Canine intracranial neoplasia: clinical risk factors for development of epileptic seizures

Objectives: To identify clinical risk factors for seizures in dogs with intracranial neoplasia. Methods: A cross‐sectional retrospective study of 68 dogs with histopathologically confirmed primary or secondary intracranial neoplasia, complete clinical history and magnetic resonance imaging of the br...

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Veröffentlicht in:Journal of small animal practice 2011-12, Vol.52 (12), p.632-637
Hauptverfasser: Schwartz, M., Lamb, C. R., Brodbelt, D. C., Volk, H. A.
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container_issue 12
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container_title Journal of small animal practice
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creator Schwartz, M.
Lamb, C. R.
Brodbelt, D. C.
Volk, H. A.
description Objectives: To identify clinical risk factors for seizures in dogs with intracranial neoplasia. Methods: A cross‐sectional retrospective study of 68 dogs with histopathologically confirmed primary or secondary intracranial neoplasia, complete clinical history and magnetic resonance imaging of the brain was conducted. Signalment and clinical history were retrieved from clinical records and magnetic resonance images of the brain were re‐evaluated. Prevalence of findings was compared between dogs with and without seizures. Results: Forty‐two dogs had tumour‐related seizures, the remaining 26 were seizure‐free. Tumour types included meningioma (23 dogs with and 5 without seizures), glioma (9 dogs with and 6 without seizures), choroid plexus tumour (2 dogs without seizures), neuroblastoma (1 dog with seizures) and metastatic/invasive tumours including lymphoma (9 dogs with and 13 without seizures). On the basis of multi‐variable logistic regression analysis, risk factors for seizures associated with intracranial neoplasia were magnetic resonance imaging findings consistent with the presence of neoplastic tissue in frontal lobe [odds ratio (OR) 9·61; 95% confidence interval (CI) 2·59 to 35·61], marked gadolinium enhancement (OR 10·41; 95% CI 2·07 to 52·30) and magnetic resonance imaging findings of subfalcine and/or subtentorial herniation (OR 3·88; 95% CI 1·10 to 13·71). Clinical Significance: Dogs with primary or secondary intracranial neoplasia are at risk of seizures, particularly those with tumours that affect the frontal lobe, enhance markedly with gadolinium, or cause subfalcine and/or subtentorial herniation.
doi_str_mv 10.1111/j.1748-5827.2011.01131.x
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R. ; Brodbelt, D. C. ; Volk, H. A.</creator><creatorcontrib>Schwartz, M. ; Lamb, C. R. ; Brodbelt, D. C. ; Volk, H. A.</creatorcontrib><description>Objectives: To identify clinical risk factors for seizures in dogs with intracranial neoplasia. Methods: A cross‐sectional retrospective study of 68 dogs with histopathologically confirmed primary or secondary intracranial neoplasia, complete clinical history and magnetic resonance imaging of the brain was conducted. Signalment and clinical history were retrieved from clinical records and magnetic resonance images of the brain were re‐evaluated. Prevalence of findings was compared between dogs with and without seizures. Results: Forty‐two dogs had tumour‐related seizures, the remaining 26 were seizure‐free. Tumour types included meningioma (23 dogs with and 5 without seizures), glioma (9 dogs with and 6 without seizures), choroid plexus tumour (2 dogs without seizures), neuroblastoma (1 dog with seizures) and metastatic/invasive tumours including lymphoma (9 dogs with and 13 without seizures). On the basis of multi‐variable logistic regression analysis, risk factors for seizures associated with intracranial neoplasia were magnetic resonance imaging findings consistent with the presence of neoplastic tissue in frontal lobe [odds ratio (OR) 9·61; 95% confidence interval (CI) 2·59 to 35·61], marked gadolinium enhancement (OR 10·41; 95% CI 2·07 to 52·30) and magnetic resonance imaging findings of subfalcine and/or subtentorial herniation (OR 3·88; 95% CI 1·10 to 13·71). Clinical Significance: Dogs with primary or secondary intracranial neoplasia are at risk of seizures, particularly those with tumours that affect the frontal lobe, enhance markedly with gadolinium, or cause subfalcine and/or subtentorial herniation.