MRI of the fornix and mamillary body in temporal lobe epilepsy
We performed MRI on 27 patients with clinically proven temporal lobe epilepsy (TLE), all with prior EEG lateralisation, and 10 volunteers, studied to evaluate disparity in size arising from biological variation (group 1). Three-dimensional spoiled GRASS (3DSPGR) sequences provided 2-mm contiguous se...
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Veröffentlicht in: | Neuroradiology 1997-08, Vol.39 (8), p.551-555 |
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description | We performed MRI on 27 patients with clinically proven temporal lobe epilepsy (TLE), all with prior EEG lateralisation, and 10 volunteers, studied to evaluate disparity in size arising from biological variation (group 1). Three-dimensional spoiled GRASS (3DSPGR) sequences provided 2-mm contiguous sections of the limbic system, enabling assessment of the hippocampus (HC), fornix (FN) and mamillary body (MB). Measurements of FN and MB width were made from a workstation. Any percentage difference in size was computed. In 19 cases there was unilateral abnormality in the HC (group 2); in 18 and 19 cases respectively there was a smaller FN and MB on the same side as the abnormal HC. This percentage difference in size was significantly greater than that in group 1 in the FN and MB in 17 and 17 cases respectively. Comparison of percentage difference computations for FN and MB between groups 1 and 2 showed high statistical significance (P < 0.0002). In 5 patients with clinical TLE the HC was normal on MRI (group 3). Unequal FN and MB sizes were found in 4, significant in 2. Comparison of percentage difference computations for FN and MB showed statistical significance (P < 0.0005 and P < 0.0003 respectively). There was no case of discordance between the sides of hippocampal abnormality and the smaller FN or MB or between the sides of smaller FN and MB. The strong concordance between the changes in the HC and those in the FN and MB suggests that this combination will play an important role in the assessment of TLE and limbic system abnormality. |
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E. S ; LAU, T. N ; HUI, F. K. H ; CHUA, G. E ; LEE, W. L ; CHEE, M. W. L ; CHEE, T. S. G ; BOEY, H. K</creator><creatorcontrib>NG, S. E. S ; LAU, T. N ; HUI, F. K. H ; CHUA, G. E ; LEE, W. L ; CHEE, M. W. L ; CHEE, T. S. G ; BOEY, H. K</creatorcontrib><description>We performed MRI on 27 patients with clinically proven temporal lobe epilepsy (TLE), all with prior EEG lateralisation, and 10 volunteers, studied to evaluate disparity in size arising from biological variation (group 1). Three-dimensional spoiled GRASS (3DSPGR) sequences provided 2-mm contiguous sections of the limbic system, enabling assessment of the hippocampus (HC), fornix (FN) and mamillary body (MB). Measurements of FN and MB width were made from a workstation. Any percentage difference in size was computed. In 19 cases there was unilateral abnormality in the HC (group 2); in 18 and 19 cases respectively there was a smaller FN and MB on the same side as the abnormal HC. This percentage difference in size was significantly greater than that in group 1 in the FN and MB in 17 and 17 cases respectively. Comparison of percentage difference computations for FN and MB between groups 1 and 2 showed high statistical significance (P < 0.0002). In 5 patients with clinical TLE the HC was normal on MRI (group 3). Unequal FN and MB sizes were found in 4, significant in 2. Comparison of percentage difference computations for FN and MB showed statistical significance (P < 0.0005 and P < 0.0003 respectively). There was no case of discordance between the sides of hippocampal abnormality and the smaller FN or MB or between the sides of smaller FN and MB. The strong concordance between the changes in the HC and those in the FN and MB suggests that this combination will play an important role in the assessment of TLE and limbic system abnormality.