ArticleTranslational cancer research2022
Extracranial metastasis of glioblastoma with genomic analysis: a case report and review of the literature.
Article in Translational cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed, 7 citations in OpenAlex.
- Metastatic glioblastoma to the lungs: a case report and literature review.CNS oncology · 2024Review
- Breaking boundaries: A rare case of glioblastoma with uncommon extraneural metastases: A case report and literature review.Brain & spine · 2024Article
- Glioblastoma: an organ-confined disease?Translational cancer research · 2022Article
- Case report: Fulminant extraneural metastasis of glioblastoma through venous sinus.Frontiers in oncology · 2022Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Glioblastoma (GBM) is the first most frequent type of primary malignant brain tumors in adults. It is basically confined to the brain, and extracranial metastases (ECM) are rare. The genomic features of GBM with ECM are not fully elucidated. Case Description: Here, we present a case of a male patient with headache and left eye vision loss for 2 months who had a left occipital lobe tumor. GBM of grade IV [isocitrate dehydrogenase 1 (IDH-1) wild type] was diagnosed based on the histological profiles of intracranial tumor according to the World Health Organization standard. ECM of GBM located in the mediastinal lymph node occurred 6 months after resection of the intracranial tumor. High throughput gene sequencing was performed using ECM lesions. Mutated genes included tumor protein 53 ( Conclusions: ECM of GBM is rare, and its prognosis is very poor. Mutated genes in ECM included
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