ArticleBrain tumor research and treatment2015
Solitary Fibrous Tumor of Central Nervous System: A Case Report.
Article in Brain tumor research and treatment, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 12 citations in OpenAlex.
- A Rare Case of Cervical Solitary Fibrous Tumor in a Pediatric Patient: Case Report and Literature Review.NeuroSci · 2025Article
- Successful multimodal management of central nervous system solitary fibrous tumor: A case report.Radiology case reports · 2025Article
- Solitary fibrous tumor of the central nervous system invading and penetrating the skull: A case report.Oncology letters · 2023Article
- A Rare Case of a Primary Leiomyoma of the Clivus in an Immunocompetent Patient and a Review of the Literature Regarding Clival Lesions.Diagnostics (Basel, Switzerland) · 2022Review
- Rare Case of Solitary Nasal Fibrous Tumor Eroding Skull-Base.Asian journal of neurosurgery · 2022Article
- Extremely rare case of intravascular solitary fibrous tumour in the inferior vena cava with review of the literature.Diagnostic pathology · 2019Review
- Solitary fibrous tumor of the pineal region with delayed ectopic intracranial metastasis: A case report and review of the literature.Medicine · 2019Article
- Spinal Intramedullary Solitary Fibrous Tumor: A Rare and Challenging Diagnosis.Cancer management and research · 2019Article
- Primary intrapulmonary solitary fibrous tumours.Oncology letters · 2018Article
- Malignant Solitary Fibrous Tumor of the Right Cerebellum: A Case Report.Case reports in neurologyArticle
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Solitary fibrous tumor (SFT) is a rare neoplasm of mesenchymal origin, especially in the central nervous system (CNS). Reported herein is a case of SFT of CNS in a 63-year-old female patient who had confused mentality, without other neurological deficit. The brain MRI showed an ovoid mass in the right frontal lobe. The tumor was surgically removed grossly and totally, and the pathologic diagnosis was SFT. At 55 months after the surgery, the tumor recurred at the primary site and at an adjacent area. A second operation was thus done, and the tumor was again surgically removed grossly and totally. The pathologic diagnosis was the same as the previous, but the Ki-67 index was elevated. Ten months later, two small recurring tumors in the right frontal skull base were found in the follow-up MRI. It was decided that radiation therapy be done, and MRI was done again 3 months later. In the follow-up MRI, the size of the recurring mass was found to have decreased, and the patient did not manifest any significant symptom. Follow-up will again be done 18 months after the second surgery.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.