</description><identifier>ISSN: 0028-3940</identifier><identifier>EISSN: 1432-1920</identifier><identifier>DOI: 10.1007/s002340050465</identifier><identifier>PMID: 9272490</identifier><identifier>CODEN: NRDYAB</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Child, Preschool ; Dominance, Cerebral - physiology ; Electroencephalography ; Epilepsy, Temporal Lobe - diagnosis ; Epilepsy, Temporal Lobe - pathology ; Epilepsy, Temporal Lobe - surgery ; Female ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Hippocampus - pathology ; Hippocampus - surgery ; Humans ; Image Processing, Computer-Assisted ; Limbic System - pathology ; Limbic System - surgery ; Male ; Mammillary Bodies - pathology ; Mammillary Bodies - surgery ; Medical sciences ; Middle Aged ; Nervous system (semeiology, syndromes) ; Neuroglia - pathology ; Neurology ; Neurons - pathology ; Psychosurgery ; Sensitivity and Specificity ; Temporal Lobe - pathology ; Temporal Lobe - surgery ; Tropical medicine ; Wallerian Degeneration - physiology</subject><ispartof>Neuroradiology, 1997-08, Vol.39 (8), p.551-555</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-afaff05569c7aab0fc2bfbe31cf6eee893efc82bd612c2096909cae445ba2e3f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2764731$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9272490$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NG, S. E. S</creatorcontrib><creatorcontrib>LAU, T. N</creatorcontrib><creatorcontrib>HUI, F. K. H</creatorcontrib><creatorcontrib>CHUA, G. E</creatorcontrib><creatorcontrib>LEE, W. L</creatorcontrib><creatorcontrib>CHEE, M. W. L</creatorcontrib><creatorcontrib>CHEE, T. S. G</creatorcontrib><creatorcontrib>BOEY, H. K</creatorcontrib><title>MRI of the fornix and mamillary body in temporal lobe epilepsy</title><title>Neuroradiology</title><addtitle>Neuroradiology</addtitle><description>We performed MRI on 27 patients with clinically proven temporal lobe epilepsy (TLE), all with prior EEG lateralisation, and 10 volunteers, studied to evaluate disparity in size arising from biological variation (group 1). Three-dimensional spoiled GRASS (3DSPGR) sequences provided 2-mm contiguous sections of the limbic system, enabling assessment of the hippocampus (HC), fornix (FN) and mamillary body (MB). Measurements of FN and MB width were made from a workstation. Any percentage difference in size was computed. In 19 cases there was unilateral abnormality in the HC (group 2); in 18 and 19 cases respectively there was a smaller FN and MB on the same side as the abnormal HC. This percentage difference in size was significantly greater than that in group 1 in the FN and MB in 17 and 17 cases respectively. Comparison of percentage difference computations for FN and MB between groups 1 and 2 showed high statistical significance (P < 0.0002). In 5 patients with clinical TLE the HC was normal on MRI (group 3). Unequal FN and MB sizes were found in 4, significant in 2. Comparison of percentage difference computations for FN and MB showed statistical significance (P < 0.0005 and P < 0.0003 respectively). There was no case of discordance between the sides of hippocampal abnormality and the smaller FN or MB or between the sides of smaller FN and MB. The strong concordance between the changes in the HC and those in the FN and MB suggests that this combination will play an important role in the assessment of TLE and limbic system abnormality.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Dominance, Cerebral - physiology</subject><subject>Electroencephalography</subject><subject>Epilepsy, Temporal Lobe - diagnosis</subject><subject>Epilepsy, Temporal Lobe - pathology</subject><subject>Epilepsy, Temporal Lobe - surgery</subject><subject>Female</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Hippocampus - pathology</subject><subject>Hippocampus - surgery</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Limbic System - pathology</subject><subject>Limbic System - surgery</subject><subject>Male</subject><subject>Mammillary Bodies - pathology</subject><subject>Mammillary Bodies - surgery</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neuroglia - pathology</subject><subject>Neurology</subject><subject>Neurons - pathology</subject><subject>Psychosurgery</subject><subject>Sensitivity and Specificity</subject><subject>Temporal Lobe - pathology</subject><subject>Temporal Lobe - surgery</subject><subject>Tropical medicine</subject><subject>Wallerian Degeneration - physiology</subject><issn>0028-3940</issn><issn>1432-1920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLxDAUhYMo4zi6dClkIe6qN482k40gg4-BEUF0XZL0BittU5MOOP_eimXA1V18H4dzDyHnDK4ZgLpJAFxIgBxkkR-QOZOCZ0xzOCTzES0zoSUck5OUPgFAKKFmZKa54lLDnNw-v65p8HT4QOpD7OpvarqKtqatm8bEHbWh2tG6owO2fYimoU2wSLGvG-zT7pQcedMkPJvugrw_3L-tnrLNy-N6dbfJnGBqyIw33kOeF9opYyx4x623KJjzBSIutUDvltxWBeOOgy40aGdQytwajsKLBbn6y-1j-NpiGsq2Tg7Hih2GbSqV5rLgSo1i9ie6GFKK6Ms-1u34SMmg_N2r_LfX6F9MwVvbYrW3p4FGfjlxk5xpfDSdq9Ne46qQSjDxA-KIch0</recordid><startdate>19970801</startdate><enddate>19970801</enddate><creator>NG, S. E. S</creator><creator>LAU, T. N</creator><creator>HUI, F. K. H</creator><creator>CHUA, G. E</creator><creator>LEE, W. L</creator><creator>CHEE, M. W. L</creator><creator>CHEE, T. S. G</creator><creator>BOEY, H. K</creator><general>Springer</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19970801</creationdate><title>MRI of the fornix and mamillary body in temporal lobe epilepsy</title><author>NG, S. E. S ; LAU, T. N ; HUI, F. K. H ; CHUA, G. E ; LEE, W. L ; CHEE, M. W. L ; CHEE, T. S. G ; BOEY, H. 