{"title":"[幼年特发性关节炎]。","authors":"Lana Tambić Bukovac, Marija Perica","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Juvenile idiopathic arthritis (JIA) is the most common rheumatic disorder in children and one of the\nmost common causes of part-time or long-term disability. The term juvenile idiopathic arthritis defines the main characteristics\nof the disease: joint inflammation of unknown origin manifested before the 16th birthday and lasting for more\nthan six weeks. JIA is very rare in infancy, with highest frequency in preschool age. It is not a single disease, but a group\nof disorders with some common features of different immunopathogenesis and with different clinical manifestations. According\nto the revised International League of Associations for Rheumatology (ILAR) criteria, JIA is classified into 8\nsubtypes, but this classification is still a “work in progress“ because with new knowledge gained in genetics and immunology,\nthe classification will obviously have to be changed and refined. New research of the disease pathogenesis is the basis\nfor the development of new and better treatments for JIA. The goal of such treatments is not just to relieve pain, but also\nto control inflammation and stop irreversible joint damage and long-term disability. Biological agents have significantly\nimproved the disease prognosis.</p>","PeriodicalId":76426,"journal":{"name":"Reumatizam","volume":"63 Suppl 1 ","pages":"53-8"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[JUVENILE IDIOPATHIC ARTHRITIS].\",\"authors\":\"Lana Tambić Bukovac, Marija Perica\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Juvenile idiopathic arthritis (JIA) is the most common rheumatic disorder in children and one of the\\nmost common causes of part-time or long-term disability. The term juvenile idiopathic arthritis defines the main characteristics\\nof the disease: joint inflammation of unknown origin manifested before the 16th birthday and lasting for more\\nthan six weeks. JIA is very rare in infancy, with highest frequency in preschool age. It is not a single disease, but a group\\nof disorders with some common features of different immunopathogenesis and with different clinical manifestations. According\\nto the revised International League of Associations for Rheumatology (ILAR) criteria, JIA is classified into 8\\nsubtypes, but this classification is still a “work in progress“ because with new knowledge gained in genetics and immunology,\\nthe classification will obviously have to be changed and refined. New research of the disease pathogenesis is the basis\\nfor the development of new and better treatments for JIA. The goal of such treatments is not just to relieve pain, but also\\nto control inflammation and stop irreversible joint damage and long-term disability. Biological agents have significantly\\nimproved the disease prognosis.</p>\",\"PeriodicalId\":76426,\"journal\":{\"name\":\"Reumatizam\",\"volume\":\"63 Suppl 1 \",\"pages\":\"53-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reumatizam\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reumatizam","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Juvenile idiopathic arthritis (JIA) is the most common rheumatic disorder in children and one of the
most common causes of part-time or long-term disability. The term juvenile idiopathic arthritis defines the main characteristics
of the disease: joint inflammation of unknown origin manifested before the 16th birthday and lasting for more
than six weeks. JIA is very rare in infancy, with highest frequency in preschool age. It is not a single disease, but a group
of disorders with some common features of different immunopathogenesis and with different clinical manifestations. According
to the revised International League of Associations for Rheumatology (ILAR) criteria, JIA is classified into 8
subtypes, but this classification is still a “work in progress“ because with new knowledge gained in genetics and immunology,
the classification will obviously have to be changed and refined. New research of the disease pathogenesis is the basis
for the development of new and better treatments for JIA. The goal of such treatments is not just to relieve pain, but also
to control inflammation and stop irreversible joint damage and long-term disability. Biological agents have significantly
improved the disease prognosis.