Aggressive large cell medulloblastoma extending to the extracranial region in brain-dead state
Introduction The authors describe the case of a 29-month-old boy who presented with acute non-communicating hydrocephalus caused by a small tumor in the fourth ventricle. He became brain-dead immediately and remained stable in that condition. Materials and methods Six months later, despite being in...
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creator | Miwa, Tomoru Oi, Shizuo Nonaka, Yuichiro Tamogami, Ryo Sasaki, Hikaru Yoshinari, Satoshi Ida, Hiroyuki |
description | Introduction
The authors describe the case of a 29-month-old boy who presented with acute non-communicating hydrocephalus caused by a small tumor in the fourth ventricle. He became brain-dead immediately and remained stable in that condition.
Materials and methods
Six months later, despite being in a brain-dead state, a rapid direct tumor extension from the intracranial to extracranial region was observed, and chemoradiotherapy was performed following tumor biopsy. The histopathological diagnosis was large cell medulloblastoma. Although treatment was initially effective, the tumor again aggressively invaded the cervical muscles via the spinal canal. Comparative genomic hybridization (metaphase) analysis revealed a pattern of aberrations predictive of a poor prognosis (+1q, ?17p, +17q, and probable amplification of
c-myc
gene), and he eventually died 11 months after onset.
Results
Direct invasion of medulloblastoma from the intracranial to extracranial region is extremely rare, and, to our knowledge, this is the first report of medulloblastoma exhibiting rapid extension to the extracranial region in brain-dead state.
Conclusions
For patients with medulloblastomas, careful observation is needed even in brain-dead state. The etiology of this rare condition as well as the genetic characteristics responsible for aggressive tumor behavior are discussed. |
doi_str_mv | 10.1007/s00381-011-1450-9 |
format | Article |
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The authors describe the case of a 29-month-old boy who presented with acute non-communicating hydrocephalus caused by a small tumor in the fourth ventricle. He became brain-dead immediately and remained stable in that condition.
Materials and methods
Six months later, despite being in a brain-dead state, a rapid direct tumor extension from the intracranial to extracranial region was observed, and chemoradiotherapy was performed following tumor biopsy. The histopathological diagnosis was large cell medulloblastoma. Although treatment was initially effective, the tumor again aggressively invaded the cervical muscles via the spinal canal. Comparative genomic hybridization (metaphase) analysis revealed a pattern of aberrations predictive of a poor prognosis (+1q, ?17p, +17q, and probable amplification of
c-myc
gene), and he eventually died 11 months after onset.
Results
Direct invasion of medulloblastoma from the intracranial to extracranial region is extremely rare, and, to our knowledge, this is the first report of medulloblastoma exhibiting rapid extension to the extracranial region in brain-dead state.
Conclusions
For patients with medulloblastomas, careful observation is needed even in brain-dead state. The etiology of this rare condition as well as the genetic characteristics responsible for aggressive tumor behavior are discussed.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-011-1450-9</identifier><identifier>PMID: 21533576</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Brain Death - pathology ; Case Report ; Cerebellar Neoplasms - genetics ; Cerebellar Neoplasms - pathology ; Cerebellar Neoplasms - physiopathology ; Child, Preschool ; Humans ; Male ; Medicine ; Medicine & Public Health ; Medulloblastoma - genetics ; Medulloblastoma - pathology ; Medulloblastoma - physiopathology ; Neurosciences ; Neurosurgery</subject><ispartof>Child's nervous system, 2011-08, Vol.27 (8), p.1341-1346</ispartof><rights>Springer-Verlag 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p215t-77929046d50c0f55bc52bf1010f768f7b291a8e5cc396d2b6891d084b2fdca683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00381-011-1450-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00381-011-1450-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21533576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miwa, Tomoru</creatorcontrib><creatorcontrib>Oi, Shizuo</creatorcontrib><creatorcontrib>Nonaka, Yuichiro</creatorcontrib><creatorcontrib>Tamogami, Ryo</creatorcontrib><creatorcontrib>Sasaki, Hikaru</creatorcontrib><creatorcontrib>Yoshinari, Satoshi</creatorcontrib><creatorcontrib>Ida, Hiroyuki</creatorcontrib><title>Aggressive large cell medulloblastoma extending to the extracranial region in brain-dead state</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><addtitle>Childs Nerv Syst</addtitle><description>Introduction
The authors describe the case of a 29-month-old boy who presented with acute non-communicating hydrocephalus caused by a small tumor in the fourth ventricle. He became brain-dead immediately and remained stable in that condition.
Materials and methods
Six months later, despite being in a brain-dead state, a rapid direct tumor extension from the intracranial to extracranial region was observed, and chemoradiotherapy was performed following tumor biopsy. The histopathological diagnosis was large cell medulloblastoma. Although treatment was initially effective, the tumor again aggressively invaded the cervical muscles via the spinal canal. Comparative genomic hybridization (metaphase) analysis revealed a pattern of aberrations predictive of a poor prognosis (+1q, ?17p, +17q, and probable amplification of
c-myc
gene), and he eventually died 11 months after onset.
Results
Direct invasion of medulloblastoma from the intracranial to extracranial region is extremely rare, and, to our knowledge, this is the first report of medulloblastoma exhibiting rapid extension to the extracranial region in brain-dead state.
