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Metastatic extraneural glioblastoma diagnosed with molecular testing.
Majd, Nazanin K; Vo, Henry Hiep; Moran, Cesar A; Weathers, Shiao-Pei; Song, I-Wen; Williford, Garret L; Rodon, Jordi; Fu, Siqing; Tsimberidou, Apostolia-Maria.
Afiliação
  • Majd NK; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Vo HH; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Moran CA; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
  • Weathers SP; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Song IW; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Williford GL; Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Rodon J; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Fu S; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
  • Tsimberidou AM; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Oncologist ; 2024 Jun 05.
Article em En | MEDLINE | ID: mdl-38837109
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article