Glioblastoma after deep brain stimulation: a case report and literature review

Abstract Background Deep brain stimulation (DBS) is an established treatment for movement disorders, whereas glioblastoma is the most common malignant primary brain tumor. Their coexistence is rarely reported. Objective To report a case of glioblastoma developing after DBS and review the literature. Methods A 64-year-old man developed glioblastoma 2 years after bilateral subthalamic nucleus (STN) DBS for Parkinson’s disease. A literature review was performed using PubMed and Google Scholar. Results Only seven similar cases have been reported. Although no evidence supports a causal relationship between DBS and tumor formation, optimal management remains unclear. Conclusion Further studies are needed to clarify any association between chronic electrical stimulation and tumor development. New atypical neurological deficits in DBS patients should prompt neuroimaging. Multidisciplinary management is essential.

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Publication Details

Journal
The Egyptian Journal of Neurosurgery : the official publication of the Egyptian Society of Neurological Surgeons/Egyptian journal of neurosurgery
Published
2026-09-10
DOI
https://doi.org/10.1186/s41984-026-00659-y
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Glioblastoma after deep brain stimulation: a case report and literature review

Mansour Parvaresh, Alireza Mohsenian Sisakht, Seyed Amir Hassan Habibi, Alfonso Fasano et al.
The Egyptian Journal of Neurosurgery : the official publication of the Egyptian Society of Neurological Surgeons/Egyptian journal of neurosurgery
Neurological disorders and treatments
article

Glioblastoma after deep brain stimulation: a case report and literature review

Mansour Parvaresh, Alireza Mohsenian Sisakht, Seyed Amir Hassan Habibi, Alfonso Fasano, Mohamad Rohani
article en

Abstract

Abstract Background Deep brain stimulation (DBS) is an established treatment for movement disorders, whereas glioblastoma is the most common malignant primary brain tumor. Their coexistence is rarely reported. Objective To report a case of glioblastoma developing after DBS and review the literature. Methods A 64-year-old man developed glioblastoma 2 years after bilateral subthalamic nucleus (STN) DBS for Parkinson’s disease. A literature review was performed using PubMed and Google Scholar. Results Only seven similar cases have been reported. Although no evidence supports a causal relationship between DBS and tumor formation, optimal management remains unclear. Conclusion Further studies are needed to clarify any association between chronic electrical stimulation and tumor development. New atypical neurological deficits in DBS patients should prompt neuroimaging. Multidisciplinary management is essential.

The Egyptian Journal of Neurosurgery : the official publication of the Egyptian Society of Neurological Surgeons/Egyptian journal of neurosurgeryVol. 41(1)
Humanitas University (IT), Iran University of Medical Sciences (IR), Rasool Akram Hospital (IR), IRCCS Humanitas Research Hospital (IT)
Good health and well-being
Openalex Percentile: Top 11%
Neurological disorders and treatments
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