AI Article Synopsis

  • Glioblastoma is the most common and aggressive brain tumor in adults, with a survival rate of less than 2 years and very low rates of extraneural metastasis.
  • A unique case is presented where extensive metastasis occurred outside the brain, diagnosed through next-generation sequencing (NGS) rather than traditional histology.
  • The molecular analysis revealed key alterations shared between the original tumor and the metastatic sites, highlighting the critical role of NGS in identifying and understanding rare cases of extraneural glioblastoma metastasis.

Article Abstract

Glioblastoma, the most common malignant brain tumor in adults, is associated with a median overall survival duration of less than 2 years. Extraneural metastases occur in less than 1% of all patients with glioblastoma. The mechanism of extraneural metastasis is unclear. We present a case of extensive extraneural, extraosseous, epidural, and soft-tissue metastasis of glioblastoma. The diagnosis of metastatic glioblastoma was made only after next-generation sequencing (NGS) of the metastatic paraspinal lesions was completed. The CDK4, pTERT, PTEN, and TP53 molecular alterations seen in the initial intracranial glioblastoma were found in the paraspinal tumor, along with the addition of MYC, which is implicated in angiogenesis and epidermal-to-mesenchymal transition. Immunohistochemical stains showed that neoplastic cells were negative for GFAP. In conclusion, this case raises awareness about the role of NGS in the diagnosis of extraneural glioblastoma. This diagnosis was not possible with histology alone and only became evident after molecular profiling of the metastatic lesions and its comparison to the original tumor.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11379637PMC
http://dx.doi.org/10.1093/oncolo/oyae115DOI Listing

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