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A new clinico-pathological classification system for mesial temporal sclerosis

We propose a histopathological classification system for hippocampal cell loss in patients suffering from mesial temporal lobe epilepsies (MTLE). One hundred and seventy-eight surgically resected specimens were microscopically examined with respect to neuronal cell loss in hippocampal subfields CA1–...

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Autores principales: Blümcke, Ingmar, Pauli, Elisabeth, Clusmann, Hans, Schramm, Johannes, Becker, Albert, Elger, Christian, Merschhemke, Martin, Meencke, Heinz-Joachim, Lehmann, Thomas, von Deimling, Andreas, Scheiwe, Christian, Zentner, Josef, Volk, Benedikt, Romstöck, Johann, Stefan, Hermann, Hildebrandt, Michelle
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794628/
https://www.ncbi.nlm.nih.gov/pubmed/17221203
http://dx.doi.org/10.1007/s00401-006-0187-0
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author Blümcke, Ingmar
Pauli, Elisabeth
Clusmann, Hans
Schramm, Johannes
Becker, Albert
Elger, Christian
Merschhemke, Martin
Meencke, Heinz-Joachim
Lehmann, Thomas
von Deimling, Andreas
Scheiwe, Christian
Zentner, Josef
Volk, Benedikt
Romstöck, Johann
Stefan, Hermann
Hildebrandt, Michelle
author_facet Blümcke, Ingmar
Pauli, Elisabeth
Clusmann, Hans
Schramm, Johannes
Becker, Albert
Elger, Christian
Merschhemke, Martin
Meencke, Heinz-Joachim
Lehmann, Thomas
von Deimling, Andreas
Scheiwe, Christian
Zentner, Josef
Volk, Benedikt
Romstöck, Johann
Stefan, Hermann
Hildebrandt, Michelle
author_sort Blümcke, Ingmar
collection PubMed
description We propose a histopathological classification system for hippocampal cell loss in patients suffering from mesial temporal lobe epilepsies (MTLE). One hundred and seventy-eight surgically resected specimens were microscopically examined with respect to neuronal cell loss in hippocampal subfields CA1–CA4 and dentate gyrus. Five distinct patterns were recognized within a consecutive cohort of anatomically well-preserved surgical specimens. The first group comprised hippocampi with neuronal cell densities not significantly different from age matched autopsy controls [no mesial temporal sclerosis (no MTS); n = 34, 19%]. A classical pattern with severe cell loss in CA1 and moderate neuronal loss in all other subfields excluding CA2 was observed in 33 cases (19%), whereas the vast majority of cases showed extensive neuronal cell loss in all hippocampal subfields (n = 94, 53%). Due to considerable similarities of neuronal cell loss patterns and clinical histories, we designated these two groups as MTS type 1a and 1b, respectively. We further distinguished two atypical variants characterized either by severe neuronal loss restricted to sector CA1 (MTS type 2; n = 10, 6%) or to the hilar region (MTS type 3, n = 7, 4%). Correlation with clinical data pointed to an early age of initial precipitating injury (IPI < 3 years) as important predictor of hippocampal pathology, i.e. MTS type 1a and 1b. In MTS type 2, IPIs were documented at a later age (mean 6 years), whereas in MTS type 3 and normal appearing hippocampus (no MTS) the first event appeared beyond the age of 13 and 16 years, respectively. In addition, postsurgical outcome was significantly worse in atypical MTS, especially MTS type 3 with only 28% of patients having seizure relief after 1-year follow-up period, compared to successful seizure control in MTS types 1a and 1b (72 and 73%). Our classification system appears suitable for stratifying the clinically heterogeneous group of MTLE patients also with respect to postsurgical outcome studies.
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spelling pubmed-17946282007-02-08 A new clinico-pathological classification system for mesial temporal sclerosis Blümcke, Ingmar Pauli, Elisabeth Clusmann, Hans Schramm, Johannes Becker, Albert Elger, Christian Merschhemke, Martin Meencke, Heinz-Joachim Lehmann, Thomas von Deimling, Andreas Scheiwe, Christian Zentner, Josef Volk, Benedikt Romstöck, Johann Stefan, Hermann Hildebrandt, Michelle Acta Neuropathol Original Paper We propose a histopathological classification system for hippocampal cell loss in patients suffering from mesial temporal lobe epilepsies (MTLE). One hundred and seventy-eight surgically resected specimens were microscopically examined with respect to neuronal cell loss in hippocampal subfields CA1–CA4 and dentate gyrus. Five distinct patterns were recognized within a consecutive cohort of anatomically well-preserved surgical specimens. The first group comprised hippocampi with neuronal cell densities not significantly different from age matched autopsy controls [no mesial temporal sclerosis (no MTS); n = 34, 19%]. A classical pattern with severe cell loss in CA1 and moderate neuronal loss in all other subfields excluding CA2 was observed in 33 cases (19%), whereas the vast majority of cases showed extensive neuronal cell loss in all hippocampal subfields (n = 94, 53%). Due to considerable similarities of neuronal cell loss patterns and clinical histories, we designated these two groups as MTS type 1a and 1b, respectively. We further distinguished two atypical variants characterized either by severe neuronal loss restricted to sector CA1 (MTS type 2; n = 10, 6%) or to the hilar region (MTS type 3, n = 7, 4%). Correlation with clinical data pointed to an early age of initial precipitating injury (IPI < 3 years) as important predictor of hippocampal pathology, i.e. MTS type 1a and 1b. In MTS type 2, IPIs were documented at a later age (mean 6 years), whereas in MTS type 3 and normal appearing hippocampus (no MTS) the first event appeared beyond the age of 13 and 16 years, respectively. In addition, postsurgical outcome was significantly worse in atypical MTS, especially MTS type 3 with only 28% of patients having seizure relief after 1-year follow-up period, compared to successful seizure control in MTS types 1a and 1b (72 and 73%). Our classification system appears suitable for stratifying the clinically heterogeneous group of MTLE patients also with respect to postsurgical outcome studies. Springer-Verlag 2007-01-13 2007-03 /pmc/articles/PMC1794628/ /pubmed/17221203 http://dx.doi.org/10.1007/s00401-006-0187-0 Text en © Springer-Verlag 2007
spellingShingle Original Paper
Blümcke, Ingmar
Pauli, Elisabeth
Clusmann, Hans
Schramm, Johannes
Becker, Albert
Elger, Christian
Merschhemke, Martin
Meencke, Heinz-Joachim
Lehmann, Thomas
von Deimling, Andreas
Scheiwe, Christian
Zentner, Josef
Volk, Benedikt
Romstöck, Johann
Stefan, Hermann
Hildebrandt, Michelle
A new clinico-pathological classification system for mesial temporal sclerosis
title A new clinico-pathological classification system for mesial temporal sclerosis
title_full A new clinico-pathological classification system for mesial temporal sclerosis
title_fullStr A new clinico-pathological classification system for mesial temporal sclerosis
title_full_unstemmed A new clinico-pathological classification system for mesial temporal sclerosis
title_short A new clinico-pathological classification system for mesial temporal sclerosis
title_sort new clinico-pathological classification system for mesial temporal sclerosis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1794628/
https://www.ncbi.nlm.nih.gov/pubmed/17221203
http://dx.doi.org/10.1007/s00401-006-0187-0
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