Cavernous Malformations of the Brainstem Presenting in Childhood: Surgical Experience in 40 Patients
Abstract BACKGROUND: Brainstem cavernous malformations (BSCMs) are believed to compose 9% to 35% of all cerebral cavernous malformations, but these lesions have been reported in children in very limited numbers. OBJECTIVE: To review surgical outcomes of pediatric patients with BSCMs treated at 1 ins...
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Veröffentlicht in: | Neurosurgery 2010-12, Vol.67 (6), p.1589-1599 |
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creator | Abla, Adib A Lekovic, Gregory P Garrett, Mark Wilson, David A Nakaji, Peter Bristol, Ruth Spetzler, Robert F |
description | Abstract
BACKGROUND:
Brainstem cavernous malformations (BSCMs) are believed to compose 9% to 35% of all cerebral cavernous malformations, but these lesions have been reported in children in very limited numbers.
OBJECTIVE:
To review surgical outcomes of pediatric patients with BSCMs treated at 1 institution.
METHODS:
We retrospectively analyzed the course of 40 pediatric patients (19 males, 21 females; age range, 10 months to 18.9 years; mean, 12.3 years) who underwent surgery between 1984 and 2009. Age, sex, presenting symptoms, location of lesion, surgical approach, new postoperative deficits, Glasgow Outcome Scale score, recurrences, and resolution of baseline symptoms were recorded.
RESULTS:
Thirty-nine patients experienced hemorrhage before surgery. Lesion locations included the pons (n = 22), midbrain (n = 4), midbrain and thalamus (n = 4), pontomesencephalic junction (n = 3), medulla (n = 3), pontomedullary junction (n = 3), and cervicomedullary junction (n = 1). Mean lesion size was 2.3 cm. Mean length of hospital stay was 10.7 days. The average clinical follow-up was 31.9 months in 36 patients with follow-up after discharge. At last follow-up, 5 patients had experienced symptoms and/or imaging consistent with rehemorrhage, either from a residual that enlarged or true recurrence (5.25% annual rebleed risk per patient after surgery); 2 required reoperation for further resection of cavernoma. Mean Glasgow Outcome Scale score was 4.2 on admission, 4.05 at discharge, and 4.5 at latest follow-up. Preoperative symptoms and deficits improved in 16 patients (40%). New neurological deficits developed in 19 patients (48%) and resolved in 9, leaving 10 patients (25%) with new permanent deficit.
CONCLUSION:
Compared with adults, pediatric patients with BCSMs tend to have larger lesions and higher rates of recurrence (regrowth of residual lesion). Given the greater life expectancy of children, surgical treatment seems warranted in those with surgically accessible lesions that have bled. Outcomes were similar to those in our adult series of patients with BSCMs. |
doi_str_mv | 10.1227/NEU.0b013e3181f8d1b2 |
format | Article |
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BACKGROUND:
Brainstem cavernous malformations (BSCMs) are believed to compose 9% to 35% of all cerebral cavernous malformations, but these lesions have been reported in children in very limited numbers.
OBJECTIVE:
To review surgical outcomes of pediatric patients with BSCMs treated at 1 institution.
METHODS:
We retrospectively analyzed the course of 40 pediatric patients (19 males, 21 females; age range, 10 months to 18.9 years; mean, 12.3 years) who underwent surgery between 1984 and 2009. Age, sex, presenting symptoms, location of lesion, surgical approach, new postoperative deficits, Glasgow Outcome Scale score, recurrences, and resolution of baseline symptoms were recorded.
RESULTS:
Thirty-nine patients experienced hemorrhage before surgery. Lesion locations included the pons (n = 22), midbrain (n = 4), midbrain and thalamus (n = 4), pontomesencephalic junction (n = 3), medulla (n = 3), pontomedullary junction (n = 3), and cervicomedullary junction (n = 1). Mean lesion size was 2.3 cm. Mean length of hospital stay was 10.7 days. The average clinical follow-up was 31.9 months in 36 patients with follow-up after discharge. At last follow-up, 5 patients had experienced symptoms and/or imaging consistent with rehemorrhage, either from a residual that enlarged or true recurrence (5.25% annual rebleed risk per patient after surgery); 2 required reoperation for further resection of cavernoma. Mean Glasgow Outcome Scale score was 4.2 on admission, 4.05 at discharge, and 4.5 at latest follow-up. Preoperative symptoms and deficits improved in 16 patients (40%). New neurological deficits developed in 19 patients (48%) and resolved in 9, leaving 10 patients (25%) with new permanent deficit.
