{"id":2390,"date":"2012-12-12T14:31:38","date_gmt":"2012-12-12T14:31:38","guid":{"rendered":"https:\/\/medicalcriteria.com\/web\/reujia\/"},"modified":"2025-05-13T20:28:17","modified_gmt":"2025-05-13T20:28:17","slug":"reujia","status":"publish","type":"post","link":"https:\/\/medicalcriteria.com\/web\/es\/reujia\/","title":{"rendered":"Criterios de Clasificaci\u00f3n ILAR para Artritis Idiop\u00e1tica Juvenil (AIJ)"},"content":{"rendered":"<div class=\"7ca9444b8380138fe077da07353677a4\" data-index=\"1\" style=\"float: none; margin:0px 0 0px 0; text-align:center;\">\n<script async src=\"https:\/\/pagead2.googlesyndication.com\/pagead\/js\/adsbygoogle.js\"><\/script>\r\n<!-- MC 2019- Horizontal -->\r\n<ins class=\"adsbygoogle\"\r\n     style=\"display:block\"\r\n     data-ad-client=\"ca-pub-0127150553352455\"\r\n     data-ad-slot=\"3806776041\"\r\n     data-ad-format=\"auto\"\r\n     data-full-width-responsive=\"true\"><\/ins>\r\n<script>\r\n     (adsbygoogle = window.adsbygoogle || []).push({});\r\n<\/script>\n<\/div>\n<p>La artritis idiop\u00e1tica juvenil (AIJ) es un grupo heterog\u00e9neo de enfermedades caracterizadas por la\u00a0causa desconocida de la\u00a0artritis con inicio antes de los 16 a\u00f1os.<br \/>\n<!--more--><br \/>\n<strong>Criterios de Clasificaci\u00f3n de la\u00a0Liga Internacional de Asociaciones de Reumatolog\u00eda (ILAR) para la Artritis Idiop\u00e1tica Juvenil (AIJ)<\/strong><br \/>\nLa AIJ se puede diagnosticar si la edad de inicio es menor de 16 a\u00f1os, la duraci\u00f3n de la enfermedad es de 6 semanas o m\u00e1s, y otras enfermedades conocidas est\u00e1n excluidas.<\/p>\n<ul>\n<li><strong>AIJ de comienzo sist\u00e9mico:<\/strong>\u00a0La artritis sist\u00e9mica se diagnostica si existe artritis en una o m\u00e1s articulaciones, con o precedida por fiebre de al menos 2 semanas duraci\u00f3n. Los signos o s\u00edntomas deben estar documentados diariamente durante al menos 3 d\u00edas y acompa\u00f1ado por 1 o m\u00e1s de los siguientes: erupci\u00f3n evanescente, linfadenopat\u00eda generalizada, hepato\/esplenomegalia, serositis. (Las exclusiones son A, B, C, y D de la lista de exclusi\u00f3n de m\u00e1s abajo)<\/li>\n<li><strong>Oligoartritis persistente o extendida:<\/strong>\u00a0Oligoartritis se diagnostica si hay artritis que afecta 1 a 4 articulaciones durante los primeros 6 meses. La oligoartritis persistente afecta hasta 4 articulaciones de todo el curso de la enfermedad, y la oligoartritis extendida afecta a m\u00e1s de 4 articulaciones despu\u00e9s de los primeros 6 meses de la enfermedad. (Las exclusiones son A, B, C, D, y E a partir de la lista de exclusi\u00f3n de m\u00e1s abajo)<\/li>\n<li><strong>Poliartritis (FR-negativo):\u00a0<\/strong>La poliartritis (FR-negativo) se diagnostica si hay\u00a0artritis con\u00a0factor reumatoide (FR)-negativo que afecta a 5 o m\u00e1s articulaciones durante los primeros 6 meses de enfermedad. (Las exclusiones son A, B, C, D, y E a partir de la lista de exclusi\u00f3n\u00a0de m\u00e1s abajo)<\/li>\n<li><strong>Poliartritis (FR-positivo):<\/strong>\u00a0La poliartritis (FR-positivo) se diagnostica si hay\u00a0artritis\u00a0FR-positivo que afecta a 5 o m\u00e1s articulaciones durante los primeros 6 meses de enfermedad. Dos o m\u00e1s pruebas de FR (tomadas al menos con 3 meses de diferencia) son positivos durante los primeros 6 meses de la enfermedad. (Las exclusiones son A, B, C, y E a partir de la lista de exclusi\u00f3n\u00a0de m\u00e1s abajo)<\/li>\n<li><strong>Artritis psori\u00e1sica:\u00a0<\/strong>La artritis psori\u00e1sica se diagnostica si hay artritis y psoriasis, o artritis y al menos 2 de los siguientes: dactilitis, piqueteado ungueal, onicolisis, y\/o antecedentes familiares de psoriasis (en un familiar de primer grado). (Las exclusiones son B, C, D, y E a partir de la lista de exclusi\u00f3n\u00a0de m\u00e1s