{"id":3989,"date":"2018-09-20T07:53:15","date_gmt":"2018-09-20T07:53:15","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2018\/09\/20\/nos-adherimos-al-dia-nacional-del-sarcoma-en-espana\/"},"modified":"2018-09-20T07:53:15","modified_gmt":"2018-09-20T07:53:15","slug":"nos-adherimos-al-dia-nacional-del-sarcoma-en-espana","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2018\/09\/20\/nos-adherimos-al-dia-nacional-del-sarcoma-en-espana\/","title":{"rendered":"Nos adherimos al D\u00eda Nacional del Sarcoma en Espa\u00f1a"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p>&nbsp;<\/p>\n<p>El 20 de septiembre se conmemora el D\u00eda Nacional del Sarcoma en Espa\u00f1a y la Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras (FEDER) se unen a la celebraci\u00f3n de este d\u00eda para mostrar su apoyo a quienes conviven con este tipo de c\u00e1ncer poco frecuente.<\/p>\n<p>Un sarcoma es un tumor maligno que surge en los huesos o en los tejidos blandos del organismo, que conforman el sistema muscoesquel\u00e9tico o los encargados de sostener diferentes \u00f3rganos, como m\u00fasculos, grasa, tendones o la pared de los vasos sangu\u00edneos.<\/p>\n<p>S\u00f3lo el 1 % de los c\u00e1nceres son sarcomas y se diagnostica un sarcoma a entre 1 y 10 personas por cada 100.000. Adem\u00e1s, la Organizaci\u00f3n Mundial de la Salud reconoce m\u00e1s de 150 subtipos de sarcomas, por lo que su diagn\u00f3stico es dificultoso.<\/p>\n<p>Desde FEDER se unen a esta jornada para dar visibilidad al sarcoma y sus implicaciones con el objetivo de caminar hacia un diagn\u00f3stico temprano y mejorar la calidad de vida de los pacientes. Una acci\u00f3n que se realiza en Espa\u00f1a de la mano del tejido asociativo.<\/p>\n<p>En este sentido, la Federaci\u00f3n ha querido poner de relieve el papel de la Asociaci\u00f3n Espa\u00f1ola de Afectados por Sarcoma (AEAS) as\u00ed como de la Fundaci\u00f3n Mari Paz Jim\u00e9nez Casado, quienes adem\u00e1s de hacer visible este d\u00eda, trabajan durante el resto del a\u00f1o apoyando a este colectivo.<\/p>\n<p><h3 style=\"font-style: normal\">Tipos de sarcoma<\/h3>\n<p style=\"font-weight: 400;font-style: normal\">El sarcoma de Ewing (un tipo de sarcoma \u00f3seo) y los tumores del estroma grastrointestinal o GIST (un tipo espec\u00edfico de sarcoma de partes blandas), son tan peculiares en todos sus aspectos que se consideran aparte.<\/p>\n<p style=\"font-weight: 400;font-style: normal\">Los sarcomas de partes blandas pueden aparecer en cualquier parte del organismo. Afectan a m\u00fasculos, grasa, nervios, vasos sangu\u00edneos y tejido conectivo. Son dif\u00edciles de diagnosticar, ya que al inicio pueden pasar desapercibidos, sin manifestarse de forma clara hasta un estado evolucionado y de pron\u00f3stico m\u00e1s comprometido. Algunas de las clases m\u00e1s frecuentes son: liposarcomas, rabdomiosarcomas, fibrosarcomas, sarcomas sinoviales, leiomiosarcomas, angiosarcomas, linfagiosarcomas&#8230;<\/p>\n<p style=\"font-weight: 400;font-style: normal\">Los sarcomas del esqueleto, nacen en el hueso. Existen tres variedades principales: osteosarcomas (derivados del tejido \u00f3seo), condrosarcomas (de los cart\u00edlagos), y fibrosarcomas (del componente fibroso de los huesos). La mayor parte ocasiona dolor desde una fase precoz de desarrollo, as\u00ed que cualquier tumoraci\u00f3n dolorosa en las proximidades de una articulaci\u00f3n, que aparezca en ni\u00f1os o adultos j\u00f3venes comporta una alta sospecha de ser un sarcoma y deber\u00eda ser estudiado.<\/p>\n<p style=\"font-weight: 400;font-style: normal\">Salvo rar\u00edsimas excepciones, no son hereditarios. Mayoritariamente, el sarcoma se desarrolla en personas sin factores de riesgo conocidos, por lo que es dif\u00edcil prevenirlos.<\/p>\n<p style=\"font-weight: 400;font-style: normal\">Todos los sarcomas se pueden curar si se los diagnostica a tiempo, siendo el m\u00e9todo curativo por excelencia la cirug\u00eda. La radioterapia y tratamiento m\u00e9dicos, como quimioterapia o tratamientos modernos de tipo molecular, se pueden emplear para facilitar la operaci\u00f3n o para disminuir las probabilidades de reca\u00edda.<\/p>\n<p style=\"font-weight: 400;font-style: normal\">Fuente:&nbsp;<a href=\"http:\/\/www.aeasarcomas.org\/es\/que-es-el-sarcoma-ficha\" target=\"_blank\">AEAS<\/a>.<\/p>\n<\/p>\n<p style=\"text-align: right\">\u00daltima actualizaci\u00f3n: 20\/09\/2018.<\/p>\n<p>&nbsp;<\/p>\n<p>Fuente: FEDER <a href=\"https:\/\/enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/11152-nos-adherimos-al-d%C3%ADa-nacional-del-sarcoma-en-espa%C3%B1a\" target=\"_blank\">Nos adherimos al D\u00eda Nacional del Sarcoma en Espa\u00f1a<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: &nbsp; El 20 de septiembre se conmemora el D\u00eda Nacional del Sarcoma en Espa\u00f1a y la Federaci\u00f3n Espa\u00f1ola de Enfermedades Raras (FEDER) se unen a la celebraci\u00f3n de este d\u00eda para mostrar su apoyo a quienes conviven con este tipo de c\u00e1ncer poco [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":"","_members_access_role":[],"_members_access_error":""},"categories":[8],"tags":[36],"class_list":["post-3989","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-enfermedades-raras"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.2 - 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