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Cerebral palsy</topic><topic>Hippocampus - pathology</topic><topic>Hippocampus - surgery</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Limbic System - pathology</topic><topic>Limbic System - surgery</topic><topic>Male</topic><topic>Mammillary Bodies - pathology</topic><topic>Mammillary Bodies - surgery</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neuroglia - pathology</topic><topic>Neurology</topic><topic>Neurons - pathology</topic><topic>Psychosurgery</topic><topic>Sensitivity and Specificity</topic><topic>Temporal Lobe - pathology</topic><topic>Temporal Lobe - surgery</topic><topic>Tropical medicine</topic><topic>Wallerian Degeneration - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NG, S. E. S</creatorcontrib><creatorcontrib>LAU, T. N</creatorcontrib><creatorcontrib>HUI, F. K. H</creatorcontrib><creatorcontrib>CHUA, G. E</creatorcontrib><creatorcontrib>LEE, W. L</creatorcontrib><creatorcontrib>CHEE, M. W. L</creatorcontrib><creatorcontrib>CHEE, T. S. G</creatorcontrib><creatorcontrib>BOEY, H. K</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroradiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NG, S. E. S</au><au>LAU, T. N</au><au>HUI, F. K. H</au><au>CHUA, G. E</au><au>LEE, W. L</au><au>CHEE, M. W. L</au><au>CHEE, T. S. G</au><au>BOEY, H. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MRI of the fornix and mamillary body in temporal lobe epilepsy</atitle><jtitle>Neuroradiology</jtitle><addtitle>Neuroradiology</addtitle><date>1997-08-01</date><risdate>1997</risdate><volume>39</volume><issue>8</issue><spage>551</spage><epage>555</epage><pages>551-555</pages><issn>0028-3940</issn><eissn>1432-1920</eissn><coden>NRDYAB</coden><abstract>We performed MRI on 27 patients with clinically proven temporal lobe epilepsy (TLE), all with prior EEG lateralisation, and 10 volunteers, studied to evaluate disparity in size arising from biological variation (group 1). Three-dimensional spoiled GRASS (3DSPGR) sequences provided 2-mm contiguous sections of the limbic system, enabling assessment of the hippocampus (HC), fornix (FN) and mamillary body (MB). Measurements of FN and MB width were made from a workstation. Any percentage difference in size was computed. In 19 cases there was unilateral abnormality in the HC (group 2); in 18 and 19 cases respectively there was a smaller FN and MB on the same side as the abnormal HC. This percentage difference in size was significantly greater than that in group 1 in the FN and MB in 17 and 17 cases respectively. Comparison of percentage difference computations for FN and MB between groups 1 and 2 showed high statistical significance (P < 0.0002). In 5 patients with clinical TLE the HC was normal on MRI (group 3). Unequal FN and MB sizes were found in 4, significant in 2. Comparison of percentage difference computations for FN and MB showed statistical significance (P < 0.0005 and P < 0.0003 respectively). There was no case of discordance between the sides of hippocampal abnormality and the smaller FN or MB or between the sides of smaller FN and MB. The strong concordance between the changes in the HC and those in the FN and MB suggests that this combination will play an important role in the assessment of TLE and limbic system abnormality.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>9272490</pmid><doi>10.1007/s002340050465</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Child, Preschool Dominance, Cerebral - physiology Electroencephalography Epilepsy, Temporal Lobe - diagnosis Epilepsy, Temporal Lobe - pathology Epilepsy, Temporal Lobe - surgery Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Hippocampus - pathology Hippocampus - surgery Humans Image Processing, Computer-Assisted Limbic System - pathology Limbic System - surgery Male Mammillary Bodies - pathology Mammillary Bodies - surgery Medical sciences Middle Aged Nervous system (semeiology, syndromes) Neuroglia - pathology Neurology Neurons - pathology Psychosurgery Sensitivity and Specificity Temporal Lobe - pathology Temporal Lobe - surgery Tropical medicine Wallerian Degeneration - physiology |
title | MRI of the fornix and mamillary body in temporal lobe epilepsy |
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