</description><identifier>ISSN: 0022-4510</identifier><identifier>EISSN: 1748-5827</identifier><identifier>DOI: 10.1111/j.1748-5827.2011.01131.x</identifier><identifier>PMID: 21954970</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Brain ; Brain Neoplasms - complications ; Brain Neoplasms - epidemiology ; Brain Neoplasms - pathology ; Brain Neoplasms - veterinary ; Brain tumors ; Causality ; Choroid plexus ; Comorbidity ; Cross-Sectional Studies ; Dog Diseases - epidemiology ; Dog Diseases - etiology ; Dog Diseases - pathology ; Dogs ; Epilepsy ; Epilepsy - epidemiology ; Epilepsy - etiology ; Epilepsy - pathology ; Epilepsy - veterinary ; Female ; Frontal lobe ; Gadolinium ; Glioma ; Invasiveness ; Lymphoma ; Magnetic resonance imaging ; Magnetic Resonance Imaging - veterinary ; Male ; meningioma ; Metastases ; Neoplasia ; Neuroblastoma ; Neuroimaging ; Neurologic Examination - veterinary ; Regression analysis ; Retrospective Studies ; Risk Factors ; Seizures</subject><ispartof>Journal of small animal practice, 2011-12, Vol.52 (12), p.632-637</ispartof><rights>2011 British Small Animal Veterinary Association</rights><rights>2011 British Small Animal Veterinary Association.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5061-43e6a42c3758108eb1195c682e982ad5df7f28f309550193d41b66da2a34d6073</citedby><cites>FETCH-LOGICAL-c5061-43e6a42c3758108eb1195c682e982ad5df7f28f309550193d41b66da2a34d6073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1748-5827.2011.01131.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1748-5827.2011.01131.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21954970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwartz, M.</creatorcontrib><creatorcontrib>Lamb, C. R.</creatorcontrib><creatorcontrib>Brodbelt, D. C.</creatorcontrib><creatorcontrib>Volk, H. A.</creatorcontrib><title>Canine intracranial neoplasia: clinical risk factors for development of epileptic seizures</title><title>Journal of small animal practice</title><addtitle>J Small Anim Pract</addtitle><description>Objectives: To identify clinical risk factors for seizures in dogs with intracranial neoplasia. Methods: A cross‐sectional retrospective study of 68 dogs with histopathologically confirmed primary or secondary intracranial neoplasia, complete clinical history and magnetic resonance imaging of the brain was conducted. Signalment and clinical history were retrieved from clinical records and magnetic resonance images of the brain were re‐evaluated. Prevalence of findings was compared between dogs with and without seizures. Results: Forty‐two dogs had tumour‐related seizures, the remaining 26 were seizure‐free. Tumour types included meningioma (23 dogs with and 5 without seizures), glioma (9 dogs with and 6 without seizures), choroid plexus tumour (2 dogs without seizures), neuroblastoma (1 dog with seizures) and metastatic/invasive tumours including lymphoma (9 dogs with and 13 without seizures). On the basis of multi‐variable logistic regression analysis, risk factors for seizures associated with intracranial neoplasia were magnetic resonance imaging findings consistent with the presence of neoplastic tissue in frontal lobe [odds ratio (OR) 9·61; 95% confidence interval (CI) 2·59 to 35·61], marked gadolinium enhancement (OR 10·41; 95% CI 2·07 to 52·30) and magnetic resonance imaging findings of subfalcine and/or subtentorial herniation (OR 3·88; 95% CI 1·10 to 13·71). Clinical Significance: Dogs with primary or secondary intracranial neoplasia are at risk of seizures, particularly those with tumours that affect the frontal lobe, enhance markedly with gadolinium, or cause subfalcine and/or subtentorial herniation.</description><subject>Animals</subject><subject>Brain</subject><subject>Brain Neoplasms - complications</subject><subject>Brain Neoplasms - epidemiology</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain Neoplasms - veterinary</subject><subject>Brain tumors</subject><subject>Causality</subject><subject>Choroid plexus</subject><subject>Comorbidity</subject><subject>Cross-Sectional Studies</subject><subject>Dog Diseases - epidemiology</subject><subject>Dog Diseases - etiology</subject><subject>Dog Diseases - pathology</subject><subject>Dogs</subject><subject>Epilepsy</subject><subject>Epilepsy - epidemiology</subject><subject>Epilepsy - etiology</subject><subject>Epilepsy - pathology</subject><subject>Epilepsy - veterinary</subject><subject>Female</subject><subject>Frontal lobe</subject><subject>Gadolinium</subject><subject>Glioma</subject><subject>Invasiveness</subject><subject>Lymphoma</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - veterinary</subject><subject>Male</subject><subject>meningioma</subject><subject>Metastases</subject><subject>Neoplasia</subject><subject>Neuroblastoma</subject><subject>Neuroimaging</subject><subject>Neurologic Examination - veterinary</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Seizures</subject><issn>0022-4510</issn><issn>1748-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV1v0zAUhi3ExLrCX0C-g5sEf9vhAmmqWGGaxtBASNxYrnMiuUuTzE5Zt18_h45eolm27GM_57X9HoQwJSXN7cO6pFqYQhqmS0YoLfPgtNy9QLPDwUs0I4SxQkhKjtFJSuscKqHJK3TMaCVFpckM_V64LnSAQzdG52MOXIs76IfWpeA-Yt-GLvi8F0O6wY3zYx8TbvqIa_gDbT9soBtx32AYQgvDGDxOEB62EdJrdNS4NsGbp3mOfp59_rH4Ulx8W35dnF4UXhJFC8FBOcE819JQYmBF8-O8Mgwqw1wt60Y3zDScVFISWvFa0JVStWOOi1oRzefo3V53iP3tFtJoNyF5aFuX_7FNtiJGC8pzn6P3_yUpqbhQggmRUbNHfexTitDYIYaNi_cZslMN7NpOVtvJajvVwP6tgd3l1LdPt2xXG6gPif9Mz8CnPXCXLbt_trA9vz69mpZZoNgLhDTC7iDg4o1VOvtof10u7dWSXJ9JJu13_giq8KPG</recordid><startdate>201112</startdate><enddate>201112</enddate><creator>Schwartz, M.