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Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis
OBJECTIVE: To analyse the surgical outcomes of pediatric patients with Lennox-Gastaut syndrome (LGS) secondary to viral encephalitis. METHODS: We retrospectively analyzed the data of four patients with LGS secondary to viral encephalitis who underwent surgery at the pediatric epilepsy center of Peki...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998939/ https://www.ncbi.nlm.nih.gov/pubmed/36908602 http://dx.doi.org/10.3389/fneur.2023.1097535 |
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author | Liu, Qingzhu Wu, Nan Liu, Chang Yu, Hao Sun, Yu Wang, Yao Yu, Guojing Wang, Shuang Ji, Taoyun Liu, Xiaoyan Jiang, Yuwu Cai, Lixin |
author_facet | Liu, Qingzhu Wu, Nan Liu, Chang Yu, Hao Sun, Yu Wang, Yao Yu, Guojing Wang, Shuang Ji, Taoyun Liu, Xiaoyan Jiang, Yuwu Cai, Lixin |
author_sort | Liu, Qingzhu |
collection | PubMed |
description | OBJECTIVE: To analyse the surgical outcomes of pediatric patients with Lennox-Gastaut syndrome (LGS) secondary to viral encephalitis. METHODS: We retrospectively analyzed the data of four patients with LGS secondary to viral encephalitis who underwent surgery at the pediatric epilepsy center of Peking University First Hospital from January 2014 to December 2019. Preoperative evaluations included a detailed history, long-term video electroencephalography (VEEG), brain magnetic resonance imaging (MRI), positron emission tomography (PET) and a neuropsychological test. All patients were followed up at 1, 3, and 6 months and then yearly. The surgical outcome was evaluated according to the Engel classification. RESULTS: Among the four children, the surgeries were right temporo-parieto-occipital disconnection (case 1), corpus callosotomy (case 2), left temporo-parieto-occipital disconnection (case 3), and left temporal lobectomy (case 4). The pathology was gliosis secondary to viral encephalitis. The median follow-up time was 4 years (3–5 years). At the last follow-up, one case had Engel I, two cases had Engel III, and one case had Engel IV. CONCLUSIONS: Preliminary observations shows that surgical treatment may be challenging for patients with LGS secondary to viral encephalitis. However, suitable surgical candidacy and approaches have a significant impact on the prognosis of the patients. |
format | Online Article Text |
id | pubmed-9998939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99989392023-03-11 Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis Liu, Qingzhu Wu, Nan Liu, Chang Yu, Hao Sun, Yu Wang, Yao Yu, Guojing Wang, Shuang Ji, Taoyun Liu, Xiaoyan Jiang, Yuwu Cai, Lixin Front Neurol Neurology OBJECTIVE: To analyse the surgical outcomes of pediatric patients with Lennox-Gastaut syndrome (LGS) secondary to viral encephalitis. METHODS: We retrospectively analyzed the data of four patients with LGS secondary to viral encephalitis who underwent surgery at the pediatric epilepsy center of Peking University First Hospital from January 2014 to December 2019. Preoperative evaluations included a detailed history, long-term video electroencephalography (VEEG), brain magnetic resonance imaging (MRI), positron emission tomography (PET) and a neuropsychological test. All patients were followed up at 1, 3, and 6 months and then yearly. The surgical outcome was evaluated according to the Engel classification. RESULTS: Among the four children, the surgeries were right temporo-parieto-occipital disconnection (case 1), corpus callosotomy (case 2), left temporo-parieto-occipital disconnection (case 3), and left temporal lobectomy (case 4). The pathology was gliosis secondary to viral encephalitis. The median follow-up time was 4 years (3–5 years). At the last follow-up, one case had Engel I, two cases had Engel III, and one case had Engel IV. CONCLUSIONS: Preliminary observations shows that surgical treatment may be challenging for patients with LGS secondary to viral encephalitis. However, suitable surgical candidacy and approaches have a significant impact on the prognosis of the patients. Frontiers Media S.A. 2023-02-24 /pmc/articles/PMC9998939/ /pubmed/36908602 http://dx.doi.org/10.3389/fneur.2023.1097535 Text en Copyright © 2023 Liu, Wu, Liu, Yu, Sun, Wang, Yu, Wang, Ji, Liu, Jiang and Cai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Liu, Qingzhu Wu, Nan Liu, Chang Yu, Hao Sun, Yu Wang, Yao Yu, Guojing Wang, Shuang Ji, Taoyun Liu, Xiaoyan Jiang, Yuwu Cai, Lixin Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title | Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title_full | Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title_fullStr | Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title_full_unstemmed | Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title_short | Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis |
title_sort | pediatric epilepsy surgery in patients with lennox-gastaut syndrome after viral encephalitis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998939/ https://www.ncbi.nlm.nih.gov/pubmed/36908602 http://dx.doi.org/10.3389/fneur.2023.1097535 |
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