Surgical Management of Chiari Malformation Type I and Instability of the Craniocervical Junction Based on Its Pathogenesis and Classification
We investigated the mechanism underlying Chiari malformation type I (CM-I) and classified it according to the morphometric analyses of posterior cranial fossa (PCF) and craniocervical junction (CCJ). Three independent subtypes of CM-I were confirmed (CM-I types A, B, and C) for 484 cases and 150 nor...
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Veröffentlicht in: | Neurologia Medico-Chirurgica 2022/09/15, Vol.62(9), pp.400-415 |
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description | We investigated the mechanism underlying Chiari malformation type I (CM-I) and classified it according to the morphometric analyses of posterior cranial fossa (PCF) and craniocervical junction (CCJ). Three independent subtypes of CM-I were confirmed (CM-I types A, B, and C) for 484 cases and 150 normal volunteers by multiple analyses. CM-I type A had normal volume of PCF (VPCF) and occipital bone size. Type B had normal VPCF and small volume of the area surrounding the foramen magnum (VAFM) and occipital bone size. Type C had small VPCF, VAFM, and occipital bone size. Morphometric analyses during craniocervical traction test demonstrated instability of CCJ. Foramen magnum decompression (FMD) was performed in 302 cases. Expansive suboccipital cranioplasty (ESCP) was performed in 102 cases. Craniocervical posterolateral fixation (CCF) was performed for CCJ instability in 70 cases. Both ESCP and FMD showed a high improvement rate of neurological symptoms and signs (84.4%) and a high recovery rate of the Japanese Orthopaedic Association (JOA) score (58.5%). CCF also showed a high recovery rate of the JOA score (69.7%), with successful joint stabilization (84.3%). CM-I type A was associated with other mechanisms that caused ptosis of the brainstem and cerebellum (CCJ instability and traction and pressure dissociation between the intracranial cavity and spinal canal cavity), whereas CM-I types B and C demonstrated underdevelopment of the occipital bone. For CM-I types B and C, PCF decompression should be performed, whereas for small VPCF, ESCP should be performed. CCF for CCJ instability (including CM-I type A) was safe and effective. |
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Three independent subtypes of CM-I were confirmed (CM-I types A, B, and C) for 484 cases and 150 normal volunteers by multiple analyses. CM-I type A had normal volume of PCF (VPCF) and occipital bone size. Type B had normal VPCF and small volume of the area surrounding the foramen magnum (VAFM) and occipital bone size. Type C had small VPCF, VAFM, and occipital bone size. Morphometric analyses during craniocervical traction test demonstrated instability of CCJ. Foramen magnum decompression (FMD) was performed in 302 cases. Expansive suboccipital cranioplasty (ESCP) was performed in 102 cases. Craniocervical posterolateral fixation (CCF) was performed for CCJ instability in 70 cases. Both ESCP and FMD showed a high improvement rate of neurological symptoms and signs (84.4%) and a high recovery rate of the Japanese Orthopaedic Association (JOA) score (58.5%). CCF also showed a high recovery rate of the JOA score (69.7%), with successful joint stabilization (84.3%). CM-I type A was associated with other mechanisms that caused ptosis of the brainstem and cerebellum (CCJ instability and traction and pressure dissociation between the intracranial cavity and spinal canal cavity), whereas CM-I types B and C demonstrated underdevelopment of the occipital bone. For CM-I types B and C, PCF decompression should be performed, whereas for small VPCF, ESCP should be performed. CCF for CCJ instability (including CM-I type A) was safe and effective.