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Isolated CNS vasculitis: Unusual presentation of relapsed ewing sarcoma

  • Polina Stepensky
  • , Elisha Waldman
  • , Natalia Simanovsky
  • , Iris Fried
  • , Shoshana Revel-Vilk
  • , Igor B. Resnick
  • , Michael Weintraub

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

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 languageEnglish
Pages (from-to)326-328
Number of pages3
JournalPediatric Blood and Cancer
Volume54
Issue number2
DOIs
StatePublished - Feb 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CNS vasculitis
  • Ewing sarcoma
  • Paraneoplastic phenomena

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