Conclusions
For patients with medulloblastomas, careful observation is needed even in brain-dead state. The etiology of this rare condition as well as the genetic characteristics responsible for aggressive tumor behavior are discussed.</description><subject>Brain Death - pathology</subject><subject>Case Report</subject><subject>Cerebellar Neoplasms - genetics</subject><subject>Cerebellar Neoplasms - pathology</subject><subject>Cerebellar Neoplasms - physiopathology</subject><subject>Child, Preschool</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medulloblastoma - genetics</subject><subject>Medulloblastoma - pathology</subject><subject>Medulloblastoma - physiopathology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1LxDAQhoMo7rr6A7xIbp6ik6RJmuMifsGCF70a0jatXdp0TVrRf2_KrmdPAzMPw8z7IHRJ4YYCqNsIwHNKgFJCMwFEH6ElzTgnwAUcoyUwIYmCDBboLMYtABU506dowajgXCi5RO_rpgkuxvbL4c6GxuHSdR3uXTV13VB0No5Db7H7Hp2vWt_gccDjh5sbwZbB-tZ2OLimHTxuPS6CbT2pnK1wHO3oztFJbbvoLg51hd4e7l_vnsjm5fH5br0hu3TKSJTSTEMmKwEl1EIUpWBFTYFCrWReq4JpanMnypJrWbFC5ppWkGcFq6vSypyv0PV-7y4Mn5OLo-nbOH9ivRumaDQFmUktsn_JXCWWKy4TeXUgpyLlYXah7W34MX_hJYDtgZhGvnHBbIcp-PSnoWBmQ2ZvyCRDZjZkNP8FIvuBKA</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Miwa, Tomoru</creator><creator>Oi, Shizuo</creator><creator>Nonaka, Yuichiro</creator><creator>Tamogami, Ryo</creator><creator>Sasaki, Hikaru</creator><creator>Yoshinari, Satoshi</creator><creator>Ida, Hiroyuki</creator><general>Springer-Verlag</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20110801</creationdate><title>Aggressive large cell medulloblastoma extending to the extracranial region in brain-dead state</title><author>Miwa, Tomoru ; Oi, Shizuo ; Nonaka, Yuichiro ; Tamogami, Ryo ; Sasaki, Hikaru ; Yoshinari, Satoshi ; Ida, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p215t-77929046d50c0f55bc52bf1010f768f7b291a8e5cc396d2b6891d084b2fdca683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Brain Death - pathology</topic><topic>Case Report</topic><topic>Cerebellar Neoplasms - genetics</topic><topic>Cerebellar Neoplasms - pathology</topic><topic>Cerebellar Neoplasms - physiopathology</topic><topic>Child, Preschool</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medulloblastoma - genetics</topic><topic>Medulloblastoma - pathology</topic><topic>Medulloblastoma - physiopathology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miwa, Tomoru</creatorcontrib><creatorcontrib>Oi, Shizuo</creatorcontrib><creatorcontrib>Nonaka, Yuichiro</creatorcontrib><creatorcontrib>Tamogami, Ryo</creatorcontrib><creatorcontrib>Sasaki, Hikaru</creatorcontrib><creatorcontrib>Yoshinari, Satoshi</creatorcontrib><creatorcontrib>Ida, Hiroyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miwa, Tomoru</au><au>Oi, Shizuo</au><au>Nonaka, Yuichiro</au><au>Tamogami, Ryo</au><au>Sasaki, Hikaru</au><au>Yoshinari, Satoshi</au><au>Ida, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aggressive large cell medulloblastoma extending to the extracranial region in brain-dead state</atitle><jtitle>Child's nervous system</jtitle><stitle>Childs Nerv Syst</stitle><addtitle>Childs Nerv Syst</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>27</volume><issue>8</issue><spage>1341</spage><epage>1346</epage><pages>1341-1346</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Introduction
The authors describe the case of a 29-month-old boy who presented with acute non-communicating hydrocephalus caused by a small tumor in the fourth ventricle. He became brain-dead immediately and remained stable in that condition.
Materials and methods
Six months later, despite being in a brain-dead state, a rapid direct tumor extension from the intracranial to extracranial region was observed, and chemoradiotherapy was performed following tumor biopsy. The histopathological diagnosis was large cell medulloblastoma. Although treatment was initially effective, the tumor again aggressively invaded the cervical muscles via the spinal canal. Comparative genomic hybridization (metaphase) analysis revealed a pattern of aberrations predictive of a poor prognosis (+1q, ?17p, +17q, and probable amplification of
c-myc
gene), and he eventually died 11 months after onset.
Results
Direct invasion of medulloblastoma from the intracranial to extracranial region is extremely rare, and, to our knowledge, this is the first report of medulloblastoma exhibiting rapid extension to the extracranial region in brain-dead state.
Conclusions
For patients with medulloblastomas, careful observation is needed even in brain-dead state. The etiology of this rare condition as well as the genetic characteristics responsible for aggressive tumor behavior are discussed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21533576</pmid><doi>10.1007/s00381-011-1450-9</doi><tpages>6</tpages></addata></record> |
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subjects | Brain Death - pathology Case Report Cerebellar Neoplasms - genetics Cerebellar Neoplasms - pathology Cerebellar Neoplasms - physiopathology Child, Preschool Humans Male Medicine Medicine & Public Health Medulloblastoma - genetics Medulloblastoma - pathology Medulloblastoma - physiopathology Neurosciences Neurosurgery |
title | Aggressive large cell medulloblastoma extending to the extracranial region in brain-dead state |
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