Résumé
Nous rapportons un cas de sarcome d’Ewing des parties molles, pathologie rare de l’adulte jeune. II n’existe pas de signes cliniques ou radiologiques spécifiques, TDM ou IRM et le diagnostic est anatomopathologique. Néanmoins, c’est un diagnostic à évoquer de principe devant toute tumeur primitive des parties molles.
Abstract
A case of intraosseous Ewing sarcoma is reported. This pathology of the young adult is very rare, clinical or imaging (CT or MRI) findings are non-specific and diagnosis is based on histology. Nonethless, this diagnosis should be considered in all patients with primary soft tissue tumors.
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El Andaloussi, Y., Hachimi, K., Fnini, S. et al. Sarcome d’Ewing des parties molles. À propos d’un cas et revue de la littérature. Oncologie 9, 310–312 (2007). https://doi.org/10.1007/s10269-007-0627-z
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DOI: https://doi.org/10.1007/s10269-007-0627-z