Autoimmune Encephalitis-like Presentation of Glioblastoma: Get to Know This Rare Occurrence

<b>Background</b>: Glioblastoma (GBM) is the most common primary brain tumor in adults, with a poor prognosis and survival. Although typically presenting with focal neurological deficits, seizures, or cognitive decline, GBM can occasionally mimic autoimmune encephalitis (AE), leading to significant diagnostic delay. The overlap in clinical, radiological, and serological findings between GBM and AE underscores the need for thorough evaluation. <b>Methods</b>: We retrospectively reviewed cases of patients diagnosed between 2016 and 2023 with pathology-confirmed GBM, critically rethinking those cases initially diagnosed with AE at symptom onset. The diagnostic workup included magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, autoantibody testing, and whole-body nuclear scanning to exclude extracranial malignancies. <b>Results</b>: We found five female patients diagnosed with GBM who initially presented with signs and symptoms suggestive for AE. Initial MRI showed non-specific brain tissue alterations, without definitive tumor features. CSF analysis was largely unremarkable, though some cases exhibited positive autoantibodies. Despite therapy, clinical deterioration and follow-up MRI revealed infiltrative intra-axial lesions with contrast enhancement, leading to pathology-confirmed GBM diagnoses. All patients had poor prognoses, with a mean survival of 10 ± 4 months. <b>Conclusions</b>: GBM can mimic AE, delaying appropriate treatment. In patients with atypical MRI findings and suboptimal response to therapy, early follow-up imaging and biopsy should be considered to exclude malignancy. A multidisciplinary approach is critical for timely diagnosis and improved management.

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Publication Details

Journal
Journal of Clinical Medicine
Published
2025-05-29
DOI
https://doi.org/10.3390/jcm14113807
Citations
4
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
Field-Weighted Citation Impact
5.56
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article

Autoimmune Encephalitis-like Presentation of Glioblastoma: Get to Know This Rare Occurrence

Mario Tortora, Andrea Elefante, Camilla Russo, Vincenzo D’Agostino et al.
4 citations
Journal of Clinical Medicine
Autoimmune Neurological Disorders and Treatments
5.56
article

Autoimmune Encephalitis-like Presentation of Glioblastoma: Get to Know This Rare Occurrence

Mario Tortora, Andrea Elefante, Camilla Russo, Vincenzo D’Agostino, Eugenio Maria Covelli, Laura Gemini, A. Dal Negro, Luisa Chiapparini, Eduardo Gragnano
article en
4 citations

Abstract

<b>Background</b>: Glioblastoma (GBM) is the most common primary brain tumor in adults, with a poor prognosis and survival. Although typically presenting with focal neurological deficits, seizures, or cognitive decline, GBM can occasionally mimic autoimmune encephalitis (AE), leading to significant diagnostic delay. The overlap in clinical, radiological, and serological findings between GBM and AE underscores the need for thorough evaluation. <b>Methods</b>: We retrospectively reviewed cases of patients diagnosed between 2016 and 2023 with pathology-confirmed GBM, critically rethinking those cases initially diagnosed with AE at symptom onset. The diagnostic workup included magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, autoantibody testing, and whole-body nuclear scanning to exclude extracranial malignancies. <b>Results</b>: We found five female patients diagnosed with GBM who initially presented with signs and symptoms suggestive for AE. Initial MRI showed non-specific brain tissue alterations, without definitive tumor features. CSF analysis was largely unremarkable, though some cases exhibited positive autoantibodies. Despite therapy, clinical deterioration and follow-up MRI revealed infiltrative intra-axial lesions with contrast enhancement, leading to pathology-confirmed GBM diagnoses. All patients had poor prognoses, with a mean survival of 10 ± 4 months. <b>Conclusions</b>: GBM can mimic AE, delaying appropriate treatment. In patients with atypical MRI findings and suboptimal response to therapy, early follow-up imaging and biopsy should be considered to exclude malignancy. A multidisciplinary approach is critical for timely diagnosis and improved management.

Journal of Clinical MedicineVol. 14(11)
Santobono Children's Hospital (IT), Ospedale Sant'Anna (IT), Policlinico San Matteo Fondazione (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Naples Federico II (IT)
Good health and well-being
Openalex Percentile: Top 4%
Autoimmune Neurological Disorders and Treatments
5.56
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