</description><identifier>ISSN: 0470-8105</identifier><identifier>EISSN: 1349-8029</identifier><identifier>DOI: 10.2176/jns-nmc.2022-0078</identifier><identifier>PMID: 36031349</identifier><language>eng</language><publisher>Tokyo: The Japan Neurosurgical Society</publisher><subject>Brain ; Brain stem ; Cerebellum ; Chiari malformation ; Congenital defects ; craniocervical junction ; Decompression ; Instability ; Neural tube defects ; Occipital bone ; pathogenesis ; Skull ; Special Topic ; surgical intervention</subject><ispartof>Neurologia medico-chirurgica, 2022/09/15, Vol.62(9), pp.400-415</ispartof><rights>2022 The Japan Neurosurgical Society</rights><rights>2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c741t-57db16336507a350d5d82735db094820b1b9a1da23f98595fc667f5013912e43</citedby><cites>FETCH-LOGICAL-c741t-57db16336507a350d5d82735db094820b1b9a1da23f98595fc667f5013912e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534572/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534572/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1877,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>NISHIKAWA, Misao</creatorcontrib><creatorcontrib>BOLOGNESE, Paolo A.</creatorcontrib><creatorcontrib>YAMAGATA, Toru</creatorcontrib><creatorcontrib>NAITO, Kentarou</creatorcontrib><creatorcontrib>SAKAMOTO, Hiroaki</creatorcontrib><creatorcontrib>HARA, Mistuhiro</creatorcontrib><creatorcontrib>OHATA, Kenji</creatorcontrib><creatorcontrib>GOTO, Takeo</creatorcontrib><creatorcontrib>Department of Pediatric Neurosurgery</creatorcontrib><creatorcontrib>Chiari Ehlas Danlos Syndrome Center</creatorcontrib><creatorcontrib>Osaka Metropolitan University Graduate School of Medicine</creatorcontrib><creatorcontrib>Department of Neurosurgery</creatorcontrib><creatorcontrib>Moriguchi-Ikuno Memorial Hospital</creatorcontrib><creatorcontrib>Mount Sinai South Nassau</creatorcontrib><creatorcontrib>Osaka City General Hospital</creatorcontrib><creatorcontrib>Naniwa-Ikuno Hospital</creatorcontrib><title>Surgical Management of Chiari Malformation Type I and Instability of the Craniocervical Junction Based on Its Pathogenesis and Classification</title><title>Neurologia Medico-Chirurgica</title><addtitle>Neurol. Med. Chir.(Tokyo)</addtitle><description>We investigated the mechanism underlying Chiari malformation type I (CM-I) and classified it according to the morphometric analyses of posterior cranial fossa (PCF) and craniocervical junction (CCJ). Three independent subtypes of CM-I were confirmed (CM-I types A, B, and C) for 484 cases and 150 normal volunteers by multiple analyses. CM-I type A had normal volume of PCF (VPCF) and occipital bone size. Type B had normal VPCF and small volume of the area surrounding the foramen magnum (VAFM) and occipital bone size. Type C had small VPCF, VAFM, and occipital bone size. Morphometric analyses during craniocervical traction test demonstrated instability of CCJ. Foramen magnum decompression (FMD) was performed in 302 cases. Expansive suboccipital cranioplasty (ESCP) was performed in 102 cases. Craniocervical posterolateral fixation (CCF) was performed for CCJ instability in 70 cases. Both ESCP and FMD showed a high improvement rate of neurological symptoms and signs (84.4%) and a high recovery rate of the Japanese Orthopaedic Association (JOA) score (58.5%). CCF also showed a high recovery rate of the JOA score (69.7%), with successful joint stabilization (84.3%). CM-I type A was associated with other mechanisms that caused ptosis of the brainstem and cerebellum (CCJ instability and traction and pressure dissociation between the intracranial cavity and spinal canal cavity), whereas CM-I types B and C demonstrated underdevelopment of the occipital bone. For CM-I types B and C, PCF decompression should be performed, whereas for small VPCF, ESCP should be performed. CCF for CCJ instability (including CM-I type A) was safe and effective.