Extended resection for seizure control of pure motor strip focal cortical dysplasia during awake craniotomy: illustrative case.

awake craniotomy brain mapping epilepsy surgery focal cortical dysplasia

Journal

Journal of neurosurgery. Case lessons
ISSN: 2694-1902
Titre abrégé: J Neurosurg Case Lessons
Pays: United States
ID NLM: 9918227275606676

Informations de publication

Date de publication:
07 Mar 2022
Historique:
received: 21 10 2021
accepted: 03 01 2022
entrez: 21 9 2022
pubmed: 22 9 2022
medline: 22 9 2022
Statut: epublish

Résumé

Focal cortical dysplasias (FCD) represent highly intrinsically epileptogenic lesions that require complete resection for seizure control. Resection of pure motor strip FCD can be challenging. Effective control of postoperative seizures is crucial and extending the boundaries of resection in an eloquent zone remains controversial. The authors report a 52-year-old right-handed male with refractory epilepsy. The seizure phenotype was a focal crisis with preserved awareness and a clonic motor onset of right-hemibody. Epilepsy surgery protocol demonstrated a left pure motor strip FCD and a full-awake resective procedure with motor brain mapping was performed. Further resection of surgical boundaries monitoring function along intraoperative motor tasks with no direct electrical stimulation corroborated by intraoperative-neuromonitorization was completed as the final part of the surgery. In the follow-up period of 3-years, the patient has an Engel-IB seizure-control with mild distal lower limb palsy and no gate compromise. This report represents one of the few cases with pure motor strip FCD resection. In a scenario similar to this case, the authors consider that this variation can be useful to improve seizure control and the quality of life of these patients by extending the resection of a more extensive epileptogenic zone minimizing functional damage.

Sections du résumé

BACKGROUND BACKGROUND
Focal cortical dysplasias (FCD) represent highly intrinsically epileptogenic lesions that require complete resection for seizure control. Resection of pure motor strip FCD can be challenging. Effective control of postoperative seizures is crucial and extending the boundaries of resection in an eloquent zone remains controversial.
OBSERVATIONS METHODS
The authors report a 52-year-old right-handed male with refractory epilepsy. The seizure phenotype was a focal crisis with preserved awareness and a clonic motor onset of right-hemibody. Epilepsy surgery protocol demonstrated a left pure motor strip FCD and a full-awake resective procedure with motor brain mapping was performed. Further resection of surgical boundaries monitoring function along intraoperative motor tasks with no direct electrical stimulation corroborated by intraoperative-neuromonitorization was completed as the final part of the surgery. In the follow-up period of 3-years, the patient has an Engel-IB seizure-control with mild distal lower limb palsy and no gate compromise.
LESSONS CONCLUSIONS
This report represents one of the few cases with pure motor strip FCD resection. In a scenario similar to this case, the authors consider that this variation can be useful to improve seizure control and the quality of life of these patients by extending the resection of a more extensive epileptogenic zone minimizing functional damage.

Identifiants

pubmed: 36130534
doi: 10.3171/CASE21605
pii: CASE21605
pmc: PMC9379631
doi:
pii:

Types de publication

Journal Article

Langues

eng

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Auteurs

Bayron A Sandoval-Bonilla (BA)

1Department of Neurosurgery, Epilepsy Surgery Program, Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

André Palmini (A)

2Department of Neurology and Neurosurgery, Epilepsy Surgery Program, Hospital São Lucas da Pontificia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil.

Eliseu Paglioli (E)

2Department of Neurology and Neurosurgery, Epilepsy Surgery Program, Hospital São Lucas da Pontificia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil.

Alejandro Monroy-Sosa (A)

3Department of Neurosurgery, Aurora Neuroscience Innovation Institute, Aurora St. Luke's Medical Center, Milwaukee, Wisconsin.
4Skull Base, Brain & Cerebrovascular Laboratory, Advocate Aurora Research Health Institute, Milwaukee, Wisconsin.

Maria F De la Cerda-Vargas (MF)

5Department of Neurosurgery, Hospital de Especialidades No. 71, Instituto Mexicano del Seguro Social, Torreón Coahuila, Mexico.

Job J Rodríguez-Hernández (JJ)

1Department of Neurosurgery, Epilepsy Surgery Program, Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

Victor R Chávez-Herrera (VR)

1Department of Neurosurgery, Epilepsy Surgery Program, Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

Sara P Perez-Reyes (SP)

6Department of Neurosurgery, Hospital Regional de Alta Especialidad del Bajío, Instituto Mexicano del Seguro Social, Leon, Guanajuato, Mexico.

Fernando C Castro-Prado (FC)

1Department of Neurosurgery, Epilepsy Surgery Program, Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
7Department of Neurosurgery, High Specialties Regional Hospital Gral. I. Zaragoza, ISSSTE, Mexico City, Mexico.

Samuel Perez-Cardenas (S)

8Department of Neurosurgery, University Hospital Monterrey, Nuevo Leon, Mexico; and.

Josafat J Sánchez-Dueñas (JJ)

1Department of Neurosurgery, Epilepsy Surgery Program, Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.

Lucero N Lagunes-Padilla (LN)

9Department of Neurosurgery, Hospital Angeles Universidad, Mexico City, Mexico.

Classifications MeSH