Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition
Background Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring after injury to the dentato-rubro-olivary pathway (“Guillain-Mollaret triangle”). The majority of studies have described HOD resulting from posterior fossa (PF) hemorrhage or infarction. HOD in...
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Veröffentlicht in: | Child's nervous system 2018-03, Vol.34 (3), p.409-415 |
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description | Background
Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring after injury to the dentato-rubro-olivary pathway (“Guillain-Mollaret triangle”). The majority of studies have described HOD resulting from posterior fossa (PF) hemorrhage or infarction. HOD in patients undergoing PF surgery has not been well characterized. These lesions are rare and symptomatic children with HOD are even more uncommon. The purpose of this study was to evaluate HOD that develops after PF operations in children.
Materials and methods
A literature review was carried out describing 37 pediatric cases of HOD in 13 articles. In addition, two new cases of our own experience were included.
Conclusions
HOD is a rare complication related after PF tumors surgery and symptoms may be misdiagnosed with pediatric cerebellar mutism syndrome. Children with HOD usually do not develop palatal tremor but ataxia is common. |
doi_str_mv | 10.1007/s00381-017-3705-6 |
format | Article |
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Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring after injury to the dentato-rubro-olivary pathway (“Guillain-Mollaret triangle”). The majority of studies have described HOD resulting from posterior fossa (PF) hemorrhage or infarction. HOD in patients undergoing PF surgery has not been well characterized. These lesions are rare and symptomatic children with HOD are even more uncommon. The purpose of this study was to evaluate HOD that develops after PF operations in children.
Materials and methods
A literature review was carried out describing 37 pediatric cases of HOD in 13 articles. In addition, two new cases of our own experience were included.
Conclusions
HOD is a rare complication related after PF tumors surgery and symptoms may be misdiagnosed with pediatric cerebellar mutism syndrome. Children with HOD usually do not develop palatal tremor but ataxia is common.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-017-3705-6</identifier><identifier>PMID: 29279964</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Case-Based Update ; Cerebellar Neoplasms - diagnostic imaging ; Cerebellar Neoplasms - surgery ; Child ; Female ; Humans ; Hypertrophy - diagnostic imaging ; Hypertrophy - etiology ; Infratentorial Neoplasms - diagnostic imaging ; Infratentorial Neoplasms - surgery ; Male ; Medicine ; Medicine & Public Health ; Medulloblastoma - diagnostic imaging ; Medulloblastoma - surgery ; Neurodegenerative Diseases - diagnostic imaging ; Neurodegenerative Diseases - etiology ; Neurosciences ; Neurosurgery ; Olivary Nucleus - diagnostic imaging ; Postoperative Complications - diagnostic imaging ; Postoperative Complications - etiology</subject><ispartof>Child's nervous system, 2018-03, Vol.34 (3), p.409-415</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-e70dd10161f3a8dae3bf7df4e52a884ea3de3de2f14a85dc04e2dfadf6ec06cf3</citedby><cites>FETCH-LOGICAL-c344t-e70dd10161f3a8dae3bf7df4e52a884ea3de3de2f14a85dc04e2dfadf6ec06cf3</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/s00381-017-3705-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00381-017-3705-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29279964$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ballestero, Matheus Fernando Manzolli</creatorcontrib><creatorcontrib>Viana, Dinark Conceição</creatorcontrib><creatorcontrib>Teixeira, Thiago Lyrio</creatorcontrib><creatorcontrib>Santos, Marcelo Volpon</creatorcontrib><creatorcontrib>de Oliveira, Ricardo Santos</creatorcontrib><title>Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><addtitle>Childs Nerv Syst</addtitle><description>Background
Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring after injury to the dentato-rubro-olivary pathway (“Guillain-Mollaret triangle”). The majority of studies have described HOD resulting from posterior fossa (PF) hemorrhage or infarction. HOD in patients undergoing PF surgery has not been well characterized. These lesions are rare and symptomatic children with HOD are even more uncommon. The purpose of this study was to evaluate HOD that develops after PF operations in children.
Materials and methods
A literature review was carried out describing 37 pediatric cases of HOD in 13 articles. In addition, two new cases of our own experience were included.
