Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy
Abstract OBJECTIVE Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization...
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Veröffentlicht in: | Neurosurgery 2008-12, Vol.63 (6), p.1130-1138 |
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description | Abstract
OBJECTIVE
Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures.
METHODS
Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual.
RESULTS
Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively).
CONCLUSION
MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE. |
doi_str_mv | 10.1227/01.NEU.0000334429.15867.3B |
format | Article |
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OBJECTIVE
Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures.
METHODS
Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual.
RESULTS
Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively).
CONCLUSION
MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</description><identifier>ISSN: 0148-396X</identifier><identifier>EISSN: 1524-4040</identifier><identifier>DOI: 10.1227/01.NEU.0000334429.15867.3B</identifier><identifier>PMID: 19057325</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adolescent ; Adult ; Epilepsy ; Epilepsy, Temporal Lobe - diagnostic imaging ; Epilepsy, Temporal Lobe - pathology ; Female ; Fluorodeoxyglucose F18 ; Humans ; Magnetic Resonance Imaging ; Male ; Metabolism ; Middle Aged ; NMR ; Nuclear magnetic resonance ; Positron-Emission Tomography - methods ; Radiopharmaceuticals ; Reproducibility of Results ; Sensitivity and Specificity ; Tomography ; Young Adult</subject><ispartof>Neurosurgery, 2008-12, Vol.63 (6), p.1130-1138</ispartof><rights>2008 by the Congress of Neurological Surgeons</rights><rights>Copyright © Congress of Neurological Surgeons</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</citedby><cites>FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19057325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boling, Warren W.</creatorcontrib><creatorcontrib>Lancaster, Melissa</creatorcontrib><creatorcontrib>Kraszpulski, Michal</creatorcontrib><creatorcontrib>Palade, Adriana</creatorcontrib><creatorcontrib>Marano, Gary</creatorcontrib><creatorcontrib>Puce, Aina</creatorcontrib><title>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</title><title>Neurosurgery</title><addtitle>Neurosurgery</addtitle><description>Abstract
OBJECTIVE
Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures.
METHODS
Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual.
RESULTS
Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively).
CONCLUSION
MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Epilepsy</subject><subject>Epilepsy, Temporal Lobe - diagnostic imaging</subject><subject>Epilepsy, Temporal Lobe - pathology</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Metabolism</subject><subject>Middle Aged</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Positron-Emission Tomography - methods</subject><subject>Radiopharmaceuticals</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Tomography</subject><subject>Young Adult</subject><issn>0148-396X</issn><issn>1524-4040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqVkc1u1DAQxy0EokvhFZAFErcEO3b8wY22W1pp-ThsJW6W40xSV0kc7I3UvfEOvCFPgumuVIkbc_Ecfv-ZsX4IvaGkpFUl3xNaflnflCQXY5xXuqS1ErJkZ0_QitYVLzjh5ClaEcpVwbT4foJepHRHCBVcqufohGpSS1bVKzReDkuIoYVwv--HxYUEv3_--haS38Uw4fXoU_K52YYx9NHOt97h69H2fupxFyLe3QK-8LafciLh0OHPkLwd8BbGOcTcbEIDeD37Aea0f4medXZI8Or4nqKby_X2_KrYfP10ff5xUzhGxK6gVnSgaKskt1RorRjpWKsr4VreAXNOSRCON7VSRGgQSjbUVU0n2lYBUTU7Re8Oc-cYfiyQdib_w8Ew2AnCkozQSkpa8Qy-_Qe8C0uc8m2GalULxRSRmfpwoFwMKUXozBz9aOPeUGL-KjGEmqzEPCoxD0oMO8vh18cVSzNC-xg9OshAfQDCMv_P4D9-_ZmA</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Boling, Warren W.