ArticleOcular oncology and pathology2017
Recurrent Orbital Solitary Fibrous Tumor in a 12-Year-Old.
Article in Ocular oncology and pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 16 citations in OpenAlex.
- Article
- Pediatric orbital solitary fibrous tumor/hemangiopericytoma presenting with isolated eyelid edema: a case report.Frontiers in pediatrics · 2026Article
- Review
- A giant orbital solitary fibrous tumor treated by surgical excision: a case report and literature review.Diagnostic pathology · 2023Review
- Clinical characteristics and prognosis of orbital solitary fibrous tumor in patients from a Chinese tertiary eye hospital.World journal of clinical cases · 2022Article
- An 8-year-old with a unilateral droopy eyelid.Digital journal of ophthalmology : DJO · 2022Article
- Orbit Solitary Fibrous Tumor: A Proposed Risk Prediction Model Based on a Case Series and Comprehensive Literature Review.Head and neck pathology · 2021Review
- Orbital solitary fibrous tumor: a clinicopathologic study from a Chinese tertiary hospital with a literature review.Cancer management and research · 2018Article
- A Solitary Fibrous Tumor of the Eyelid.Pakistan journal of medical sciencesArticle
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeTo report the clinical features and pathology of orbital solitary fibrous tumors and present a case of a recurrence in a 12-year-old boy.
methodsCase Report.
resultsA 12-year-old boy presented to our institution with double vision in upgaze for 6 months. Examination revealed 3 mm of left-sided proptosis, hypoglobus, and -3 impairment of supraduction. Magnetic resonance imaging of the orbits showed an avidly enhancing mass within the superolateral aspect of the orbit. Biopsy revealed a solitary fibrous tumor with STAT6 and CD34 positivity. Positron emission tomography-computed tomography was negative for metastatic disease. The tumor underwent excision. However, 4 months postoperatively, imaging revealed changes consistent with recurrence. A repeat lateral orbitotomy with orbital rim marginotomy was performed with complete gross excision of the tumor. The patient remains tumor-free 22 months after reoperation.
conclusionOrbital solitary fibrous tumor rarely occurs in the pediatric population. Despite initial complete gross tumor excision, this case represents the youngest individual with a recurrence to the authors' knowledge. This case of rapid recurrence may have been due to tumor seeding at the time of initial biopsy or other factors. This case increases the known spectrum of orbital solitary fibrous tumors.
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