Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video

Radioinduced cavernous malformations (RICMs) are low-flow, angiographically occult vascular lesions. Giant radioinduced cavernous malformations (GRICMs) are a subtype of RICMs that are characterized by their large size. GRICMs are defined as RICMs that are larger than 3 cm in diameter.1 They are unc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:World neurosurgery 2024-04, Vol.184, p.42-43
Hauptverfasser: Finger, Guilherme, Zimelewicz Oberman, Dan, Loyola Godoy, Bruno, de Miranda Chaves Christiani, Marcio, Aversa, Antonio
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 43
container_issue
container_start_page 42
container_title World neurosurgery
container_volume 184
creator Finger, Guilherme
Zimelewicz Oberman, Dan
Loyola Godoy, Bruno
de Miranda Chaves Christiani, Marcio
Aversa, Antonio
description Radioinduced cavernous malformations (RICMs) are low-flow, angiographically occult vascular lesions. Giant radioinduced cavernous malformations (GRICMs) are a subtype of RICMs that are characterized by their large size. GRICMs are defined as RICMs that are larger than 3 cm in diameter.1 They are uncommon conditions accounting for 0.1% to 0.5% among patients who have received radiation therapy for head and neck cancer or brain tumors.2,3 The risk of developing GRICMs increases with the dose of radiation received and the length of time since radiation exposure.4 Other factors that may increase the risk of developing GRICMs include age, genetic predisposition, and underlying medical conditions.5 Due to the relatively low incidence of GRICMs and the limited number of studies on this condition, there are limited data about the management of this condition. This case report describes a 12-year-old female who was previously treated for a pilocytic astrocytoma in 2012. After undergoing stereotactic biopsy and whole-brain radiotherapy (50 gray in 28 sections), she was diagnosed with a radioinduced cavernous malformation in 2016 during follow-up imaging. The RICM was managed conservatively with imaging follow-up, which showed no increase in size between 2016 and 2019. However, in 2020, the patient experienced a seizure episode associated with left-sided hemiplegia. Further investigation with cranial magnetic resonance imaging and digital subtraction angiography showed a mixed-intensity image and surrounded by a low signal intensity rim on T2-weighted images, representing hemosiderin in the right central lobe, with intense perilesional edema, with no enhancement. Given the size and location of the mass, the patient underwent microsurgical resection of the RICM (Video 1). The surgery was successful, and the lesion was successfully resected. This case highlights the importance of careful monitoring for RICMs in patients who have received radiation therapy, as well as the potential for these lesions to cause significant symptoms and disability. The case also demonstrates that surgical intervention may be necessary in some cases to manage RICMs and that microsurgical resection can be an effective treatment option. The patient gave informed consent for surgery and video recording.
doi_str_mv 10.1016/j.wneu.2024.01.026
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2923327908</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1878875024000391</els_id><sourcerecordid>2923327908</sourcerecordid><originalsourceid>FETCH-LOGICAL-c307t-208c11fca2a0da5dcae1055964d20de698b19537b81a0a3af22e348467632ddd3</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMottT-AQ-yRy-75mM_suJFqtZCi1DUi4eQJrOSsrupSbfivzdLa4_mMhl45mXmQeiS4IRgkt-sk-8WuoRimiaYJJjmJ2hIeMFjXuTl6fGf4QEae7_G4TGS8oKdowHjlPA0JUP0sTDKWd-5T6NkHS3Bg9oa20a2iqZGtttoKbWx8azVnQIdTeQOXGs7Hy1kXVnXyJ6-jWgcPZgGWh-6kPNuNNgLdFbJ2sP4UEfo7enxdfIcz1-ms8n9PFYMF9uYYq4IqZSkEmuZaSWB4Cwr81RTrCEv-YqUGStWnEgsmawoBZbyNC9yRrXWbISu97kbZ7868FvRGK-grmULYVNBS8oYLUrMA0r3aH-0d1CJjTONdD-CYNF7FWvRexW9V4GJCF7D0NUhv1s1oI8jfxYDcLcHIFy5M-CEVwba4Mu4oFNoa_7L_wXlTYj0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2923327908</pqid></control><display><type>article</type><title>Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video</title><source>Access