Multinodular and vacuolating neuronal tumor in the thalamus: case report and systematic review of literature
Document Type
Article
Abstract
The authors present the first reported case of MVNT in the thalamus in a 60-year-old man with a 20-year history of epilepsy and recent progressive neurological decline presented for neurosurgical evaluation for a non-enhancing mass predominantly in the right thalamus presumed to be a low-grade glioma. The tumor was subtotally resected using a left contralateral interhemispheric transcallosal approach. Histological and molecular assessment revealed an MVNT with MAPK pathway-activating mutation. The authors also conducted a systematic review of pathology-proven cases of MVNT to provide an up-to-date overview of the literature on the localization, presenting symptoms, and recurrence of this tumor.
Medical Subject Headings
Humans; Male; Middle Aged; Brain Neoplasms (surgery, pathology, diagnostic imaging); Glioma (surgery, pathology, diagnostic imaging); Thalamus (pathology, surgery, diagnostic imaging); Diagnosis, Differential
Publication Date
8-19-2024
Publication Title
Acta neurochirurgica
E-ISSN
0942-0940
Volume
166
Issue
1
First Page
340
PubMed ID
39160266
Digital Object Identifier (DOI)
10.1007/s00701-024-06230-8
Recommended Citation
On, Thomas J.; Alcantar-Garibay, Oscar; Xu, Yuan; Abramov, Irakliy; Eschbacher, Jennifer M.; Tiwari, Nishant; Smith, Kris A.; and Preul, Mark C., "Multinodular and vacuolating neuronal tumor in the thalamus: case report and systematic review of literature" (2024). Neurosurgery. 2341.
https://scholar.barrowneuro.org/neurosurgery/2341