CONCLUSION:
Compared with adults, pediatric patients with BCSMs tend to have larger lesions and higher rates of recurrence (regrowth of residual lesion). Given the greater life expectancy of children, surgical treatment seems warranted in those with surgically accessible lesions that have bled. Outcomes were similar to those in our adult series of patients with BSCMs.</description><identifier>ISSN: 0148-396X</identifier><identifier>EISSN: 1524-4040</identifier><identifier>DOI: 10.1227/NEU.0b013e3181f8d1b2</identifier><identifier>PMID: 21107189</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adolescent ; Brain Stem - pathology ; Brain Stem - surgery ; Central Nervous System Vascular Malformations - pathology ; Central Nervous System Vascular Malformations - surgery ; Child ; Child, Preschool ; Childhood ; Female ; Follow-Up Studies ; Humans ; Infant ; Magnetic Resonance Imaging ; Male ; Neurosurgery - methods ; Pediatrics ; Retrospective Studies ; Surgery ; Surgical outcomes ; Treatment Outcome</subject><ispartof>Neurosurgery, 2010-12, Vol.67 (6), p.1589-1599</ispartof><rights>Copyright © 2010 by the Congress of Neurological Surgeons</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-585332cd84139af22d9bb245a2a0feca9885b7e0cb0ee7565bd43641614822213</citedby><cites>FETCH-LOGICAL-c440t-585332cd84139af22d9bb245a2a0feca9885b7e0cb0ee7565bd43641614822213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21107189$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abla, Adib A</creatorcontrib><creatorcontrib>Lekovic, Gregory P</creatorcontrib><creatorcontrib>Garrett, Mark</creatorcontrib><creatorcontrib>Wilson, David A</creatorcontrib><creatorcontrib>Nakaji, Peter</creatorcontrib><creatorcontrib>Bristol, Ruth</creatorcontrib><creatorcontrib>Spetzler, Robert F</creatorcontrib><title>Cavernous Malformations of the Brainstem Presenting in Childhood: Surgical Experience in 40 Patients</title><title>Neurosurgery</title><addtitle>Neurosurgery</addtitle><description>Abstract
BACKGROUND:
Brainstem cavernous malformations (BSCMs) are believed to compose 9% to 35% of all cerebral cavernous malformations, but these lesions have been reported in children in very limited numbers.
OBJECTIVE:
To review surgical outcomes of pediatric patients with BSCMs treated at 1 institution.
METHODS:
We retrospectively analyzed the course of 40 pediatric patients (19 males, 21 females; age range, 10 months to 18.9 years; mean, 12.3 years) who underwent surgery between 1984 and 2009. Age, sex, presenting symptoms, location of lesion, surgical approach, new postoperative deficits, Glasgow Outcome Scale score, recurrences, and resolution of baseline symptoms were recorded.
RESULTS:
Thirty-nine patients experienced hemorrhage before surgery. Lesion locations included the pons (n = 22), midbrain (n = 4), midbrain and thalamus (n = 4), pontomesencephalic junction (n = 3), medulla (n = 3), pontomedullary junction (n = 3), and cervicomedullary junction (n = 1). Mean lesion size was 2.3 cm. Mean length of hospital stay was 10.7 days. The average clinical follow-up was 31.9 months in 36 patients with follow-up after discharge. At last follow-up, 5 patients had experienced symptoms and/or imaging consistent with rehemorrhage, either from a residual that enlarged or true recurrence (5.25% annual rebleed risk per patient after surgery); 2 required reoperation for further resection of cavernoma. Mean Glasgow Outcome Scale score was 4.2 on admission, 4.05 at discharge, and 4.5 at latest follow-up. Preoperative symptoms and deficits improved in 16 patients (40%). New neurological deficits developed in 19 patients (48%) and resolved in 9, leaving 10 patients (25%) with new permanent deficit.
CONCLUSION:
Compared with adults, pediatric patients with BCSMs tend to have larger lesions and higher rates of recurrence (regrowth of residual lesion). Given the greater life expectancy of children, surgical treatment seems warranted in those with surgically accessible lesions that have bled. Outcomes were similar to those in our adult series of patients with BSCMs.</description><subject>Adolescent</subject><subject>Brain Stem - pathology</subject><subject>Brain Stem - surgery</subject><subject>Central Nervous System Vascular Malformations - pathology</subject><subject>Central Nervous System Vascular Malformations - surgery</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Childhood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Infant</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Neurosurgery - methods</subject><subject>Pediatrics</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgical outcomes</subject><subject>Treatment Outcome</subject><issn>0148-396X</issn><issn>1524-4040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkU1r3DAQhkVoSTYf_yAUQQ49ORmNZFvuLV22aSFfkAZ6M7I9zirY0layS_vvo2XTHnLqaS7P-zAzL2OnAs4FYnlxu3o8hwaEJCm06HUnGtxjC5GjyhQoeMcWIJTOZFX8OGCHMT4DiEKVep8doBBQCl0tWLc0vyg4P0d-Y4beh9FM1rvIfc-nNfHPwVgXJxr5faBIbrLuiVvHl2s7dGvvu0_8YQ5PtjUDX_3eULDkWtoSCvh9cqVIPGbvezNEOnmdR-zxy-r78mt2fXf1bXl5nbVKwZTlOpcS204rISvTI3ZV06DKDRroqTWV1nlTErQNEJV5kTedkoUSRToTEYU8Yh933k3wP2eKUz3a2NIwGEfpwloLpQolYUuevSGf_RxcWq5GCWWJKLFIlNpRbfAxBurrTbCjCX9qAfW2hDqVUL8tIcU-vMrnZqTuX-jv1xNwsQP8vPk_5QtauJFT</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Abla, Adib