Conclusions
HOD is a rare complication related after PF tumors surgery and symptoms may be misdiagnosed with pediatric cerebellar mutism syndrome. Children with HOD usually do not develop palatal tremor but ataxia is common.</description><subject>Adolescent</subject><subject>Case-Based Update</subject><subject>Cerebellar Neoplasms - diagnostic imaging</subject><subject>Cerebellar Neoplasms - surgery</subject><subject>Child</subject><subject>Female</subject><subject>Humans</subject><subject>Hypertrophy - diagnostic imaging</subject><subject>Hypertrophy - etiology</subject><subject>Infratentorial Neoplasms - diagnostic imaging</subject><subject>Infratentorial Neoplasms - surgery</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medulloblastoma - diagnostic imaging</subject><subject>Medulloblastoma - surgery</subject><subject>Neurodegenerative Diseases - diagnostic imaging</subject><subject>Neurodegenerative Diseases - etiology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Olivary Nucleus - diagnostic imaging</subject><subject>Postoperative Complications - diagnostic imaging</subject><subject>Postoperative Complications - etiology</subject><issn>0256-7040</issn><issn>1433-0350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLAzEUhYMoWh8_wI1k6Wb0ZpJ5LYuoFQpudB1ictNGpsmYzAj996a0uhQunMU958D5CLlmcMcAmvsEwFtWAGsK3kBV1EdkxgTnBfAKjskMyqouGhBwRs5T-gRgVVt2p-Ss7Mqm62oxI-vFdsA4xjCsnaahd98qbqnBFXqManTBU-epXrveRPRU2REjHULK4kKkNqSkaJriCuP2js49nbzBaJxa-ZDQUB28cbuaS3JiVZ_w6qAX5P3p8e1hUSxfn18e5stCcyHGAhswhgGrmeWqNQr5h22MFViVqm0FKm4wX2mZUG1lNAgsjVXG1qih1pZfkNt97xDD14RplBuXNPa98himJFnXMqi4qOpsZXurjnlGRCuH6DZ5v2Qgd4DlHrDMgOUOsNxlbg7108cGzV_il2g2lHtDyi-fscjPMEWfJ__T-gNem4no</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Ballestero, Matheus Fernando Manzolli</creator><creator>Viana, Dinark Conceição</creator><creator>Teixeira, Thiago Lyrio</creator><creator>Santos, Marcelo Volpon</creator><creator>de Oliveira, Ricardo Santos</creator><general>Springer Berlin Heidelberg</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>20180301</creationdate><title>Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition</title><author>Ballestero, Matheus Fernando Manzolli ; Viana, Dinark Conceição ; Teixeira, Thiago Lyrio ; Santos, Marcelo Volpon ; de Oliveira, Ricardo Santos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-e70dd10161f3a8dae3bf7df4e52a884ea3de3de2f14a85dc04e2dfadf6ec06cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adolescent</topic><topic>Case-Based Update</topic><topic>Cerebellar Neoplasms - diagnostic imaging</topic><topic>Cerebellar Neoplasms - surgery</topic><topic>Child</topic><topic>Female</topic><topic>Humans</topic><topic>Hypertrophy - diagnostic imaging</topic><topic>Hypertrophy - etiology</topic><topic>Infratentorial Neoplasms - diagnostic imaging</topic><topic>Infratentorial Neoplasms - surgery</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medulloblastoma - diagnostic imaging</topic><topic>Medulloblastoma - surgery</topic><topic>Neurodegenerative Diseases - diagnostic imaging</topic><topic>Neurodegenerative Diseases - etiology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Olivary Nucleus - diagnostic imaging</topic><topic>Postoperative Complications - diagnostic imaging</topic><topic>Postoperative Complications - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ballestero, Matheus Fernando Manzolli</creatorcontrib><creatorcontrib>Viana, Dinark Conceição</creatorcontrib><creatorcontrib>Teixeira, Thiago Lyrio</creatorcontrib><creatorcontrib>Santos, Marcelo Volpon</creatorcontrib><creatorcontrib>de Oliveira, Ricardo Santos</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>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ballestero, Matheus Fernando Manzolli</au><au>Viana, Dinark Conceição</au><au>Teixeira, Thiago Lyrio</au><au>Santos, Marcelo Volpon</au><au>de Oliveira, Ricardo Santos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition</atitle><jtitle>Child's nervous system</jtitle><stitle>Childs Nerv Syst</stitle><addtitle>Childs Nerv Syst</addtitle><date>2018-03-01</date><risdate>2018</risdate><volume>34</volume><issue>3</issue><spage>409</spage><epage>415</epage><pages>409-415</pages><issn>0256-7040</issn><eissn>1433-0350</eissn><abstract>Background
Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring after injury to the dentato-rubro-olivary pathway (“Guillain-Mollaret triangle”). The majority of studies have described HOD resulting from posterior fossa (PF) hemorrhage or infarction. HOD in patients undergoing PF surgery has not been well characterized. These lesions are rare and symptomatic children with HOD are even more uncommon. The purpose of this study was to evaluate HOD that develops after PF operations in children.
Materials and methods
A literature review was carried out describing 37 pediatric cases of HOD in 13 articles. In addition, two new cases of our own experience were included.
Conclusions
HOD is a rare complication related after PF tumors surgery and symptoms may be misdiagnosed with pediatric cerebellar mutism syndrome. Children with HOD usually do not develop palatal tremor but ataxia is common.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>29279964</pmid><doi>10.1007/s00381-017-3705-6</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Case-Based Update Cerebellar Neoplasms - diagnostic imaging Cerebellar Neoplasms - surgery Child Female Humans Hypertrophy - diagnostic imaging Hypertrophy - etiology Infratentorial Neoplasms - diagnostic imaging Infratentorial Neoplasms - surgery Male Medicine Medicine & Public Health Medulloblastoma - diagnostic imaging Medulloblastoma - surgery Neurodegenerative Diseases - diagnostic imaging Neurodegenerative Diseases - etiology Neurosciences Neurosurgery Olivary Nucleus - diagnostic imaging Postoperative Complications - diagnostic imaging Postoperative Complications - etiology |
title | Hypertrophic olivary degeneration in children after posterior fossa surgery. An underdiagnosed condition |
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