{"id":15241,"date":"2014-02-19T13:45:00","date_gmt":"2014-02-19T19:45:00","guid":{"rendered":"http:\/\/www.cmeded.com\/?page_id=15241"},"modified":"2025-04-27T21:28:39","modified_gmt":"2025-04-28T02:28:39","slug":"overview","status":"publish","type":"page","link":"https:\/\/cmeded.com\/es\/childhood\/understanding-ewings-sarcoma\/overview\/","title":{"rendered":"Generalidades"},"content":{"rendered":"

\"Sarcoma<\/a>

Click Image to Enlarge.<\/p><\/div><\/div>
\n

<\/p>\n

\u00bfQu\u00e9 es el sarcoma de Ewing?<\/h4>\n

El sarcoma de Ewing es un tipo de c\u00e1ncer de hueso poco frecuente que suele aparecer en ni\u00f1os y adolescentes. Se diagnostican alrededor de 250 casos nuevos de sarcoma de Ewing en Estados Unidos por a\u00f1o. Si bien por lo general el sarcoma de Ewing tiene lugar en pacientes que tienen entre 10 y 20 a\u00f1os de edad, los beb\u00e9s y los adultos tambi\u00e9n pueden contraer la enfermedad. Se origina con mayor frecuencia en la columna vertebral, la pelvis, la pared tor\u00e1cica, las piernas y los brazos. El sarcoma de Ewing se debe a un cambio gen\u00e9tico en una c\u00e9lula donde el ADN se intercambia entre los cromosomas 11 y 22, convirti\u00e9ndola en una c\u00e9lula cancerosa. Sin embargo, se desconocen las causas de esta \"translocaci\u00f3n\" cromos\u00f3mica.<\/p>\n

<\/div>

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