Resumen
Cutaneous Ewing sarcoma is a rare variant that has been poorly characterized and has no standard therapy. We report 2 patients with cutaneous Ewing sarcoma and review 76 other cases reported in the literature for demographics, presentation, treatment, and outcome. Only 2 patients presented with metastatic disease, and only 8 patients developed metastatic disease. Ninety-one percent of all patients are alive despite wide variations in treatment regimens. On the basis of this summary, treatment consisting of local control with surgery and/or radiation and abbreviated chemotherapy is proposed as a treatment option for this less aggressive Ewing sarcoma.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 631-634 |
| Número de páginas | 4 |
| Publicación | Journal of Pediatric Hematology/Oncology |
| Volumen | 33 |
| N.º | 8 |
| DOI | |
| Estado | Published - dic 2011 |
| Publicado de forma externa | Sí |
Huella
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