abajo)<\/li>\n<li><strong>Artritis relacionada con Entesitis:<\/strong> La artritis relacionada con la entesitis se diagnostica si hay artritis y\/o entesitis con al menos 2 de los siguientes: presencia o historia de sensibilidad en articulaci\u00f3n sacroil\u00edaca con o sin dolor lumbosacro inflamatorio; presencia de ant\u00edgeno HLA B27; inicio de la artritis en un var\u00f3n de m\u00e1s de 6 a\u00f1os de edad; uve\u00edtis anterior aguda (sintom\u00e1tica), historia de la espondilitis anquilosante, artritis relacionada con entesitis, sacroile\u00edtis con enfermedad inflamatoria intestinal, s\u00edndrome de Reiter, o uve\u00edtis anterior aguda en un familiar de primer grado. (Las exclusiones son A, D y E de la lista de exclusi\u00f3n de m\u00e1s abajo.)<\/li>\n<li><strong>Indiferenciada:<\/strong>\u00a0La artritis indiferenciada se diagnostica si hay artritis que no cumple con los criterios de ninguna de las categor\u00edas anteriores, o que cumple los criterios para 2 o m\u00e1s de las categor\u00edas anteriores.<\/li>\n<\/ul>\n<p><strong>Exclusiones:<\/strong><br \/>\nA. Psoriasis o antecedentes de psoriasis en los pacientes o familiares de primer grado.<br \/>\nB. Varones con artritis en HLA B27 positivos comenzando a partir de los 6 a\u00f1os.<br \/>\nC. Espondilitis anquilosante, artritis relacionada con entesitis, sacroileitis con enfermedad inflamatoria intestinal, s\u00edndrome de Reiter, uve\u00edtis anterior aguda, o antecedentes de 1 de estos trastornos en familiares de primer grado.<br \/>\nD. Presencia de factor reumatoide IgM por lo menos en 2 ocasiones por lo menos con 3 meses de diferencia.<br \/>\nE. Presencia de AIJ sist\u00e9mica en los pacientes.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Bibliograf\u00eda:<\/strong><\/p>\n<ol>\n<li>Merino R, de Inocencio J, Garcia-Consuegra J. Evaluation of Revised International League of Associations for Rheumatology Classification Criteria for Juvenile Idiopathic Arthritis in Spanish Children (Edmonton 2001). J Rheumatol 2005;32:559-61. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/15742453\/\" target=\"_blank\" rel=\"noopener noreferrer\">[Medline]<\/a><\/li>\n<li>Petty RE, Southwood TR, Manners P, et al. International League of Associations for Rheumatology. International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001. J Rheumatol. 2004;31:390-392. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/14760812\/\" target=\"_blank\" rel=\"noopener noreferrer\">[Medline]<\/a><\/li>\n<li>Prakken B, Albani S, Martini A. Juvenile idiopathic arthritis. Lancet. 2011;377(9783):2138-2149. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/21684384\/\" target=\"_blank\" rel=\"noopener noreferrer\">[Medline]<\/a><\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<p>Creado Dic 12, 2012.<\/p>\n\n<div style=\"font-size: 0px; height: 0px; line-height: 0px; margin: 0; padding: 0; clear: both;\"><\/div>","protected":false},"excerpt":{"rendered":"<p>La artritis idiop\u00e1tica juvenil (AIJ) es un grupo heterog\u00e9neo de enfermedades caracterizadas por la\u00a0causa desconocida de la\u00a0artritis con inicio antes de los 16 a\u00f1os.<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_lmt_disableupdate":"","_lmt_disable":"","_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"categories":[45],"tags":[1069,1068,1067,166,167,16,15,65,64,1066,1065,1064,1063,1062,1070],"class_list":["post-2390","post","type-post","status-publish","format-standard","hentry","category-rheumatology","tag-arthritis","tag-artritis","tag-associations","tag-clasificacion","tag-classification","tag-criteria","tag-criterios","tag-idiopathic","tag-idiopatica","tag-ilar","tag-international","tag-juvenil","tag-juvenile","tag-league","tag-rheumatology"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - 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