ArticleCureus2025
When Common Tumours Hide in Uncommon Places: Paediatric Sacral Ewing Sarcoma With Metastases.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ewing's sarcoma is a highly aggressive malignant small round blue cell tumour that typically affects the long bones and axial skeleton in children and adolescents. Sacral involvement is uncommon, often leading to diagnostic delays due to nonspecific symptoms. We report a case of a nine-year-old girl presenting with chronic back pain and weight loss, eventually found to have a large sacral mass with hepatic metastases. Imaging revealed a destructive presacral tumour with soft tissue extension, and histopathology confirmed Ewing's sarcoma with EWSR1 rearrangement. This case highlights the diagnostic challenges of rare anatomical sites, emphasises the value of multimodality imaging, and reinforces the importance of including Ewing's sarcoma in the differential for persistent paediatric back pain.
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Registered trials
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