Longitudinal radiological follow-up of individual level non-ischemic cerebral enhancing lesions following endovascular aneurysm treatment

Author:

Guetarni ZakariaORCID,Bernard Remy,Boulouis Grégoire,Labeyrie Marc-Antoine,Biondi AlessandraORCID,Velasco Stéphane,Saliou GuillaumeORCID,Bartolini BrunoORCID,Daumas-Duport Benjamin,Bourcier Romain,Janot KevinORCID,Herbreteau Denis,Michelozzi Caterina,Premat Kevin,Redjem Hocine,Escalard SimonORCID,Bricout NicolasORCID,Thouant Pierre,Arteaga Charles,Pierot LaurentORCID,Tahon Florence,Boubagra KamelORCID,Ikka Leon,Chabert Emmanuel,Lenck Stephanie,Guédon Alexis,Consoli Arturo,Saleme Suzana,Forestier GéraudORCID,Di Maria Federico,Ferré Jean-Christophe,Anxionnat RenéORCID,Eugene FrancoisORCID,Kerleroux BasileORCID,Dargazanli Cyril,Sourour Nader-Antoine,Clarençon Frédéric,Shotar Eimad

Abstract

BackgroundNon-ischemic cerebral enhancing (NICE) lesions following aneurysm endovascular therapy are exceptionally rare, with unknown longitudinal evolution.ObjectiveTo evaluate the radiological behavior of individual NICE lesions over time.MethodsPatients included in a retrospective national multicentric inception cohort were analyzed. NICE lesions were defined, using MRI, as delayed onset punctate, nodular, or annular foci enhancements with peri-lesion edema, distributed in the vascular territory of the aneurysm treatment, with no other confounding disease. Lesion burden and the longitudinal behavior of individual lesions were assessed.ResultsTwenty-two patients were included, with a median initial lesion burden of 36 (IQR 17–54) on the first MRI scan. Of the 22 patients with at least one follow-up MRI scan, 16 (73%) had new lesions occurring mainly within the first 200 weeks after the date of the procedure. The median number of new lesions per MRI was 6 (IQR 2–16). Among the same 22 patients, 7 (32%) had recurrent lesions. The median persistent enhancement of a NICE lesion was 13 weeks (IQR 6–30). No factor was predictive of early regression of enhancement activity with lesion regression kinetics mainly being patient-dependent.ConclusionsThe behavior of individual NICE lesions was found to be highly variable with an overall patient-dependent regression velocity.

Publisher

BMJ

Subject

Neurology (clinical),General Medicine,Surgery

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