</description><subject>Brain</subject><subject>Brain stem</subject><subject>Cerebellum</subject><subject>Chiari malformation</subject><subject>Congenital defects</subject><subject>craniocervical junction</subject><subject>Decompression</subject><subject>Instability</subject><subject>Neural tube defects</subject><subject>Occipital bone</subject><subject>pathogenesis</subject><subject>Skull</subject><subject>Special Topic</subject><subject>surgical intervention</subject><issn>0470-8105</issn><issn>1349-8029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkt9u0zAUxiMEYtXYA3AXieuM4__xDRJEbBQNgUTvLcdxUlepXexkUh-Cd8Zpt6Ld2Jb9nd9nH39F8R7BLUaCf9z5VPm9ucWAcQUg6lfFChEqqxqwfF2sgAqoagTsqrhJybUAmNaU1OJtcUU4kEW7Kv7-nuPgjB7LH9rrwe6tn8rQl83W6ejy5tiHuNeTC77cHA-2XJfad-Xap0m3bnTTcVFPW1s2UXsXjI2PJ9z32ZtT1RedbFfmxXpK5S89bcNgvU0unUDNqPPl-lyyiN8Vb3o9JnvzNF8Xm7uvm-Zb9fDzft18fqiMoGiqmOhaxAnhDIQmDDrW1VgQ1rUgaY2hRa3UqNOY9LJmkvWGc9EzQEQibCm5LtZnbBf0Th2i2-t4VEE7ddoIcVA6Ts6MVmnTSwnGtD03VAKSvMut60TbZzNNbWZ9OrMOc7u3ncn9i3p8AX154t1WDeFRSUYoEzgDPjwBYvgz2zSpXZijz89XWGBAwDmqswqdVSaGlKLtLw4I1JIHlfOgch7Ukge15CHX3J9rsvvyJ8GPztv_eNMhb-don0s4BpmnvKQAeUCMAheslpnUnEm7_O2DvXg_d2nx5VjJZbj4X07NVkdlPfkHYH7Ymg</recordid><startdate>20220915</startdate><enddate>20220915</enddate><creator>NISHIKAWA, Misao</creator><creator>BOLOGNESE, Paolo A.</creator><creator>YAMAGATA, Toru</creator><creator>NAITO, Kentarou</creator><creator>SAKAMOTO, Hiroaki</creator><creator>HARA, Mistuhiro</creator><creator>OHATA, Kenji</creator><creator>GOTO, Takeo</creator><general>The Japan Neurosurgical Society</general><general>THE JAPAN NEUROSURGICAL SOCIETY</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220915</creationdate><title>Surgical Management of Chiari Malformation Type I and Instability of the Craniocervical Junction Based on Its Pathogenesis and Classification</title><author>NISHIKAWA, Misao ; BOLOGNESE, Paolo A. ; YAMAGATA, Toru ; NAITO, Kentarou ; SAKAMOTO, Hiroaki ; HARA, Mistuhiro ; OHATA, Kenji ; GOTO, Takeo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c741t-57db16336507a350d5d82735db094820b1b9a1da23f98595fc667f5013912e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Brain</topic><topic>Brain stem</topic><topic>Cerebellum</topic><topic>Chiari malformation</topic><topic>Congenital defects</topic><topic>craniocervical junction</topic><topic>Decompression</topic><topic>Instability</topic><topic>Neural tube defects</topic><topic>Occipital bone</topic><topic>pathogenesis</topic><topic>Skull</topic><topic>Special Topic</topic><topic>surgical intervention</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NISHIKAWA, Misao</creatorcontrib><creatorcontrib>BOLOGNESE, Paolo A.</creatorcontrib><creatorcontrib>YAMAGATA, Toru</creatorcontrib><creatorcontrib>NAITO, Kentarou</creatorcontrib><creatorcontrib>SAKAMOTO, Hiroaki</creatorcontrib><creatorcontrib>HARA, Mistuhiro</creatorcontrib><creatorcontrib>OHATA, Kenji</creatorcontrib><creatorcontrib>GOTO, Takeo</creatorcontrib><creatorcontrib>Department of Pediatric Neurosurgery</creatorcontrib><creatorcontrib>Chiari Ehlas Danlos Syndrome Center</creatorcontrib><creatorcontrib>Osaka Metropolitan University Graduate School of Medicine</creatorcontrib><creatorcontrib>Department of Neurosurgery</creatorcontrib><creatorcontrib>Moriguchi-Ikuno Memorial Hospital</creatorcontrib><creatorcontrib>Mount Sinai South Nassau</creatorcontrib><creatorcontrib>Osaka City General Hospital</creatorcontrib><creatorcontrib>Naniwa-Ikuno Hospital</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Neurologia Medico-Chirurgica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NISHIKAWA, Misao</au><au>BOLOGNESE, Paolo A.