The Role of FDG-PET in Patients with Epilepsy Related to Periventricular Nodular Heterotopias: Diagnostic Features and Long-Term Outcome.


Journal

Journal of neuroimaging : official journal of the American Society of Neuroimaging
ISSN: 1552-6569
Titre abrégé: J Neuroimaging
Pays: United States
ID NLM: 9102705

Informations de publication

Date de publication:
07 2019
Historique:
received: 29 11 2018
revised: 01 04 2019
accepted: 04 04 2019
pubmed: 23 4 2019
medline: 17 6 2020
entrez: 23 4 2019
Statut: ppublish

Résumé

Periventricular nodular heterotopias (PNHs) are frequently associated with drug-resistant epilepsy (DRE). Although magnetic resonance imaging (MRI) can define the morphological features of PNHs, still there is a need to assess their metabolic activity in order to provide useful information on epileptogenicity and long-term outcome. To that end, we investigated the ability of Sixteen patients (6 men and 10 women; ranging between 24 and 53 years of age) with PNHs-related DRE were evaluated. All patients underwent clinical evaluation, Stereo-electroencephalogram (SEEG), brain MRI, and Thirty-one heterotopic sites were identified. Twenty-one of 23 nodules with detectable electric activity on SEEG were identified by PET (91.3%), while 5 of 8 of nodules without electric activity showed no metabolism on PET (62.5%). Overall, the concordance between SEEG and FDG-PET was 26/31 (83.9%). Furthermore, cortical metabolic alterations were depicted, correlating with epileptogenic areas. A favorable postsurgical outcome was reported in 13 patients (81.3%). The presence of a hypometabolic nodule significantly correlated with a worse outcome after surgical therapy (P = .036). In PNHs-related epilepsy, FDG-PET more accurately identifies epileptogenic foci, which aids surgical planning and in postoperative seizure control.

Sections du résumé

BACKGROUND AND PURPOSE
Periventricular nodular heterotopias (PNHs) are frequently associated with drug-resistant epilepsy (DRE). Although magnetic resonance imaging (MRI) can define the morphological features of PNHs, still there is a need to assess their metabolic activity in order to provide useful information on epileptogenicity and long-term outcome. To that end, we investigated the ability of
METHODS
Sixteen patients (6 men and 10 women; ranging between 24 and 53 years of age) with PNHs-related DRE were evaluated. All patients underwent clinical evaluation, Stereo-electroencephalogram (SEEG), brain MRI, and
RESULTS
Thirty-one heterotopic sites were identified. Twenty-one of 23 nodules with detectable electric activity on SEEG were identified by PET (91.3%), while 5 of 8 of nodules without electric activity showed no metabolism on PET (62.5%). Overall, the concordance between SEEG and FDG-PET was 26/31 (83.9%). Furthermore, cortical metabolic alterations were depicted, correlating with epileptogenic areas. A favorable postsurgical outcome was reported in 13 patients (81.3%). The presence of a hypometabolic nodule significantly correlated with a worse outcome after surgical therapy (P = .036).
CONCLUSIONS
In PNHs-related epilepsy, FDG-PET more accurately identifies epileptogenic foci, which aids surgical planning and in postoperative seizure control.

Identifiants

pubmed: 31006947
doi: 10.1111/jon.12620
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

512-520

Informations de copyright

© 2019 by the American Society of Neuroimaging.

Auteurs

Cristina Elena Popescu (CE)

Nuclear Medicine Department, Niguarda Hospital, Milan, Italy.

Roberto Mai (R)

Epilepsy Surgery Centre, Niguarda Hospital, Milan, Italy.

Roberto Sara (R)

Nuclear Medicine Department, Niguarda Hospital, Milan, Italy.

Domenico Lizio (D)

Medical Physics Unit, Niguarda Hospital, Milan, Italy.

Daniela Zanni (D)

Medical Physics Unit, Niguarda Hospital, Milan, Italy.

Claudio Rossetti (C)

Nuclear Medicine Department, Niguarda Hospital, Milan, Italy.

Federico Caobelli (F)

Clinic of Radiology & Nuclear Medicine, University Hospital Basel, University of Basel, Basel, Switzerland.

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