Abstract
We describe a 12-year-old male who presented with an expressive dysphasia after completion of treatment for unifocal Ewing sarcoma. CNS vasculitis was diagnosed by MRI/MRA and cerebral angiography. Extensive rheumatologic work-up failed to identify an underlying primary process. Restaging studies showed no evidence of tumor. Complete neurologic recovery was achieved on prednisone. Four months later the patient developed overt, extensive metastases, confirmed by biopsy to represent recurrent Ewing sarcoma. Despite intensive therapy the patient succumbed 6 months later. This case demonstrates the unique finding of isolated CNS vasculitis as a presenting sign of Ewing sarcoma.
| Original language | English |
|---|---|
| Pages (from-to) | 326-328 |
| Number of pages | 3 |
| Journal | Pediatric Blood and Cancer |
| Volume | 54 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2010 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- CNS vasculitis
- Ewing sarcoma
- Paraneoplastic phenomena
Fingerprint
Dive into the research topics of 'Isolated CNS vasculitis: Unusual presentation of relapsed ewing sarcoma'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver