PReS-FINAL-2087: Diagnosis of arthritis: history or laboratory?
نویسندگان
چکیده
Results Median age was 10 years (range 1-17). Diagnoses of the patients were Juvenile Idiopathic Arthritis (JIA) (35.7), reactive arthritis (15%), Familial Mediterranean Fever (FMF) (12.7%), connective tissue disorder/vasculitis (11.5%) and septic arthritis (3.8%). The remaining of patients (15.9%) was classified as arthritis of unknown etiology. Of all patients 51% had monoarticular, 38% had oligoarticular and 11% had polyarticular involvement. 41% of JIA patients had monoarthritis, 42% of them had oligoarthritis. Polyarthritis was detected in 16% of JIA cases. 75% of FMF patients had monoarticular arthritis. Sacroiliac tenderness was detected in 33 patients (25.2%). Seventeen of these patients were diagnosed as JIA. Uveitis was defined in 9% of patients. Diagnoses of patients with uveitis were JIA (71%) and connective tissue disorder/vasculitis (29%). Ophthalmological examination was normal in other disease groups (p < 0.05). Patients with uveitis had mostly monoarticular arthritis (50%). HLA B27 was positive in 6 patients (4%). Sacroileitis was determined in 66% of those patients. ANA was positive in 25% of patients and only 43.9% of patients with JIA had positive test for ANA. There was no significant difference in levels of acute phase reactants in different disease groups.
منابع مشابه
PReS-FINAL-2214: Validation of new pediatric criteria in diagnosis of Familial Mediterranean Fever in children
Methods Patient group was composed of 135 FMF patients. 165 patients who were admitted to our outpatient clinic with FMF like symptoms were reviewed as a control group. Demographic findings and laboratory examination of both groups were reviewed retrospectively. According to the new criteria, the diagnosis of FMF was established by the presence of two or more of five criteria (fever, abdominal ...
متن کاملPReS-FINAL-2105: Can routine clinical and laboratory data predict JIA diagnosis and disease course in acute arthritis?
Introduction The assessment of a child with acute join pain and swelling needs to differentiate between various conditions. JIA is the most common form of childhood arthritis and one of the most common chronic childhood illnesses. JIA subtypes demonstrate unique clinical presentations and clinical courses. The pain and functional disability associated with JIA cause significant burden for patie...
متن کاملPReS-FINAL-2273: Clinical and laboratory characteristics of patients with fever of unknown origin in two Colombian pediatric rheumatology centers from 2010 to 2013
Methods We included patients from a prospective diagnostic test trial called: levels of total and glycosilated ferritin in children with systemic onset juvenile idiopathic arthritis (SoJIA) and children with other causes of FUO. Patients had been referred with the diagnosis of FUO, defined as: temperature of >38.3°C at least twice per week during two or more weeks and without a clear diagnosis ...
متن کاملPReS-FINAL-2236: Continuous autoinflammatory syndromes: a single-center experience in Argentina
Methods Ad-hoc data bases from our autoinflammatory syndromes clinic were reviewed. Patients attended this clinic between May 2009 and May 2013. Demographic, clinical, laboratory and genetic data were retrieved. Autoinflammatory syndrome was defined as the presence of a chronic, systemic disease with no evidence of malignancy, infection or autoimmunity. Patients with a continuous disease course...
متن کاملPReS-FINAL-2017: Systemic onset juvenile idiopathic arthritis (SOJIA)-a 5-year survey in a pediatric rheumatology department
Introduction Systemic onset Juvenile Idiopathic Arthritis (SoJIA) is rare pediatric disease, it accounts for 10% of children with Juvenile Idiopathic Arthritis. The onset of disese can be vary nonspecific and may suggest bacterial or viral infection, malignancy or other rheumatic disease. It is highly characterised by its extra-articular systemic illness features and, in some ways, it resembles...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 11 شماره
صفحات -
تاریخ انتشار 2013