Adult Primary Spinal Epidural Extraosseous Ewing’s Sarcoma: A Case Report and Review of the Literature

Author:

Bustoros Mark1ORCID,Thomas Cheddhi2,Frenster Joshua1ORCID,Modrek Aram S.1,Bayin N. Sumru1,Snuderl Matija234,Rosen Gerald35ORCID,Schiff Peter B.36,Placantonakis Dimitris G.1347ORCID

Affiliation:

1. Department of Neurosurgery, NYU School of Medicine, New York, NY 10016, USA

2. Department of Pathology, NYU School of Medicine, New York, NY 10016, USA

3. Perlmutter Cancer Center, NYU Langone Medical Center, New York, NY 10016, USA

4. Brain Tumor Center, NYU Langone Medical Center, New York, NY 10016, USA

5. Department of Medicine, NYU School of Medicine, New York, NY 10016, USA

6. Department of Radiation Oncology, NYU School of Medicine, New York, NY 10016, USA

7. Kimmel Center for Stem Cell Biology, NYU School of Medicine, New York, NY 10016, USA

Abstract

Background. Extraosseous Ewing’s sarcoma in the spinal epidural space is a rare malignancy, especially in adults.Case Presentation. A 40-year-old male presented with back pain and urinary hesitancy. MRI revealed a thoracic extradural mass with no osseous involvement. He underwent surgery for gross total resection of the mass, which was diagnosed as Ewing’s sarcoma. He was subsequently treated with chemoradiotherapy. He remains disease-free 1 year after surgery. Review of the literature indicated only 45 previously reported cases of spinal epidural extraosseous Ewing’s sarcoma in adults.Conclusions. Extraosseous Ewing’s sarcoma in the spinal epidural space is a rare clinical entity that should be included in the differential for spinal epidural masses. Its treatment is multidisciplinary but frequently requires surgical intervention due to compressive neurologic symptoms. Gross total resection appears to correlate with improved outcomes.

Publisher

Hindawi Limited

Subject

General Medicine

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