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Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy

OBJECTIVE: Transsylvian selective amygdalo‐hippocampectomy (tsSAHE) represents a generally recognized surgical procedure for drug‐resistant mesial temporal lobe epilepsy (mTLE). Although postoperative seizure freedom can be achieved in about 70% of tsSAHE, there is a considerable amount of patients...

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Autores principales: Borger, Valeri, Schneider, Matthias, Taube, Julia, Potthoff, Anna‐Laura, Keil, Vera C., Hamed, Motaz, Aydin, Gülsah, Ilic, Inja, Solymosi, László, Elger, Christian E., Güresir, Erdem, Fimmers, Rolf, Schuss, Patrick, Helmstaedter, Christoph, Surges, Rainer, Vatter, Hartmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818082/
https://www.ncbi.nlm.nih.gov/pubmed/33263942
http://dx.doi.org/10.1002/acn3.51263
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author Borger, Valeri
Schneider, Matthias
Taube, Julia
Potthoff, Anna‐Laura
Keil, Vera C.
Hamed, Motaz
Aydin, Gülsah
Ilic, Inja
Solymosi, László
Elger, Christian E.
Güresir, Erdem
Fimmers, Rolf
Schuss, Patrick
Helmstaedter, Christoph
Surges, Rainer
Vatter, Hartmut
author_facet Borger, Valeri
Schneider, Matthias
Taube, Julia
Potthoff, Anna‐Laura
Keil, Vera C.
Hamed, Motaz
Aydin, Gülsah
Ilic, Inja
Solymosi, László
Elger, Christian E.
Güresir, Erdem
Fimmers, Rolf
Schuss, Patrick
Helmstaedter, Christoph
Surges, Rainer
Vatter, Hartmut
author_sort Borger, Valeri
collection PubMed
description OBJECTIVE: Transsylvian selective amygdalo‐hippocampectomy (tsSAHE) represents a generally recognized surgical procedure for drug‐resistant mesial temporal lobe epilepsy (mTLE). Although postoperative seizure freedom can be achieved in about 70% of tsSAHE, there is a considerable amount of patients with persisting postoperative seizures. This might partly be explained by differing extents of resection of various tsSAHE target volumes. In this study we analyzed the resected proportions of hippocampus, amygdala as well as piriform cortex in regard of postoperative seizure outcome. METHODS: Between 2012 and 2017, 82 of 103 patients with mTLE who underwent tsSAHE at the authors’ institution were included in the analysis. Resected proportions of hippocampus, amygdala and temporal piriform cortex as target structures of tsSAHE were volumetrically assessed and stratified according to favorable (International League Against Epilepsy (ILAE) class 1) and unfavorable (ILAE class 2–6) seizure outcome. RESULTS: Patients with favorable seizure outcome revealed a significantly larger proportion of resected temporal piriform cortex volumes compared to patients with unfavorable seizure outcome (median resected proportional volumes were 51% (IQR 42–61) versus (vs.) 13 (IQR 11–18), P = 0.0001). Resected proportions of hippocampus and amygdala did not significantly differ for these groups (hippocampus: 81% (IQR 73–88) vs. 80% (IQR 74–92) (P = 0.7); amygdala: 100% (IQR 100–100) vs. 100% (IQR 100–100) (P = 0.7)). INTERPRETATION: These results strongly suggest temporal piriform cortex to constitute a key target resection volume to achieve seizure freedom following tsSAHE.
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spelling pubmed-78180822021-01-29 Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy Borger, Valeri Schneider, Matthias Taube, Julia Potthoff, Anna‐Laura Keil, Vera C. Hamed, Motaz Aydin, Gülsah Ilic, Inja Solymosi, László Elger, Christian E. Güresir, Erdem Fimmers, Rolf Schuss, Patrick Helmstaedter, Christoph Surges, Rainer Vatter, Hartmut Ann Clin Transl Neurol Research Articles OBJECTIVE: Transsylvian selective amygdalo‐hippocampectomy (tsSAHE) represents a generally recognized surgical procedure for drug‐resistant mesial temporal lobe epilepsy (mTLE). Although postoperative seizure freedom can be achieved in about 70% of tsSAHE, there is a considerable amount of patients with persisting postoperative seizures. This might partly be explained by differing extents of resection of various tsSAHE target volumes. In this study we analyzed the resected proportions of hippocampus, amygdala as well as piriform cortex in regard of postoperative seizure outcome. METHODS: Between 2012 and 2017, 82 of 103 patients with mTLE who underwent tsSAHE at the authors’ institution were included in the analysis. Resected proportions of hippocampus, amygdala and temporal piriform cortex as target structures of tsSAHE were volumetrically assessed and stratified according to favorable (International League Against Epilepsy (ILAE) class 1) and unfavorable (ILAE class 2–6) seizure outcome. RESULTS: Patients with favorable seizure outcome revealed a significantly larger proportion of resected temporal piriform cortex volumes compared to patients with unfavorable seizure outcome (median resected proportional volumes were 51% (IQR 42–61) versus (vs.) 13 (IQR 11–18), P = 0.0001). Resected proportions of hippocampus and amygdala did not significantly differ for these groups (hippocampus: 81% (IQR 73–88) vs. 80% (IQR 74–92) (P = 0.7); amygdala: 100% (IQR 100–100) vs. 100% (IQR 100–100) (P = 0.7)). INTERPRETATION: These results strongly suggest temporal piriform cortex to constitute a key target resection volume to achieve seizure freedom following tsSAHE. John Wiley and Sons Inc. 2020-12-02 /pmc/articles/PMC7818082/ /pubmed/33263942 http://dx.doi.org/10.1002/acn3.51263 Text en © 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Borger, Valeri
Schneider, Matthias
Taube, Julia
Potthoff, Anna‐Laura
Keil, Vera C.
Hamed, Motaz
Aydin, Gülsah
Ilic, Inja
Solymosi, László
Elger, Christian E.
Güresir, Erdem
Fimmers, Rolf
Schuss, Patrick
Helmstaedter, Christoph
Surges, Rainer
Vatter, Hartmut
Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title_full Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title_fullStr Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title_full_unstemmed Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title_short Resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
title_sort resection of piriform cortex predicts seizure freedom in temporal lobe epilepsy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818082/
https://www.ncbi.nlm.nih.gov/pubmed/33263942
http://dx.doi.org/10.1002/acn3.51263
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