</au><au>YAMAGATA, Toru</au><au>NAITO, Kentarou</au><au>SAKAMOTO, Hiroaki</au><au>HARA, Mistuhiro</au><au>OHATA, Kenji</au><au>GOTO, Takeo</au><aucorp>Department of Pediatric Neurosurgery</aucorp><aucorp>Chiari Ehlas Danlos Syndrome Center</aucorp><aucorp>Osaka Metropolitan University Graduate School of Medicine</aucorp><aucorp>Department of Neurosurgery</aucorp><aucorp>Moriguchi-Ikuno Memorial Hospital</aucorp><aucorp>Mount Sinai South Nassau</aucorp><aucorp>Osaka City General Hospital</aucorp><aucorp>Naniwa-Ikuno Hospital</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surgical Management of Chiari Malformation Type I and Instability of the Craniocervical Junction Based on Its Pathogenesis and Classification</atitle><jtitle>Neurologia Medico-Chirurgica</jtitle><addtitle>Neurol. Med. Chir.(Tokyo)</addtitle><date>2022-09-15</date><risdate>2022</risdate><volume>62</volume><issue>9</issue><spage>400</spage><epage>415</epage><pages>400-415</pages><artnum>2022-0078</artnum><issn>0470-8105</issn><eissn>1349-8029</eissn><abstract>We investigated the mechanism underlying Chiari malformation type I (CM-I) and classified it according to the morphometric analyses of posterior cranial fossa (PCF) and craniocervical junction (CCJ). Three independent subtypes of CM-I were confirmed (CM-I types A, B, and C) for 484 cases and 150 normal volunteers by multiple analyses. CM-I type A had normal volume of PCF (VPCF) and occipital bone size. Type B had normal VPCF and small volume of the area surrounding the foramen magnum (VAFM) and occipital bone size. Type C had small VPCF, VAFM, and occipital bone size. Morphometric analyses during craniocervical traction test demonstrated instability of CCJ. Foramen magnum decompression (FMD) was performed in 302 cases. Expansive suboccipital cranioplasty (ESCP) was performed in 102 cases. Craniocervical posterolateral fixation (CCF) was performed for CCJ instability in 70 cases. Both ESCP and FMD showed a high improvement rate of neurological symptoms and signs (84.4%) and a high recovery rate of the Japanese Orthopaedic Association (JOA) score (58.5%). CCF also showed a high recovery rate of the JOA score (69.7%), with successful joint stabilization (84.3%). CM-I type A was associated with other mechanisms that caused ptosis of the brainstem and cerebellum (CCJ instability and traction and pressure dissociation between the intracranial cavity and spinal canal cavity), whereas CM-I types B and C demonstrated underdevelopment of the occipital bone. For CM-I types B and C, PCF decompression should be performed, whereas for small VPCF, ESCP should be performed. CCF for CCJ instability (including CM-I type A) was safe and effective.</abstract><cop>Tokyo</cop><pub>The Japan Neurosurgical Society</pub><pmid>36031349</pmid><doi>10.2176/jns-nmc.2022-0078</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Brain Brain stem Cerebellum Chiari malformation Congenital defects craniocervical junction Decompression Instability Neural tube defects Occipital bone pathogenesis Skull Special Topic surgical intervention |
title | Surgical Management of Chiari Malformation Type I and Instability of the Craniocervical Junction Based on Its Pathogenesis and Classification |
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