A</creator><creator>Lekovic, Gregory P</creator><creator>Garrett, Mark</creator><creator>Wilson, David A</creator><creator>Nakaji, Peter</creator><creator>Bristol, Ruth</creator><creator>Spetzler, Robert F</creator><general>Oxford University Press</general><general>Wolters Kluwer Health, Inc</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20101201</creationdate><title>Cavernous Malformations of the Brainstem Presenting in Childhood: Surgical Experience in 40 Patients</title><author>Abla, Adib A ; Lekovic, Gregory P ; Garrett, Mark ; Wilson, David A ; Nakaji, Peter ; Bristol, Ruth ; Spetzler, Robert F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-585332cd84139af22d9bb245a2a0feca9885b7e0cb0ee7565bd43641614822213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Brain Stem - pathology</topic><topic>Brain Stem - surgery</topic><topic>Central Nervous System Vascular Malformations - pathology</topic><topic>Central Nervous System Vascular Malformations - surgery</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Childhood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Infant</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Neurosurgery - methods</topic><topic>Pediatrics</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgical outcomes</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abla, Adib A</creatorcontrib><creatorcontrib>Lekovic, Gregory P</creatorcontrib><creatorcontrib>Garrett, Mark</creatorcontrib><creatorcontrib>Wilson, David A</creatorcontrib><creatorcontrib>Nakaji, Peter</creatorcontrib><creatorcontrib>Bristol, Ruth</creatorcontrib><creatorcontrib>Spetzler, Robert F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abla, Adib A</au><au>Lekovic, Gregory P</au><au>Garrett, Mark</au><au>Wilson, David A</au><au>Nakaji, Peter</au><au>Bristol, Ruth</au><au>Spetzler, Robert F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cavernous Malformations of the Brainstem Presenting in Childhood: Surgical Experience in 40 Patients</atitle><jtitle>Neurosurgery</jtitle><addtitle>Neurosurgery</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>67</volume><issue>6</issue><spage>1589</spage><epage>1599</epage><pages>1589-1599</pages><issn>0148-396X</issn><eissn>1524-4040</eissn><abstract>Abstract
BACKGROUND:
Brainstem cavernous malformations (BSCMs) are believed to compose 9% to 35% of all cerebral cavernous malformations, but these lesions have been reported in children in very limited numbers.
OBJECTIVE:
To review surgical outcomes of pediatric patients with BSCMs treated at 1 institution.
METHODS:
We retrospectively analyzed the course of 40 pediatric patients (19 males, 21 females; age range, 10 months to 18.9 years; mean, 12.3 years) who underwent surgery between 1984 and 2009. Age, sex, presenting symptoms, location of lesion, surgical approach, new postoperative deficits, Glasgow Outcome Scale score, recurrences, and resolution of baseline symptoms were recorded.
RESULTS:
Thirty-nine patients experienced hemorrhage before surgery. Lesion locations included the pons (n = 22), midbrain (n = 4), midbrain and thalamus (n = 4), pontomesencephalic junction (n = 3), medulla (n = 3), pontomedullary junction (n = 3), and cervicomedullary junction (n = 1). Mean lesion size was 2.3 cm. Mean length of hospital stay was 10.7 days. The average clinical follow-up was 31.9 months in 36 patients with follow-up after discharge. At last follow-up, 5 patients had experienced symptoms and/or imaging consistent with rehemorrhage, either from a residual that enlarged or true recurrence (5.25% annual rebleed risk per patient after surgery); 2 required reoperation for further resection of cavernoma. Mean Glasgow Outcome Scale score was 4.2 on admission, 4.05 at discharge, and 4.5 at latest follow-up. Preoperative symptoms and deficits improved in 16 patients (40%). New neurological deficits developed in 19 patients (48%) and resolved in 9, leaving 10 patients (25%) with new permanent deficit.
CONCLUSION:
Compared with adults, pediatric patients with BCSMs tend to have larger lesions and higher rates of recurrence (regrowth of residual lesion). Given the greater life expectancy of children, surgical treatment seems warranted in those with surgically accessible lesions that have bled. Outcomes were similar to those in our adult series of patients with BSCMs.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>21107189</pmid><doi>10.1227/NEU.0b013e3181f8d1b2</doi><tpages>11</tpages></addata></record> |
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subjects | Adolescent Brain Stem - pathology Brain Stem - surgery Central Nervous System Vascular Malformations - pathology Central Nervous System Vascular Malformations - surgery Child Child, Preschool Childhood Female Follow-Up Studies Humans Infant Magnetic Resonance Imaging Male Neurosurgery - methods Pediatrics Retrospective Studies Surgery Surgical outcomes Treatment Outcome |
title | Cavernous Malformations of the Brainstem Presenting in Childhood: Surgical Experience in 40 Patients |
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