subject>Female</subject><subject>Ganglioneuroma - chemistry</subject><subject>Ganglioneuroma - pathology</subject><subject>Ganglioneuroma - veterinary</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Neurofilament Proteins - metabolism</subject><subject>Neurology</subject><subject>Nissl Bodies - chemistry</subject><subject>Peripheral Nervous System Neoplasms - chemistry</subject><subject>Peripheral Nervous System Neoplasms - pathology</subject><subject>Peripheral Nervous System Neoplasms - veterinary</subject><subject>Phosphopyruvate Hydratase - metabolism</subject><subject>Rodent Diseases - metabolism</subject><subject>Rodent Diseases - pathology</subject><subject>S100 Proteins - metabolism</subject><subject>Synaptophysin - metabolism</subject><subject>Toxicology</subject><subject>Trigeminal Ganglion - pathology</subject><subject>Tumors of the nervous system. Phacomatoses</subject><issn>0192-6233</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1LAzEQxYMotlbvniQX8bQ6k2w32aMWq4JSQb26JGm2puxHTXYP_vembFEQPA3M-703zCPkFOESUYgrwJxljHPIOedCZntkjFPOE8wA98l4KydbfUSOQlgDoMQUDskIcy5BpnxM3l82bdOpxrZ9oHeqWVWubWzv21rR5zYEp6svuvBu5RrVuWZFyyjR7sPS17i0dVxXPz7qGqroTTbjc6RPMdEek4NSVcGe7OaEvM1vX2f3yePi7mF2_ZiYKUy7hC-NRl4ynWdL5By1QI0AhrFcmBw1sykDIzM0ILRWsEy1lCikknlpMlR8Qi6G3I1vP3sbuqJ2wdiqGj4rRJphLqdMRhIG0vj4nrdlsfGuVv6rQCi2pRZ_S42Ws114r2u7_DXsWozA-Q5Qwaiq9KoxLvxwDDmAFBi5ZOCCWtli3fY-thf-P_wNr6-KjA</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Yasui, Yuzo</creator><creator>Ohta, Yasufumi</creator><creator>Ueda, Yoshihide</creator><creator>Hasegawa, Kazushige</creator><creator>Kihara, Tohru</creator><creator>Hosoi, Masayo</creator><creator>Miyajima, Rumiko</creator><creator>Shiga, Atsushi</creator><creator>Imai, Kiyoshi</creator><creator>Toyoda, Kazuhiro</creator><general>SAGE Publications</general><general>Sage Publications</general><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20090401</creationdate><title>Spontaneous Ganglioneuroma Possibly Originating from the Trigeminal Ganglion in a B6C3F1 Mouse</title><author>Yasui, Yuzo ; Ohta, Yasufumi ; Ueda, Yoshihide ; Hasegawa, Kazushige ; Kihara, Tohru ; Hosoi, Masayo ; Miyajima, Rumiko ; Shiga, Atsushi ; Imai, Kiyoshi ; Toyoda, Kazuhiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-3dcb13f2b96d1331b71b100c2297c91b2e420c861c07bba0d4b88178a89fc61a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chromogranin A - metabolism</topic><topic>Female</topic><topic>Ganglioneuroma - chemistry</topic><topic>Ganglioneuroma - pathology</topic><topic>Ganglioneuroma - veterinary</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Neurofilament Proteins - metabolism</topic><topic>Neurology</topic><topic>Nissl Bodies - chemistry</topic><topic>Peripheral Nervous System Neoplasms - chemistry</topic><topic>Peripheral Nervous System Neoplasms - pathology</topic><topic>Peripheral Nervous System Neoplasms - veterinary</topic><topic>Phosphopyruvate Hydratase - metabolism</topic><topic>Rodent Diseases - metabolism</topic><topic>Rodent Diseases - pathology</topic><topic>S100 Proteins - metabolism</topic><topic>Synaptophysin - metabolism</topic><topic>Toxicology</topic><topic>Trigeminal Ganglion - pathology</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yasui, Yuzo</creatorcontrib><creatorcontrib>Ohta, Yasufumi</creatorcontrib><creatorcontrib>Ueda, Yoshihide</creatorcontrib><creatorcontrib>Hasegawa, Kazushige</creatorcontrib><creatorcontrib>Kihara, Tohru</creatorcontrib><creatorcontrib>Hosoi, Masayo</creatorcontrib><creatorcontrib>Miyajima, Rumiko</creatorcontrib><creatorcontrib>Shiga, Atsushi</creatorcontrib><creatorcontrib>Imai, Kiyoshi</creatorcontrib><creatorcontrib>Toyoda, Kazuhiro</creatorcontrib><collection>Pascal-Francis</collection><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yasui, Yuzo</au><au>Ohta, Yasufumi</au><au>Ueda, Yoshihide</au><au>Hasegawa, Kazushige</au><au>Kihara, Tohru</au><au>Hosoi, Masayo</au><au>Miyajima, Rumiko</au><au>Shiga, Atsushi</au><au>Imai, Kiyoshi</au><au>Toyoda, Kazuhiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous Ganglioneuroma Possibly Originating from the Trigeminal Ganglion in a B6C3F1 Mouse</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>37</volume><issue>3</issue><spage>343</spage><epage>347</epage><pages>343-347</pages><issn>0192-6233</issn><eissn>1533-1601</eissn><abstract>In a carcinogenicity study, a neuronal tumor in the cranial cavity was observed in a 110-week-old female B6C3F1 mouse. At necropsy, the tumor was seen at the site of the pituitary gland. Histologically, the tumor consisted of well-differentiated ganglion cells, nerve fiber/neuropil-like elements and ganglion-like cells. The tumor was composed mainly of ganglion-like cells, which were arranged in solid sheets interspersed with thin fibrovascular stroma. Nissl substance was detected at the margin in the cytoplasm of well-differentiated ganglion cells, and nerve fibers were identified by the Kluever-Barrera method. Immunohistochemically, the well-differentiated ganglion cells were positive for S-100, neurofilament protein (NF), neuron-specific enolase (NSE), synaptophysin, and chromogranin A. The nerve fiber/neuropil-like elements were positive for S-100, NF, NSE, and glial fibrillary acidic protein (GFAP), and the ganglion-like cells were strongly positive only for NSE and synaptophysin. On the other hand, there were no pituitary cells, such as prolactin-positive or adrenocorticotropic hormone (ACTH)-positive cells in the tumor tissue. Detailed histopathological examination suggested that the tumor might be a ganglioneuroma arising from the trigeminal ganglion. This report provides additional histopathological evidence of peripheral nerve neoplasms in mice.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>19380843</pmid><doi>10.1177/0192623309333786</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Chromogranin A - metabolism Female Ganglioneuroma - chemistry Ganglioneuroma - pathology Ganglioneuroma - veterinary Glial Fibrillary Acidic Protein - metabolism Immunohistochemistry Medical sciences Mice Mice, Inbred Strains Neurofilament Proteins - metabolism Neurology Nissl Bodies - chemistry Peripheral Nervous System Neoplasms - chemistry Peripheral Nervous System Neoplasms - pathology Peripheral Nervous System Neoplasms - veterinary Phosphopyruvate Hydratase - metabolism Rodent Diseases - metabolism Rodent Diseases - pathology S100 Proteins - metabolism Synaptophysin - metabolism Toxicology Trigeminal Ganglion - pathology Tumors of the nervous system. Phacomatoses |
title | Spontaneous Ganglioneuroma Possibly Originating from the Trigeminal Ganglion in a B6C3F1 Mouse |
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