Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review
Background Eagle jugular syndrome (EJS), recently identified as a cause of cerebrovascular disease (CVD) due to venous obstruction by an elongated styloid process (SP), is reported here alongside a case of concurrent de novo cerebral cavernous malformation (CCM). This study aims to explore the poten...
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description | Background
Eagle jugular syndrome (EJS), recently identified as a cause of cerebrovascular disease (CVD) due to venous obstruction by an elongated styloid process (SP), is reported here alongside a case of concurrent de novo cerebral cavernous malformation (CCM). This study aims to explore the potential causal relationship between EJS and de novo CCM through a comprehensive literature review.
Method
Systematic literature reviews, spanning from 1995 to 2023, focused on EJS cases with definitive signs and symptoms and de novo CCM cases with detailed clinical characteristics. Data on the pathophysiology and clinical manifestations of EJS, as well as potential risk factors preceding de novo CCM, were collected to assess the relationship between the two conditions.
Result
Among 14 patients from 11 articles on EJS, the most common presentation was increased intracranial hypertension (IIH), observed in 10 patients (71.4%), followed by dural sinus thrombosis in four patients (28.6%). In contrast, 30 patients from 28 articles were identified with de novo CCM, involving 37 lesions. In these cases, 13 patients developed CCM subsequent to developmental venous anomalies (43%), seven following dural arteriovenous fistula (dAVF) (23%), and two after sinus thrombosis (6%). In a specific case of de novo brainstem CCM, the development of an enlarged condylar emissary vein, indicative of venous congestion due to IJV compression by the elongated SP, was noted before the emergence of CCM.
Conclusion
This study underscores that venous congestion, a primary result of symptomatic EJS, might lead to the development of de novo CCM. Thus, EJS could potentially be an indicator of CCM development. Further epidemiological and pathophysiological investigations focusing on venous circulation are necessary to clarify the causal relationship between EJS and CCM. |
doi_str_mv | 10.1007/s00701-024-05900-x |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2915989138</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2915780560</sourcerecordid><originalsourceid>FETCH-LOGICAL-c326t-4a49029758bc8c245ef771ab6b20904c645b289b2e3e1fe18ee3a762c53cb033</originalsourceid><addsrcrecordid>eNp9kUtPAyEUhYnR-Kj-AReGxI2b0QvMC3fG-EpM3HRPgLnTTDMDFTrV_nvR-ooLNweS893DDYeQYwbnDKC6iEmAZcDzDAoJkL1ukX2QOc-SwPav-x45iHEOwHiVi12yJ2oumAC-T9yNnvVI5-Ns7HWgce2a4Aek2lo_LLTrsKFmTRukzq88NUF3Li5xoFavMDg_RjrovvVh0MvOu0uqkxMxM0maFPfOJsfSgKsOXw7JTqv7iEef54RMb2-m1_fZ49Pdw_XVY2YFL5dZrnMJXFZFbWxteV5gW1VMm9JwkJDbMi8Mr6XhKJC1yGpEoauS20JYA0JMyNkmdhH884hxqYYuWux77TCtrLhkhawlE3VCT_-gcz8Gl5b7oKoaihISxTeUDT7GgK1ahG7QYa0YqPcy1KYMlcpQH2Wo1zR08hk9mgGb75Gv30-A2AAxWW6G4eftf2LfAFAFlec</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2915780560</pqid></control><display><type>article</type><title>Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review</title><source>SpringerNature Journals</source><creator>Motoyama, Yasushi ; Sasaki, Hiromitsu ; Nakajima, Tsukasa ; Hayami, Hiromichi ; Matsuoka, Ryuta ; Fukutome, Kenji ; Tei, Rinsei ; Shin, Yasushi ; Aketa, Shuta</creator><creatorcontrib>Motoyama, Yasushi ; Sasaki, Hiromitsu ; Nakajima, Tsukasa ; Hayami, Hiromichi ; Matsuoka, Ryuta ; Fukutome, Kenji ; Tei, Rinsei ; Shin, Yasushi ; Aketa, Shuta</creatorcontrib><description>Background
Eagle jugular syndrome (EJS), recently identified as a cause of cerebrovascular disease (CVD) due to venous obstruction by an elongated styloid process (SP), is reported here alongside a case of concurrent de novo cerebral cavernous malformation (CCM). This study aims to explore the potential causal relationship between EJS and de novo CCM through a comprehensive literature review.
