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Extraskeletal Ewing Sarcoma: A Case Report.
Denis, Ryan; Felix, Martin; Mejia, Daniela; Hobbs, Mikayla; Alvarez, Paul; Casadesus, Damian.
Afiliación
  • Denis R; Internal Medicine, St. George's University School of Medicine, St. George, GRD.
  • Felix M; Internal Medicine, St. George's University School of Medicine, St. George, GRD.
  • Mejia D; Internal Medicine, St. George's University School of Medicine, St. George, GRD.
  • Hobbs M; Internal Medicine, St. George's University School of Medicine, St. George, GRD.
  • Alvarez P; Internal Medicine, St. George's University School of Medicine, St. George, GRD.
  • Casadesus D; Internal Medicine, Jackson Memorial Hospital, Miami, USA.
Cureus ; 16(2): e55077, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38550497
ABSTRACT
Ewing sarcoma is one of the most common primary bone tumors arising from neuroectodermal cells mainly presenting in the younger population. Instances of this highly malignant tumor manifesting outside of the bone and outside of the typical age range create an unfamiliar clinical scenario. In this report, we present a rare extraskeletal Ewing sarcoma in a 42-year-old woman with a subcutaneous soft tissue mass in the posterior chest displaying a positive EWSR1 gene rearrangement via fluorescence in situ hybridization. The patient is currently on a chemotherapy regimen showing favorable response to the tumor size despite additional complications. This overall presentation of Ewing sarcoma allows further understanding of the malignancy and fosters better care for future cases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cureus Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cureus Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos