ArticleSage open pediatrics
Imaging of a Rare Localization of Ewing Sarcoma in Spheno-Temporal Bone: A Case Report.
Article in Sage open pediatrics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ewing sarcoma is a malignant tumor that typically affects the appendicular skeleton; skull involvement is rare. Its clinical and radiological features are non-specific, making its diagnosis challenging. Confirmation is primarily achieved through immunohistochemistry. We report the case of a child who presented with facial swelling. MRI revealed an aggressive lesion involving the right sphenoid and temporal bones. Thoracic and abdominal CT scans showed no evidence of distant metastases. Biopsy of the lesion confirmed the diagnosis of Ewing sarcoma.
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Registered trials
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.