</creator><creator>Lamb, C. 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A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5061-43e6a42c3758108eb1195c682e982ad5df7f28f309550193d41b66da2a34d6073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Brain</topic><topic>Brain Neoplasms - complications</topic><topic>Brain Neoplasms - epidemiology</topic><topic>Brain Neoplasms - pathology</topic><topic>Brain Neoplasms - veterinary</topic><topic>Brain tumors</topic><topic>Causality</topic><topic>Choroid plexus</topic><topic>Comorbidity</topic><topic>Cross-Sectional Studies</topic><topic>Dog Diseases - epidemiology</topic><topic>Dog Diseases - etiology</topic><topic>Dog Diseases - pathology</topic><topic>Dogs</topic><topic>Epilepsy</topic><topic>Epilepsy - epidemiology</topic><topic>Epilepsy - etiology</topic><topic>Epilepsy - pathology</topic><topic>Epilepsy - veterinary</topic><topic>Female</topic><topic>Frontal lobe</topic><topic>Gadolinium</topic><topic>Glioma</topic><topic>Invasiveness</topic><topic>Lymphoma</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - veterinary</topic><topic>Male</topic><topic>meningioma</topic><topic>Metastases</topic><topic>Neoplasia</topic><topic>Neuroblastoma</topic><topic>Neuroimaging</topic><topic>Neurologic Examination - veterinary</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Seizures</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwartz, M.</creatorcontrib><creatorcontrib>Lamb, C. R.</creatorcontrib><creatorcontrib>Brodbelt, D. C.</creatorcontrib><creatorcontrib>Volk, H. A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of small animal practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwartz, M.</au><au>Lamb, C. R.</au><au>Brodbelt, D. C.</au><au>Volk, H. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Canine intracranial neoplasia: clinical risk factors for development of epileptic seizures</atitle><jtitle>Journal of small animal practice</jtitle><addtitle>J Small Anim Pract</addtitle><date>2011-12</date><risdate>2011</risdate><volume>52</volume><issue>12</issue><spage>632</spage><epage>637</epage><pages>632-637</pages><issn>0022-4510</issn><eissn>1748-5827</eissn><abstract>Objectives: To identify clinical risk factors for seizures in dogs with intracranial neoplasia. Methods: A cross‐sectional retrospective study of 68 dogs with histopathologically confirmed primary or secondary intracranial neoplasia, complete clinical history and magnetic resonance imaging of the brain was conducted. Signalment and clinical history were retrieved from clinical records and magnetic resonance images of the brain were re‐evaluated. Prevalence of findings was compared between dogs with and without seizures. Results: Forty‐two dogs had tumour‐related seizures, the remaining 26 were seizure‐free. Tumour types included meningioma (23 dogs with and 5 without seizures), glioma (9 dogs with and 6 without seizures), choroid plexus tumour (2 dogs without seizures), neuroblastoma (1 dog with seizures) and metastatic/invasive tumours including lymphoma (9 dogs with and 13 without seizures). On the basis of multi‐variable logistic regression analysis, risk factors for seizures associated with intracranial neoplasia were magnetic resonance imaging findings consistent with the presence of neoplastic tissue in frontal lobe [odds ratio (OR) 9·61; 95% confidence interval (CI) 2·59 to 35·61], marked gadolinium enhancement (OR 10·41; 95% CI 2·07 to 52·30) and magnetic resonance imaging findings of subfalcine and/or subtentorial herniation (OR 3·88; 95% CI 1·10 to 13·71). Clinical Significance: Dogs with primary or secondary intracranial neoplasia are at risk of seizures, particularly those with tumours that affect the frontal lobe, enhance markedly with gadolinium, or cause subfalcine and/or subtentorial herniation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21954970</pmid><doi>10.1111/j.1748-5827.2011.01131.x</doi><tpages>6</tpages></addata></record>
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subjects Animals
Brain
Brain Neoplasms - complications
Brain Neoplasms - epidemiology
Brain Neoplasms - pathology
Brain Neoplasms - veterinary
Brain tumors
Causality
Choroid plexus
Comorbidity
Cross-Sectional Studies
Dog Diseases - epidemiology
Dog Diseases - etiology
Dog Diseases - pathology
Dogs
Epilepsy
Epilepsy - epidemiology
Epilepsy - etiology
Epilepsy - pathology
Epilepsy - veterinary
Female
Frontal lobe
Gadolinium
Glioma
Invasiveness
Lymphoma
Magnetic resonance imaging
Magnetic Resonance Imaging - veterinary
Male
meningioma
Metastases
Neoplasia
Neuroblastoma
Neuroimaging
Neurologic Examination - veterinary
Regression analysis
Retrospective Studies
Risk Factors
Seizures
title Canine intracranial neoplasia: clinical risk factors for development of epileptic seizures
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