via ScienceDirect (Elsevier)</source><creator>Finger, Guilherme ; Zimelewicz Oberman, Dan ; Loyola Godoy, Bruno ; de Miranda Chaves Christiani, Marcio ; Aversa, Antonio</creator><creatorcontrib>Finger, Guilherme ; Zimelewicz Oberman, Dan ; Loyola Godoy, Bruno ; de Miranda Chaves Christiani, Marcio ; Aversa, Antonio</creatorcontrib><description>Radioinduced cavernous malformations (RICMs) are low-flow, angiographically occult vascular lesions. Giant radioinduced cavernous malformations (GRICMs) are a subtype of RICMs that are characterized by their large size. GRICMs are defined as RICMs that are larger than 3 cm in diameter.1 They are uncommon conditions accounting for 0.1% to 0.5% among patients who have received radiation therapy for head and neck cancer or brain tumors.2,3 The risk of developing GRICMs increases with the dose of radiation received and the length of time since radiation exposure.4 Other factors that may increase the risk of developing GRICMs include age, genetic predisposition, and underlying medical conditions.5 Due to the relatively low incidence of GRICMs and the limited number of studies on this condition, there are limited data about the management of this condition. This case report describes a 12-year-old female who was previously treated for a pilocytic astrocytoma in 2012. After undergoing stereotactic biopsy and whole-brain radiotherapy (50 gray in 28 sections), she was diagnosed with a radioinduced cavernous malformation in 2016 during follow-up imaging. The RICM was managed conservatively with imaging follow-up, which showed no increase in size between 2016 and 2019. However, in 2020, the patient experienced a seizure episode associated with left-sided hemiplegia. Further investigation with cranial magnetic resonance imaging and digital subtraction angiography showed a mixed-intensity image and surrounded by a low signal intensity rim on T2-weighted images, representing hemosiderin in the right central lobe, with intense perilesional edema, with no enhancement. Given the size and location of the mass, the patient underwent microsurgical resection of the RICM (Video 1). The surgery was successful, and the lesion was successfully resected. This case highlights the importance of careful monitoring for RICMs in patients who have received radiation therapy, as well as the potential for these lesions to cause significant symptoms and disability. The case also demonstrates that surgical intervention may be necessary in some cases to manage RICMs and that microsurgical resection can be an effective treatment option. The patient gave informed consent for surgery and video recording.</description><identifier>ISSN: 1878-8750</identifier><identifier>ISSN: 1878-8769</identifier><identifier>EISSN: 1878-8769</identifier><identifier>DOI: 10.1016/j.wneu.2024.01.026</identifier><identifier>PMID: 38218441</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cavernous malformation ; Management ; Radio-induced</subject><ispartof>World neurosurgery, 2024-04, Vol.184, p.42-43</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c307t-208c11fca2a0da5dcae1055964d20de698b19537b81a0a3af22e348467632ddd3</cites><orcidid>0000-0003-0827-1254 ; 0000-0001-8964-4328</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.wneu.2024.01.026$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38218441$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Finger, Guilherme</creatorcontrib><creatorcontrib>Zimelewicz Oberman, Dan</creatorcontrib><creatorcontrib>Loyola Godoy, Bruno</creatorcontrib><creatorcontrib>de Miranda Chaves Christiani, Marcio</creatorcontrib><creatorcontrib>Aversa, Antonio</creatorcontrib><title>Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video</title><title>World neurosurgery</title><addtitle>World Neurosurg</addtitle><description>Radioinduced cavernous malformations (RICMs) are low-flow, angiographically occult vascular lesions. Giant radioinduced cavernous malformations (GRICMs) are a subtype of RICMs that are characterized by their large size. GRICMs are defined as RICMs that are larger than 3 cm in diameter.1 They are uncommon conditions accounting for 0.1% to 0.5% among patients who have received radiation therapy for head and neck cancer or brain tumors.2,3 The risk of developing GRICMs increases with the dose of radiation received and the length of time since radiation exposure.4 Other factors that may increase the risk of developing GRICMs include age, genetic predisposition, and underlying medical conditions.5 Due to the relatively low incidence of GRICMs and the limited number of studies on this condition, there are limited data about the management of this condition. This case report describes a 12-year-old female who was previously treated for a pilocytic astrocytoma in 2012. After undergoing stereotactic biopsy and whole-brain radiotherapy (50 gray in 28 sections), she was diagnosed with a radioinduced cavernous malformation in 2016 during follow-up imaging. The RICM was managed conservatively with imaging follow-up, which showed no increase in size between 2016 and 2019. However, in 2020, the patient experienced a seizure episode associated with left-sided hemiplegia. Further investigation with cranial magnetic resonance imaging and digital subtraction angiography showed a mixed-intensity image and surrounded by a low signal intensity rim on T2-weighted images, representing hemosiderin in the right central lobe, with intense perilesional edema, with no enhancement. Given the size and location of the mass, the patient underwent microsurgical resection of the RICM (Video 1). The surgery was successful, and the lesion was successfully resected. This case highlights the importance of careful monitoring for RICMs in patients who have received radiation therapy, as well as the potential for these lesions to cause significant symptoms and disability. The case also demonstrates that surgical intervention may be necessary in some cases to manage RICMs and that microsurgical resection can be an effective treatment option. The patient gave informed consent for surgery and video recording.</description><subject>Cavernous malformation</subject><subject>Management</subject><subject>Radio-induced</subject><issn>1878-8750</issn><issn>1878-8769</issn><issn>1878-8769</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMottT-AQ-yRy-75mM_suJFqtZCi1DUi4eQJrOSsrupSbfivzdLa4_mMhl45mXmQeiS4IRgkt-sk-8WuoRimiaYJJjmJ2hIeMFjXuTl6fGf4QEae7_G4TGS8oKdowHjlPA0JUP0sTDKWd-5T6NkHS3Bg9oa20a2iqZGtttoKbWx8azVnQIdTeQOXGs7Hy1kXVnXyJ6-jWgcPZgGWh-6kPNuNNgLdFbJ2sP4UEfo7enxdfIcz1-ms8n9PFYMF9uYYq4IqZSkEmuZaSWB4Cwr81RTrCEv-YqUGStWnEgsmawoBZbyNC9yRrXWbISu97kbZ7868FvRGK-grmULYVNBS8oYLUrMA0r3aH-0d1CJjTONdD-CYNF7FWvRexW9V4GJCF7D0NUhv1s1oI8jfxYDcLcHIFy5M-CEVwba4Mu4oFNoa_7L_wXlTYj0</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Finger, Guilherme</creator><creator>Zimelewicz Oberman, Dan</creator><creator>Loyola Godoy, Bruno</creator><creator>de Miranda Chaves Christiani, Marcio</creator><creator>Aversa, Antonio</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0827-1254</orcidid><orcidid>https://orcid.org/0000-0001-8964-4328</orcidid></search><sort><creationdate>202404</creationdate><title>Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video</title><author>Finger, Guilherme ; Zimelewicz Oberman, Dan ; Loyola Godoy, Bruno ; de Miranda Chaves Christiani, Marcio ; Aversa, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-208c11fca2a0da5dcae1055964d20de698b19537b81a0a3af22e348467632ddd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Cavernous malformation</topic><topic>Management</topic><topic>Radio-induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Finger, Guilherme</creatorcontrib><creatorcontrib>Zimelewicz Oberman, Dan</creatorcontrib><creatorcontrib>Loyola Godoy, Bruno</creatorcontrib><creatorcontrib>de Miranda Chaves Christiani, Marcio</creatorcontrib><creatorcontrib>Aversa, Antonio</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>World neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Finger, Guilherme</au><au>Zimelewicz Oberman, Dan</au><au>Loyola Godoy, Bruno</au><au>de Miranda Chaves Christiani, Marcio</au><au>Aversa, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video</atitle><jtitle>World neurosurgery</jtitle><addtitle>World Neurosurg</addtitle><date>2024-04</date><risdate>2024</risdate><volume>184</volume><spage>42</spage><epage>43</epage><pages>42-43</pages><issn>1878-8750</issn><issn>1878-8769</issn><eissn>1878-8769</eissn><abstract>Radioinduced cavernous malformations (RICMs) are low-flow, angiographically occult vascular lesions. Giant radioinduced cavernous malformations (GRICMs) are a subtype of RICMs that are characterized by their large size. GRICMs are defined as RICMs that are larger than 3 cm in diameter.1 They are uncommon conditions accounting for 0.1% to 0.5% among patients who have received radiation therapy for head and neck cancer or brain tumors.2,3 The risk of developing GRICMs increases with the dose of radiation received and the length of time since radiation exposure.4 Other factors that may increase the risk of developing GRICMs include age, genetic predisposition, and underlying medical conditions.5 Due to the relatively low incidence of GRICMs and the limited number of studies on this condition, there are limited data about the management of this condition. This case report describes a 12-year-old female who was previously treated for a pilocytic astrocytoma in 2012. After undergoing stereotactic biopsy and whole-brain radiotherapy (50 gray in 28 sections), she was diagnosed with a radioinduced cavernous malformation in 2016 during follow-up imaging. The RICM was managed conservatively with imaging follow-up, which showed no increase in size between 2016 and 2019. However, in 2020, the patient experienced a seizure episode associated with left-sided hemiplegia. Further investigation with cranial magnetic resonance imaging and digital subtraction angiography showed a mixed-intensity image and surrounded by a low signal intensity rim on T2-weighted images, representing hemosiderin in the right central lobe, with intense perilesional edema, with no enhancement. Given the size and location of the mass, the patient underwent microsurgical resection of the RICM (Video 1). The surgery was successful, and the lesion was successfully resected. This case highlights the importance of careful monitoring for RICMs in patients who have received radiation therapy, as well as the potential for these lesions to cause significant symptoms and disability. The case also demonstrates that surgical intervention may be necessary in some cases to manage RICMs and that microsurgical resection can be an effective treatment option. The patient gave informed consent for surgery and video recording.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38218441</pmid><doi>10.1016/j.wneu.2024.01.026</doi><tpages>2</tpages><orcidid>https://orcid.org/0000-0003-0827-1254</orcidid><orcidid>https://orcid.org/0000-0001-8964-4328</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1878-8750
ispartof World neurosurgery, 2024-04, Vol.184, p.42-43
issn 1878-8750
1878-8769
1878-8769
language eng
recordid cdi_proquest_miscellaneous_2923327908
source Access via ScienceDirect (Elsevier)
subjects Cavernous malformation
Management
Radio-induced
title Microsurgical Resection of Giant Radio-Induced Cavernous Malformation: 2- Dimensional Video
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T15%3A19%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Microsurgical%20Resection%20of%20Giant%20Radio-Induced%20Cavernous%20Malformation:%202-%20Dimensional%20Video&rft.jtitle=World%20neurosurgery&rft.au=Finger,%20Guilherme&rft.date=2024-04&rft.volume=184&rft.spage=42&rft.epage=43&rft.pages=42-43&rft.issn=1878-8750&rft.eissn=1878-8769&rft_id=info:doi/10.1016/j.wneu.2024.01.026&rft_dat=%3Cproquest_cross%3E2923327908%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2923327908&rft_id=info:pmid/38218441&rft_els_id=S1878875024000391&rfr_iscdi=true