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Primary intradural/extradural Ewing’s sarcoma of the sacral spine: A case report and literature review

BACKGROUND: Ewing’s sarcoma (ES) is a malignant mesenchymal tumor, most often found in the long bones, and usually affecting children and adolescents in the second decade of life. ES of the spine is a clinical rarity. CASE DESCRIPTION: A 45-year-old male presented with a 3-month history of lower bac...

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Detalles Bibliográficos
Autores principales: Murray, Daniel B, Horan, Jack, Beausang, Alan, Husien, Mohammed Ben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827301/
https://www.ncbi.nlm.nih.gov/pubmed/33500832
http://dx.doi.org/10.25259/SNI_766_2020
Descripción
Sumario:BACKGROUND: Ewing’s sarcoma (ES) is a malignant mesenchymal tumor, most often found in the long bones, and usually affecting children and adolescents in the second decade of life. ES of the spine is a clinical rarity. CASE DESCRIPTION: A 45-year-old male presented with a 3-month history of lower back pain which acutely worsened in conjunction with urinary retention. The magnetic resonance imaging revealed a mass extending from L5 to S2 with additional extension through the left S2-3 neural foramen. The metastatic workup was negative. At surgery, the lesion was both intradural and extradural. Following complete surgical resection, the patient was later treated with radiation and chemotherapy. CONCLUSION: Here, we report an adult male who acutely presented with low back pain attributable to primary intradural/extradural sacral ES.