Method
Systematic literature reviews, spanning from 1995 to 2023, focused on EJS cases with definitive signs and symptoms and de novo CCM cases with detailed clinical characteristics. Data on the pathophysiology and clinical manifestations of EJS, as well as potential risk factors preceding de novo CCM, were collected to assess the relationship between the two conditions.
Result
Among 14 patients from 11 articles on EJS, the most common presentation was increased intracranial hypertension (IIH), observed in 10 patients (71.4%), followed by dural sinus thrombosis in four patients (28.6%). In contrast, 30 patients from 28 articles were identified with de novo CCM, involving 37 lesions. In these cases, 13 patients developed CCM subsequent to developmental venous anomalies (43%), seven following dural arteriovenous fistula (dAVF) (23%), and two after sinus thrombosis (6%). In a specific case of de novo brainstem CCM, the development of an enlarged condylar emissary vein, indicative of venous congestion due to IJV compression by the elongated SP, was noted before the emergence of CCM.
Conclusion
This study underscores that venous congestion, a primary result of symptomatic EJS, might lead to the development of de novo CCM. Thus, EJS could potentially be an indicator of CCM development. Further epidemiological and pathophysiological investigations focusing on venous circulation are necessary to clarify the causal relationship between EJS and CCM.</description><identifier>ISSN: 0942-0940</identifier><identifier>ISSN: 0001-6268</identifier><identifier>EISSN: 0942-0940</identifier><identifier>DOI: 10.1007/s00701-024-05900-x</identifier><identifier>PMID: 38231302</identifier><language>eng</language><publisher>Vienna: Springer Vienna</publisher><subject>Brain stem ; Cerebrovascular diseases ; Epidemiology ; Interventional Radiology ; Literature reviews ; Medicine ; Medicine & Public Health ; Minimally Invasive Surgery ; Neurology ; Neuroradiology ; Neurosurgery ; Review Article ; Risk factors ; Surgical Orthopedics ; Thrombosis ; Vascular Neurosurgery – Other</subject><ispartof>Acta neurochirurgica, 2024-01, Vol.166 (1), p.20-20, Article 20</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-4a49029758bc8c245ef771ab6b20904c645b289b2e3e1fe18ee3a762c53cb033</cites><orcidid>0000-0003-1957-2124</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/s00701-024-05900-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00701-024-05900-x$$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/38231302$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Motoyama, Yasushi</creatorcontrib><creatorcontrib>Sasaki, Hiromitsu</creatorcontrib><creatorcontrib>Nakajima, Tsukasa</creatorcontrib><creatorcontrib>Hayami, Hiromichi</creatorcontrib><creatorcontrib>Matsuoka, Ryuta</creatorcontrib><creatorcontrib>Fukutome, Kenji</creatorcontrib><creatorcontrib>Tei, Rinsei</creatorcontrib><creatorcontrib>Shin, Yasushi</creatorcontrib><creatorcontrib>Aketa, Shuta</creatorcontrib><title>Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review</title><title>Acta neurochirurgica</title><addtitle>Acta Neurochir</addtitle><addtitle>Acta Neurochir (Wien)</addtitle><description>Background
Eagle jugular syndrome (EJS), recently identified as a cause of cerebrovascular disease (CVD) due to venous obstruction by an elongated styloid process (SP), is reported here alongside a case of concurrent de novo cerebral cavernous malformation (CCM). This study aims to explore the potential causal relationship between EJS and de novo CCM through a comprehensive literature review.
