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69. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
Joint Meeting mit der Mexikanischen und Kolumbianischen Gesellschaft für Neurochirurgie

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

03.06. - 06.06.2018, Münster

Corpus callosotomy in pediatricdrug resistent lesionalepilepsies – diagnostic approach or therapeutic option?

Meeting Abstract

  • Manfred Kudernatsch - Schön Klinik Vogtareuth, Klinik für Neurochirurgie und Epilepsiechirurgie, Vogtareuth, Deutschland
  • Till Hartlieb - Schön Klinik Vogtareuth, Neuropädiatrie, Vogtareuth, Deutschland
  • Manfred Kudernatsch - Schön Klinik Vogtareuth, Klinik für Neurochirurgie und Epilepsiechirurgie, Vogtareuth, Deutschland
  • Tom Pieper - Schön Klinik Vogtareuth, Neuropädiatrie, Vogtareuth, Deutschland
  • Martin Staudt - Schön Klinik Vogtareuth, Neuropädiatrie, Vogtareuth, Deutschland; Universitätsklinik für Kinder- und Jugendmedizin, Abteilung Neuropädiatrie und Entwicklungsneurologie, Tübingen, Deutschland
  • Hans Holthausen - Schön Klinik Vogtareuth, Neuropädiatrie, Vogtareuth, Deutschland
  • Peter A. Winkler - Schön Klinik Vogtareuth, Neuropädiatrie, Vogtareuth, Deutschland
  • Ingmar Blümcke - Universitätsklinik Erlangen, Neurochirurgische Klinik, Erlangen, Deutschland

Deutsche Gesellschaft für Neurochirurgie. 69. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), Joint Meeting mit der Mexikanischen und Kolumbianischen Gesellschaft für Neurochirurgie. Münster, 03.-06.06.2018. Düsseldorf: German Medical Science GMS Publishing House; 2018. DocV178

doi: 10.3205/18dgnc181, urn:nbn:de:0183-18dgnc1814

Published: June 18, 2018

© 2018 Kudernatsch et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

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Objective: CC in our 12 pts led to postoperative EEG lateralization and recommendation to 2nd surgery in 6 cases. In 3 cases 2nd resective surgery was performed with seizure freedom in one and favorable outcome in 2 patients. Quality of life was improved in 9 cases after CC, therefore 3 pts still waiting for 2nd resective surgeryin case of future aggravation of epilepsy. None of the patients showed negative effects after CC. CC can be a helpful tool in diagnostic work-up of pts with focal epilepsies and bilateral findings in order to provide further surgical treatment options. Regarding quality of life CC is a serious treatment option for selected pts with medically intractable lesional epilepsies.

Methods: 12 pts (f:3; m:9). All severely mentally retarded. Etiology: malformation of cortical development (8), PMG (2), HHE-syndrome (1), herpes encephalitis (1). Bilateral EEG (12/12), bilateral pathology in hrMRI (6/12). Postoperative EEG lateralization (6/12), recommendation to 2nd resective surgery (6/12) 2nd resective surgery performed (3/12): t-p-o resection(1), hemispherotomy(2). Significant improvement of quality of daily life regarding alertness and participation (9/12). Post CC ventriculo-peritoneal shunt was required in 1 pt.

Results: Out of 600 patients who underwent epilepsy surgery between 09/1998 and 11/2017 at the Epilepsy Center for Children and Adolescents, retrospective data of 12 CC patients are presented. All underwent video-EEG long-term monitoring at least once and high resolution MRI. Presurgical diagnostic work up including genetic testing ruled out etiologies other than focal lesional epilepsies.

Conclusion: Epilepsy surgery is a successful treatment option for children with drug resistant lesional epilepsies. Age dependent bilateral/generalized EEG-findings and non lateralizing semiology may blur the electro-clinico-anatomical correlation, which is crucial for successful surgical approach. Rapid lateralization and localization of the epileptogenic zone (EZ) is required in case of high seizure burden and/or developmental delayor cognitive decline. In 12 children with either unilateral lesion and poor electro-clinical-anatomical correlation or suspected bilateral lesion and bilateral EEG we performed a corpus callosotomy (CC) as diagnostic approach to lateralize the EZ.