Metastatic extraneural glioblastoma diagnosed with molecular testing

Author:

Majd Nazanin K1ORCID,Vo Henry Hiep2ORCID,Moran Cesar A3,Weathers Shiao-Pei1ORCID,Song I-Wen2ORCID,Williford Garret L1ORCID,Rodon Jordi2ORCID,Fu Siqing2ORCID,Tsimberidou Apostolia-Maria2ORCID

Affiliation:

1. Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center , Houston, TX , United States

2. Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center , Houston, TX , United States

3. Department of Pathology, The University of Texas MD Anderson Cancer Center , Houston, TX 77030 , United States

Abstract

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.

Funder

National Institutes of Health

University of Texas MD Anderson Cancer Center

Publisher

Oxford University Press (OUP)

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