{"id":225543,"date":"2026-09-02T22:10:08","date_gmt":"2026-09-03T02:10:08","guid":{"rendered":"https:\/\/fightcolorectalcancer.org\/guia-clinica-de-la-acg-diagnostico-y-tratamiento-de-los-sindromes-de-poliposis-colorrectal-adenomatosa\/"},"modified":"2026-09-21T11:59:41","modified_gmt":"2026-09-21T15:59:41","slug":"guia-clinica-de-la-acg-diagnostico-y-tratamiento-de-los-sindromes-de-poliposis-colorrectal-adenomatosa","status":"publish","type":"post","link":"https:\/\/fightcolorectalcancer.org\/es\/guia-clinica-de-la-acg-diagnostico-y-tratamiento-de-los-sindromes-de-poliposis-colorrectal-adenomatosa\/","title":{"rendered":"Gu\u00eda cl\u00ednica de la ACG: Diagn\u00f3stico y tratamiento de los s\u00edndromes de poliposis colorrectal adenomatosa"},"content":{"rendered":"<div>\n<p>Am J Gastroenterol. 1 de septiembre de 2026; 121(9):2086-2120. doi: 10.14309\/ajg.0000000000004105.<\/p>\n<p><b>RESUMEN<\/b><\/p>\n<p>Los s\u00edndromes de poliposis colorrectal adenomatosa hereditaria son s\u00edndromes sist\u00e9micos e incurables que predisponen al riesgo de c\u00e1ncer y que conllevan una morbilidad y mortalidad considerables. Se diferencian en su modo de herencia, la edad de aparici\u00f3n de la enfermedad, la expresi\u00f3n fenot\u00edpica y el riesgo de c\u00e1ncer. Los riesgos de c\u00e1ncer m\u00e1s comunes afectan al tracto gastrointestinal, incluyendo el colon, el recto, el duodeno, la ampolla y el est\u00f3mago. Identificar estos s\u00edndromes mediante la evaluaci\u00f3n de riesgos basada en los antecedentes personales y familiares y las pruebas gen\u00e9ticas germinales, junto con un tratamiento quir\u00fargico y endosc\u00f3pico oportuno, puede reducir la incidencia y la mortalidad por c\u00e1ncer. Estas gu\u00edas utilizan la metodolog\u00eda de \u00abClasificaci\u00f3n de Recomendaciones, Evaluaci\u00f3n, Desarrollo y Valoraci\u00f3n para ofrecer orientaci\u00f3n cl\u00ednica sobre la selecci\u00f3n de personas que deber\u00edan someterse a una evaluaci\u00f3n de riesgo de s\u00edndrome de poliposis colorrectal adenomatosa hereditaria, la modalidad y el momento adecuado para las pruebas gen\u00e9ticas germinales, la reducci\u00f3n del riesgo de c\u00e1ncer mediante intervenciones endosc\u00f3picas y quir\u00fargicas, y el papel de la quimioprevenci\u00f3n. Este documento repasa el enfoque de las pruebas gen\u00e9ticas en pacientes con poliposis colorrectal fenot\u00edpica y el impacto del diagn\u00f3stico presintom\u00e1tico en familias con una variante pat\u00f3gena germinal familiar conocida o con caracter\u00edsticas cl\u00ednicas que sugieran un s\u00edndrome de poliposis adenomatosa hereditaria. Se ofrecen estrategias de tratamiento para pacientes basadas en los resultados de las pruebas gen\u00e9ticas o sin ellas. Tambi\u00e9n repasamos las manifestaciones fenot\u00edpicas benignas y malignas, tanto colorrectales como extracol\u00f3nicas, de los s\u00edndromes hereditarios conocidos, centr\u00e1ndonos en los dos s\u00edndromes de poliposis colorrectal hereditaria m\u00e1s comunes: la poliposis adenomatosa familiar y la poliposis asociada a MUTYH. El documento concluye con recomendaciones sobre estrategias para reducir el riesgo de poliposis y c\u00e1ncer, y destaca las novedades en el tratamiento desde que se public\u00f3 la gu\u00eda anterior.        <\/p>\n<p>PMID:<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/42683623\/?utm_source=SimplePie&#038;utm_medium=rss&#038;utm_campaign=pubmed-2&#038;utm_content=1zCzv8cgXYLTFpYKqcnmEQSRKKzgHYU2epGXR7qqB04ouFsEtP&#038;fc=20260305170338&#038;ff=20260902221008&#038;v=2.20.1\">42683623<\/a> | DOI:<a href=\"https:\/\/doi.org\/10.14309\/ajg.0000000000004105\">10.14309\/ajg.0000000000004105<\/a><\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>Am J Gastroenterol. 1 de septiembre de 2026; 121(9):2086-2120. doi: 10.14309\/ajg.0000000000004105. RESUMEN Los s\u00edndromes de poliposis colorrectal adenomatosa hereditaria son s\u00edndromes sist\u00e9micos e incurables que predisponen al riesgo de c\u00e1ncer y que conllevan una morbilidad y mortalidad considerables. Se diferencian en su modo de herencia, la edad de aparici\u00f3n de la enfermedad, la expresi\u00f3n fenot\u00edpica [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[633],"tags":[],"class_list":["post-225543","post","type-post","status-publish","format-standard","hentry","category-investiga"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Gu\u00eda cl\u00ednica de la ACG: Diagn\u00f3stico y tratamiento de los s\u00edndromes de poliposis colorrectal adenomatosa - Fight Colorectal Cancer<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/fightcolorectalcancer.org\/es\/guia-clinica-de-la-acg-diagnostico-y-tratamiento-de-los-sindromes-de-poliposis-colorrectal-adenomatosa\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Gu\u00eda cl\u00ednica de la ACG: Diagn\u00f3stico y tratamiento de los s\u00edndromes de poliposis colorrectal adenomatosa - Fight Colorectal Cancer\" \/>\n<meta property=\"og:description\" content=\"Am J Gastroenterol. 1 de septiembre de 2026; 121(9):2086-2120. doi: 10.14309\/ajg.0000000000004105. 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