Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

País/Região como assunto
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Curr Rheumatol Rev ; 14(2): 163-171, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29308742

RESUMO

BACKGROUND: Juvenile Idiopathic Arthritis (JIA) is the most common inflammatory joint disease in children. JIA and autoimmune inflammatory Gastrointestinal (GI) diseases share common etiologic mechanisms, including genetic predisposition and environmental influences. OBJECTIVE: To Investigate association between gastrointestinal, rheumatologic clinical variables and the presence of autoantibodies in patients with JIA in treatment. METHODOLOGY: In a cross-sectional study of patients with JIA according to diagnostic criteria and the ILAR classification. GI symptoms and autoantibody expression were evaluated with respect to their association with JIA clinical variables. Anti-Saccharomyces Cerevisiae IgG/IgA (ASCA), 6 antigen associated with anti polymorphonuclear neutrophil (ANCA), anti Transglutaminase (tTG) IgG/IgA, anti deaminated gliadin peptide (DGP) IgG/IgA autoantibodies, ANAS and IgA were measured in all patients. The association between clinical variables and auto-antibodies were evaluated using the Fisher test with significant value of p <0.05. The study was approved by the ethics committee of the all institutions. RESULTS: Samples were collected from ninety-seven patients, 63% of whom were female. The average age was 14 years. The JIA subtype associated with the most common GI symptoms was enthesitis- related arthritis. Of these patients, 44.3% and 14% reported abdominal pain and diarrhea, respectively. Anti-DPG and anti-tTG antibodies were found in 9.28% and 7.22%, respectively and 11.34% were positive for p-ANCA, and 2% were positive for ASCA. CONCLUSION: GI symptoms and autoantibodies associated with inflammation of the GI mucosa were detected in JIA patients but were not associated with autoantibodies or clinical variables. However, it is the monitoring of these patients diagnosis is important.


Assuntos
Dor Abdominal/epidemiologia , Artrite Juvenil/imunologia , Autoanticorpos/sangue , Diarreia/epidemiologia , Adolescente , Artrite Juvenil/sangue , Artrite Juvenil/complicações , Autoantígenos/imunologia , Criança , Pré-Escolar , Colômbia , Estudos Transversais , Feminino , Humanos , Lactente , Masculino
2.
Medicina (Bogotá) ; 40(1(120)): 160-160, Ene-Mar, 2018.
Artigo em Espanhol | LILACS | ID: biblio-910269

RESUMO

Introducción y objetivo: La uveitis en la artritis idiopática juvenil (AIJ) es causa de importan-te morbilidad. La cronicidad de inflamación intraocular determina severidad de complicacio-nes y secuelas. El objetivo del estudio es evaluar la extensión, tratamiento y complicaciones de la uveítis crónica en pacientes con AIJ. Métodos: Estudio descriptivo, retrospectivo. Se in-cluyeron pacientes con seguimiento mínimo de 24 meses por oftalmología y reumatología. Se analizaron variables dermográficas, clínicas, complicaciones y tratamiento. La uveitis se eva-luó según clasificación SUN (standardization of uveítis nomenclature).


Assuntos
Uveíte , Artrite Juvenil , Pediatria
3.
Medicina (Bogotá) ; 40(1(120)): 157-157, Ene-Mar, 2018.
Artigo em Espanhol | LILACS | ID: biblio-910266

RESUMO

ntroducción y objetivo: Las tiroidopatias autoimmunes juveniles (TAIJ) son las enfermeda-des órgano específicas más comunes y con frecuencia hacen parte de la enfermedad autoin-mune múltiple (EAIM). El objetivo del estudio es determinar el tipo y frecuencia de TAIJ en pacientes con poliautoinmunidad. Métodos: En un registro de pacientes juveniles que du-rante el seguimiento en 13 centros de reumatología pediátrica, han asociado enfermedades autoinmunes (EAI), se identificaron pacientes con TAIJ.


Assuntos
Doenças Autoimunes , Pediatria
4.
Medicina (Bogotá) ; 40(1(120)): 158-158, Ene-Mar, 2018.
Artigo em Espanhol | LILACS | ID: biblio-910267

RESUMO

Introduccion: El síndrome antifosfolipídico (SAF) condiciona hipercoagulabilidad y pue-de provocar manifestaciones no trombóticas. Se asocia o no a otra enfermedad autoinmune (EAI). En el presente estudio se exploraron diferencias entre géneros en cohortes de pacientes juveniles con SAF. Métodos: Estudio retrospectivo descriptivo. Se revisaron historias clínicas de pacientes con SAF seguidos en 13 centros de reumatología pediátrica en Colombia y en Hospital San Joan (Barcelona, España). Se determinaron variables demográficas y frecuencia de manifestaciones clínicas y resultados serológicos.


Assuntos
Anticorpos Anticardiolipina , Síndrome Antifosfolipídica , Pediatria
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA