A case of postoperative cerebellar mutism with hyperphagia in a child following gross total resection of medulloblastoma occupying the cerebellar vermis
Introduction Cerebellar mutism syndrome is a well-known complication following posterior fossa tumor resection. Its incidence is markedly increased among patients with medulloblastoma. Patients typically present with an inability to communicate verbally due to disruption of the dentato-thalamocortic...
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| Veröffentlicht in: | Child's nervous system 2022-11, Vol.38 (11), p.2189-2198 |
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| creator | Alharbi, Shatha Bawazir, Minyal Altweijri, Ikhlass |
| description | Introduction
Cerebellar mutism syndrome is a well-known complication following posterior fossa tumor resection. Its incidence is markedly increased among patients with medulloblastoma. Patients typically present with an inability to communicate verbally due to disruption of the dentato-thalamocortical pathway.
Case Description
We present a unique case of cerebellar mutism in a three-year-old girl who underwent gross total resection of medulloblastoma occupying the cerebellar vermis. In addition to mutism, the patient developed hyperphagia.
Discussion
This case report aims to contribute to current understanding of the role of cerebello-hypothalamic connections in cerebellar mutism and their clinical significance. |
| doi_str_mv | 10.1007/s00381-022-05520-9 |
| format | Article |
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Cerebellar mutism syndrome is a well-known complication following posterior fossa tumor resection. Its incidence is markedly increased among patients with medulloblastoma. Patients typically present with an inability to communicate verbally due to disruption of the dentato-thalamocortical pathway.
Case Description
We present a unique case of cerebellar mutism in a three-year-old girl who underwent gross total resection of medulloblastoma occupying the cerebellar vermis. In addition to mutism, the patient developed hyperphagia.
Discussion
This case report aims to contribute to current understanding of the role of cerebello-hypothalamic connections in cerebellar mutism and their clinical significance.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-022-05520-9</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Case Report ; Medicine ; Medicine & Public Health ; Neurosciences ; Neurosurgery</subject><ispartof>Child's nervous system, 2022-11, Vol.38 (11), p.2189-2198</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c254t-740baebc146132cea6dc67e8d62fe128bdc79fe4dd591b1c0b861c3e01b6097f3</citedby><cites>FETCH-LOGICAL-c254t-740baebc146132cea6dc67e8d62fe128bdc79fe4dd591b1c0b861c3e01b6097f3</cites><orcidid>0000-0002-4216-2986</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00381-022-05520-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00381-022-05520-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27926,27927,41490,42559,51321</link.rule.ids></links><search><creatorcontrib>Alharbi, Shatha</creatorcontrib><creatorcontrib>Bawazir, Minyal</creatorcontrib><creatorcontrib>Altweijri, Ikhlass</creatorcontrib><title>A case of postoperative cerebellar mutism with hyperphagia in a child following gross total resection of medulloblastoma occupying the cerebellar vermis</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><description>Introduction
Cerebellar mutism syndrome is a well-known complication following posterior fossa tumor resection. Its incidence is markedly increased among patients with medulloblastoma. Patients typically present with an inability to communicate verbally due to disruption of the dentato-thalamocortical pathway.
Case Description
We present a unique case of cerebellar mutism in a three-year-old girl who underwent gross total resection of medulloblastoma occupying the cerebellar vermis. In addition to mutism, the patient developed hyperphagia.
Discussion
This case report aims to contribute to current understanding of the role of cerebello-hypothalamic connections in cerebellar mutism and their clinical significance.</description><subject>Case Report</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kb1OxDAQhC0EEsfBC1C5pAmsncRJyhPiT0KigdpynM3FpyQOtgO6N-FxcTgaGqptvpnZ0RByyeCaARQ3HiAtWQKcJ5DnHJLqiKxYlqYJpDkckxXwXCQFZHBKzrzfAbC85NWKfG2oVh6pbelkfbATOhXMB1KNDmvse-XoMAfjB_ppQke7fSSmTm2NomakiurO9A1tbd_bTzNu6dZZ72mwQfXUoUcdjB0X-wGbOUJ1r2LMoKjVep72iyR0f-I-0A3Gn5OTVvUeL37vmrzd373ePibPLw9Pt5vnRPM8C0mRQa2w1iwTLOUalWi0KLBsBG-R8bJudFG1mDVNXrGaaahLwXSKwGoBVdGma3J18J2cfZ_RBxnD9fLJiHb2kgvBqjxjwCLKD6heOjps5eTMoNxeMpDLDPIwg4wzyJ8ZZBVF6UHkIzxu0cmdnd0YK_2n-ga-S4-M</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Alharbi, Shatha</creator><creator>Bawazir, Minyal</creator><creator>Altweijri, Ikhlass</creator><general>Springer Berlin Heidelberg</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4216-2986</orcidid></search><sort><creationdate>20221101</creationdate><title>A case of postoperative cerebellar mutism with hyperphagia in a child following gross total resection of medulloblastoma occupying the cerebellar vermis</title><author>Alharbi, Shatha ; Bawazir, Minyal ; Altweijri, Ikhlass</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c254t-740baebc146132cea6dc67e8d62fe128bdc79fe4dd591b1c0b861c3e01b6097f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Case Report</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alharbi, Shatha</creatorcontrib><creatorcontrib>Bawazir, Minyal</creatorcontrib><creatorcontrib>Altweijri, Ikhlass</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alharbi, Shatha</au><au>Bawazir, Minyal</au><au>Altweijri, Ikhlass</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of postoperative cerebellar mutism with hyperphagia in a child following gross total resection of medulloblastoma occupying the cerebellar vermis</atitle><jtitle>Child's nervous system</jtitle><stitle>Childs Nerv Syst</stitle><date>2022-11-01</date><risdate>2022</risdate><volume>38</volume><issue>11</issue><spage>2189</spage><epage>2198</epage><pages>2189-2198</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Introduction
Cerebellar mutism syndrome is a well-known complication following posterior fossa tumor resection. Its incidence is markedly increased among patients with medulloblastoma. Patients typically present with an inability to communicate verbally due to disruption of the dentato-thalamocortical pathway.
Case Description
We present a unique case of cerebellar mutism in a three-year-old girl who underwent gross total resection of medulloblastoma occupying the cerebellar vermis. In addition to mutism, the patient developed hyperphagia.
Discussion
This case report aims to contribute to current understanding of the role of cerebello-hypothalamic connections in cerebellar mutism and their clinical significance.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00381-022-05520-9</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-4216-2986</orcidid></addata></record> |
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| source | SpringerNature Journals |
| subjects | Case Report Medicine Medicine & Public Health Neurosciences Neurosurgery |
| title | A case of postoperative cerebellar mutism with hyperphagia in a child following gross total resection of medulloblastoma occupying the cerebellar vermis |
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