Method
Systematic literature reviews, spanning from 1995 to 2023, focused on EJS cases with definitive signs and symptoms and de novo CCM cases with detailed clinical characteristics. Data on the pathophysiology and clinical manifestations of EJS, as well as potential risk factors preceding de novo CCM, were collected to assess the relationship between the two conditions.
Result
Among 14 patients from 11 articles on EJS, the most common presentation was increased intracranial hypertension (IIH), observed in 10 patients (71.4%), followed by dural sinus thrombosis in four patients (28.6%). In contrast, 30 patients from 28 articles were identified with de novo CCM, involving 37 lesions. In these cases, 13 patients developed CCM subsequent to developmental venous anomalies (43%), seven following dural arteriovenous fistula (dAVF) (23%), and two after sinus thrombosis (6%). In a specific case of de novo brainstem CCM, the development of an enlarged condylar emissary vein, indicative of venous congestion due to IJV compression by the elongated SP, was noted before the emergence of CCM.
Conclusion
This study underscores that venous congestion, a primary result of symptomatic EJS, might lead to the development of de novo CCM. Thus, EJS could potentially be an indicator of CCM development. Further epidemiological and pathophysiological investigations focusing on venous circulation are necessary to clarify the causal relationship between EJS and CCM.</description><subject>Brain stem</subject><subject>Cerebrovascular diseases</subject><subject>Epidemiology</subject><subject>Interventional Radiology</subject><subject>Literature reviews</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Minimally Invasive Surgery</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosurgery</subject><subject>Review Article</subject><subject>Risk factors</subject><subject>Surgical Orthopedics</subject><subject>Thrombosis</subject><subject>Vascular Neurosurgery – Other</subject><issn>0942-0940</issn><issn>0001-6268</issn><issn>0942-0940</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtPAyEUhYnR-Kj-AReGxI2b0QvMC3fG-EpM3HRPgLnTTDMDFTrV_nvR-ooLNweS893DDYeQYwbnDKC6iEmAZcDzDAoJkL1ukX2QOc-SwPav-x45iHEOwHiVi12yJ2oumAC-T9yNnvVI5-Ns7HWgce2a4Aek2lo_LLTrsKFmTRukzq88NUF3Li5xoFavMDg_RjrovvVh0MvOu0uqkxMxM0maFPfOJsfSgKsOXw7JTqv7iEef54RMb2-m1_fZ49Pdw_XVY2YFL5dZrnMJXFZFbWxteV5gW1VMm9JwkJDbMi8Mr6XhKJC1yGpEoauS20JYA0JMyNkmdhH884hxqYYuWux77TCtrLhkhawlE3VCT_-gcz8Gl5b7oKoaihISxTeUDT7GgK1ahG7QYa0YqPcy1KYMlcpQH2Wo1zR08hk9mgGb75Gv30-A2AAxWW6G4eftf2LfAFAFlec</recordid><startdate>20240117</startdate><enddate>20240117</enddate><creator>Motoyama, Yasushi</creator><creator>Sasaki, Hiromitsu</creator><creator>Nakajima, Tsukasa</creator><creator>Hayami, Hiromichi</creator><creator>Matsuoka, Ryuta</creator><creator>Fukutome, Kenji</creator><creator>Tei, Rinsei</creator><creator>Shin, Yasushi</creator><creator>Aketa, Shuta</creator><general>Springer Vienna</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1957-2124</orcidid></search><sort><creationdate>20240117</creationdate><title>Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review</title><author>Motoyama, Yasushi ; Sasaki, Hiromitsu ; Nakajima, Tsukasa ; Hayami, Hiromichi ; Matsuoka, Ryuta ; Fukutome, Kenji ; Tei, Rinsei ; Shin, Yasushi ; Aketa, Shuta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-4a49029758bc8c245ef771ab6b20904c645b289b2e3e1fe18ee3a762c53cb033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Brain stem</topic><topic>Cerebrovascular diseases</topic><topic>Epidemiology</topic><topic>Interventional Radiology</topic><topic>Literature reviews</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Minimally Invasive Surgery</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosurgery</topic><topic>Review Article</topic><topic>Risk factors</topic><topic>Surgical Orthopedics</topic><topic>Thrombosis</topic><topic>Vascular Neurosurgery – Other</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Motoyama, Yasushi</creatorcontrib><creatorcontrib>Sasaki, Hiromitsu</creatorcontrib><creatorcontrib>Nakajima, Tsukasa</creatorcontrib><creatorcontrib>Hayami, Hiromichi</creatorcontrib><creatorcontrib>Matsuoka, Ryuta</creatorcontrib><creatorcontrib>Fukutome, Kenji</creatorcontrib><creatorcontrib>Tei, Rinsei</creatorcontrib><creatorcontrib>Shin, Yasushi</creatorcontrib><creatorcontrib>Aketa, Shuta</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neurochirurgica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Motoyama, Yasushi</au><au>Sasaki, Hiromitsu</au><au>Nakajima, Tsukasa</au><au>Hayami, Hiromichi</au><au>Matsuoka, Ryuta</au><au>Fukutome, Kenji</au><au>Tei, Rinsei</au><au>Shin, Yasushi</au><au>Aketa, Shuta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review</atitle><jtitle>Acta neurochirurgica</jtitle><stitle>Acta Neurochir</stitle><addtitle>Acta Neurochir (Wien)</addtitle><date>2024-01-17</date><risdate>2024</risdate><volume>166</volume><issue>1</issue><spage>20</spage><epage>20</epage><pages>20-20</pages><artnum>20</artnum><issn>0942-0940</issn><issn>0001-6268</issn><eissn>0942-0940</eissn><abstract>Background
Eagle jugular syndrome (EJS), recently identified as a cause of cerebrovascular disease (CVD) due to venous obstruction by an elongated styloid process (SP), is reported here alongside a case of concurrent de novo cerebral cavernous malformation (CCM). This study aims to explore the potential causal relationship between EJS and de novo CCM through a comprehensive literature review.
Method
Systematic literature reviews, spanning from 1995 to 2023, focused on EJS cases with definitive signs and symptoms and de novo CCM cases with detailed clinical characteristics. Data on the pathophysiology and clinical manifestations of EJS, as well as potential risk factors preceding de novo CCM, were collected to assess the relationship between the two conditions.
Result
Among 14 patients from 11 articles on EJS, the most common presentation was increased intracranial hypertension (IIH), observed in 10 patients (71.4%), followed by dural sinus thrombosis in four patients (28.6%). In contrast, 30 patients from 28 articles were identified with de novo CCM, involving 37 lesions. In these cases, 13 patients developed CCM subsequent to developmental venous anomalies (43%), seven following dural arteriovenous fistula (dAVF) (23%), and two after sinus thrombosis (6%). In a specific case of de novo brainstem CCM, the development of an enlarged condylar emissary vein, indicative of venous congestion due to IJV compression by the elongated SP, was noted before the emergence of CCM.
Conclusion
This study underscores that venous congestion, a primary result of symptomatic EJS, might lead to the development of de novo CCM. Thus, EJS could potentially be an indicator of CCM development. Further epidemiological and pathophysiological investigations focusing on venous circulation are necessary to clarify the causal relationship between EJS and CCM.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>38231302</pmid><doi>10.1007/s00701-024-05900-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1957-2124</orcidid></addata></record> |
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subjects | Brain stem Cerebrovascular diseases Epidemiology Interventional Radiology Literature reviews Medicine Medicine & Public Health Minimally Invasive Surgery Neurology Neuroradiology Neurosurgery Review Article Risk factors Surgical Orthopedics Thrombosis Vascular Neurosurgery – Other |
title | Eagle jugular syndrome accompanied by de novo brainstem cavernous malformation: a case-based systematic review |
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