Molecular Characterization of a Rare Glioblastoma Case With Atypical Histopathologic Features

A 76-year-old man presented with a subtle, non-mass-like right insular and temporal opercular T2 FLAIR hyperintensity that remained stable for over 2 years before showing interval progression. Resection revealed mildly hypercellular atypical glial cells with a Ki-67 index of approximately 1% and no necrosis or microvascular proliferation. Immunohistochemistry was negative for IDH1 R132H. Next-generation sequencing identified a TERT promoter mutation, EGFR amplification, and CDKN2A deletion. Methylation profiling confirmed glioblastoma, IDH wild-type, World Health Organization grade 4. Despite lacking classic histologic features, the integrated molecular findings established the diagnosis. The patient underwent near-total resection, followed by hypofractionated radiotherapy with concurrent temozolomide, maintenance temozolomide, and tumor treating fields therapy. This case highlights the essential role of molecular diagnostics in accurately classifying diffuse gliomas with atypical histology.

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Publication Details

Journal
ONCOLOGY
Published
2025-09-04
DOI
https://doi.org/10.46883/2025.25921050
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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Molecular Characterization of a Rare Glioblastoma Case With Atypical Histopathologic Features

Anup Kasi, Tolga Tuncer, Nanuli Gvazava, Wei Zhang et al.
ONCOLOGY
Glioma Diagnosis and Treatment
article

Molecular Characterization of a Rare Glioblastoma Case With Atypical Histopathologic Features

Anup Kasi, Tolga Tuncer, Nanuli Gvazava, Wei Zhang, Uma Bhoot
article en

Abstract

A 76-year-old man presented with a subtle, non-mass-like right insular and temporal opercular T2 FLAIR hyperintensity that remained stable for over 2 years before showing interval progression. Resection revealed mildly hypercellular atypical glial cells with a Ki-67 index of approximately 1% and no necrosis or microvascular proliferation. Immunohistochemistry was negative for IDH1 R132H. Next-generation sequencing identified a TERT promoter mutation, EGFR amplification, and CDKN2A deletion. Methylation profiling confirmed glioblastoma, IDH wild-type, World Health Organization grade 4. Despite lacking classic histologic features, the integrated molecular findings established the diagnosis. The patient underwent near-total resection, followed by hypofractionated radiotherapy with concurrent temozolomide, maintenance temozolomide, and tumor treating fields therapy. This case highlights the essential role of molecular diagnostics in accurately classifying diffuse gliomas with atypical histology.

ONCOLOGYVol. 39(3908)
Openalex Percentile: Top 64%
Glioma Diagnosis and Treatment
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