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- W60932171 abstract "Resumen El rabdomiosarcoma (RMS) es un tumor maligno derivado de las celulas mesenquimales precursoras del musculo estriado. Es el tumor de tejidos blandos mas frecuente en ninos, y son la extremidad cefalica, cuello, tracto genitourinario y extremidades los sitios mas frecuentemente afectados. Los dos subtipos histologicos principales son el embrionario y el alveolar. El tratamiento dependera de la estadificacion del tumor, que incluye dentro de las modalidades terapeuticas cirugia, quimioterapia y/o irradiacion. En la actualidad, el RMS tiene una sobrevida de aproximadamente el 70%. El rapido reconocimiento y la posibilidad de un tratamiento efectivo y precoz permitira mejorar la sobrevida y evitar secuelas invalidantes (Dermatol. Argent., 2012, 18(6): 433-441). Palabras clave : rabdomiosarcoma, sarcomas de tejidos blandos, ninos. Childhood rhabdomyosarcoma Abstract Rhabdomyosarcoma is a malignant tumour that originates in the primitive mesenchymal cells, precursors of the striated skeletal muscle. It is the most common soft tissue sarcoma of childhood. The head, neck, genitourinary system and the extremities are the sites more frequently affected by this tumor. The main histological variants are the embryonal and the alveolar subtype. Treatment depends of tumor stage and includes surgery, chemotherapy and/or radiotherapy. Currently, pediatric rhabdomyosarcoma has an overall survival of 70%. Early diagnosis and treatment of this rare disorder facilitate patients long-term survival and prevent severe sequels (Dermatol. Argent., 2012, 18(6): 433-441). Keywords : rhabdomyosarcoma, soft tissue sarcoma, children." @default.
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- W60932171 date "2012-01-01" @default.
- W60932171 modified "2023-09-27" @default.
- W60932171 title "Rabdomiosarcomas en la infancia." @default.
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