</creator><creator>Lancaster, Melissa</creator><creator>Kraszpulski, Michal</creator><creator>Palade, Adriana</creator><creator>Marano, Gary</creator><creator>Puce, Aina</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>20081201</creationdate><title>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</title><author>Boling, Warren W. ; Lancaster, Melissa ; Kraszpulski, Michal ; Palade, Adriana ; Marano, Gary ; Puce, Aina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-1a6fe81d874a1699830f3d926cd4fe3cc87e6c4b588069e687b1c2bf6dd8e0853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Epilepsy</topic><topic>Epilepsy, Temporal Lobe - diagnostic imaging</topic><topic>Epilepsy, Temporal Lobe - pathology</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Metabolism</topic><topic>Middle Aged</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Positron-Emission Tomography - methods</topic><topic>Radiopharmaceuticals</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Tomography</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boling, Warren W.</creatorcontrib><creatorcontrib>Lancaster, Melissa</creatorcontrib><creatorcontrib>Kraszpulski, Michal</creatorcontrib><creatorcontrib>Palade, Adriana</creatorcontrib><creatorcontrib>Marano, Gary</creatorcontrib><creatorcontrib>Puce, Aina</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>Boling, Warren W.</au><au>Lancaster, Melissa</au><au>Kraszpulski, Michal</au><au>Palade, Adriana</au><au>Marano, Gary</au><au>Puce, Aina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy</atitle><jtitle>Neurosurgery</jtitle><addtitle>Neurosurgery</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>63</volume><issue>6</issue><spage>1130</spage><epage>1138</epage><pages>1130-1138</pages><issn>0148-396X</issn><eissn>1524-4040</eissn><abstract>Abstract
OBJECTIVE
Fluorodeoxyglucose (FDG)-positron emission tomographic (PET) imaging plays an important role in the evaluation of intractable epilepsy. The metabolic defect has proven utility in the lateralization of temporal lobe epilepsy. However, the role of FDG–PET imaging in the localization of a seizure focus within the temporal lobe is uncertain. We evaluated FDG–PET imaging for the capability to localize a temporal seizure focus within the mesial structures.
METHODS
Twenty-eight patients who underwent selective amygdalohippocampectomy for intractable temporal lobe epilepsy were studied. Patients were divided into 2 groups: those who were free of seizures (FS) and those with persisting seizures postoperatively. FS patients were defined by having mesial temporal lobe epilepsy (MTLE). Preoperative FDG–PET activity was evaluated in temporal lobe structures and contrasted with magnetic resonance imaging (MRI) for usefulness in identifying MTLE in an individual.
RESULTS
Pathology of the hippocampus revealed mesial temporal sclerosis in all but 1 patient. Qualitative visual inspection of the MRI scan was not reliable in the identification of MTLE (P = 0.15). MRI volumetry found smaller mesial temporal structures (P = 0.04) in FS patients. Mesial temporal metabolic activity was reduced in the FS group (hippocampus, P = 0.001). However, a combination of imaging modalities was found to be the best predictor of MTLE. PET imaging plus MRI qualitative inspection identified all patients with and without MTLE correctly and was superior to MRI alone (P = 0.01 and P = 0.02, respectively).
CONCLUSION
MRI volumetry and PET imaging were comparable (P = 0.73) and able to identify MTLE in most patients, but a combination of PET imaging and MRI visual inspection was superior in the recognition of MTLE.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>19057325</pmid><doi>10.1227/01.NEU.0000334429.15867.3B</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Epilepsy Epilepsy, Temporal Lobe - diagnostic imaging Epilepsy, Temporal Lobe - pathology Female Fluorodeoxyglucose F18 Humans Magnetic Resonance Imaging Male Metabolism Middle Aged NMR Nuclear magnetic resonance Positron-Emission Tomography - methods Radiopharmaceuticals Reproducibility of Results Sensitivity and Specificity Tomography Young Adult |
title | Fluorodeoxyglucose–Positron Emission Tomographic Imaging for the Diagnosis of Mesial Temporal Lobe Epilepsy |
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