Características clínicas das espondiloartropatias na infância: análise de 26 pacientes
Autor(a) principal: | |
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Data de Publicação: | 2001 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0104-42302001000300033 http://repositorio.unifesp.br/handle/11600/1231 |
Resumo: | OBJECTIVE: To evaluate retrospectively the clinical features of children and adolescents with spondiloarthropathies (Sps). METHODS: The charts of all Sps patients followed up in the outpatient Pediatric Rheumatology unit of UNIFESP-EPM, were analyzed from June 1982 to April 2000. The following demographic data were evaluated: age of onset, disease duration, clinical features, laboratory data, radiological findings, treatment and outcome. RESULTS: 10 out of 26 patients (38.4%) presented SEA, 1 patient (3.8%) undifferentiated spondiloarthrophaty, 10 (38.4%) JAS, 2 (7.7%) arthropathy related to inflammatory bowel disease, 2 (7.7%) Reiter's syndrome and 1 (3.8%) psoriatic arthritis. The average age at disease onset was 9.2 years (1 to 15 years). The patients with Reiter's syndrome presented lower age at onset (average age 6.5 years). Twenty-five out of 26 were males and 15 out of 26 were caucasians. Most patients presented peripheral arthritis in lower limbs (96.1%), enthesitis (61.5%) and positive HLA-B27 (14/23 -- 60.9%). Ten patients (38.4%) presented axial involvement. Fifteen patients had JRA or RF as diagnosis in the beginning of the disease. CONCLUSION: Although less frequent than JRA, the spondiloarthropathies must be considered in the differential diagnosis of children and adolescents, mainly among male patients with chronic arthritis. |
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Características clínicas das espondiloartropatias na infância: análise de 26 pacientesClinical and epidemiologycal features of spondyloarthropaties in childhood: analysis of 26 patientsSpondyloarthropathiesAnkylosing spondylitisSacroiliitisEnthesopathyHla-b27ChildrenAdolescentsEspondiloartropatiaEspondilite anquilosanteSacroileíteEntesopatiaHLA-B27CriançasAdolescentesOBJECTIVE: To evaluate retrospectively the clinical features of children and adolescents with spondiloarthropathies (Sps). METHODS: The charts of all Sps patients followed up in the outpatient Pediatric Rheumatology unit of UNIFESP-EPM, were analyzed from June 1982 to April 2000. The following demographic data were evaluated: age of onset, disease duration, clinical features, laboratory data, radiological findings, treatment and outcome. RESULTS: 10 out of 26 patients (38.4%) presented SEA, 1 patient (3.8%) undifferentiated spondiloarthrophaty, 10 (38.4%) JAS, 2 (7.7%) arthropathy related to inflammatory bowel disease, 2 (7.7%) Reiter's syndrome and 1 (3.8%) psoriatic arthritis. The average age at disease onset was 9.2 years (1 to 15 years). The patients with Reiter's syndrome presented lower age at onset (average age 6.5 years). Twenty-five out of 26 were males and 15 out of 26 were caucasians. Most patients presented peripheral arthritis in lower limbs (96.1%), enthesitis (61.5%) and positive HLA-B27 (14/23 -- 60.9%). Ten patients (38.4%) presented axial involvement. Fifteen patients had JRA or RF as diagnosis in the beginning of the disease. CONCLUSION: Although less frequent than JRA, the spondiloarthropathies must be considered in the differential diagnosis of children and adolescents, mainly among male patients with chronic arthritis.OBJETIVO: Avaliar retrospectivamente as características clínicas dos pacientes com diagnóstico de espondiloartropatia. MÉTODOS: Foram analisados os prontuários de todos os pacientes com diagnóstico de espondiloartropatia seguidos no ambulatório de reumatologia pediátrica da UNIFESP-EPM no período de junho de 1982 a abril de 2000. Foram avaliados a idade de início e tempo de evolução da doença, manifestações clínicas, dados laboratoriais, achados radiológicos, tratamento e evolução. RESULTADOS: Dos 26 pacientes estudados, 10 (38,4%) apresentavam SEA, um (3,8%) espondiloartropatia indiferenciada (EAI), 10 (38,4%) EAJ, dois (7,7%) artropatia da DIIC, dois (7,7%) síndrome de Reiter e um (3,8%) artrite psoriásica. O início da doença variou de 1 a 15 anos (média de 9,2 anos). Os pacientes com síndrome de Reiter tiveram menor idade de início (média de 6,5 anos). Houve predomínio do sexo masculino (25 pacientes) e da raça caucasóide (15 pacientes). A maioria dos pacientes apresentou artrite periférica em membros inferiores (96,1%), entesite (61,5%) e HLA B27 positivo (14/23 - 60,9%). Dez pacientes (38,4%) apresentaram comprometimento axial. Quinze pacientes receberam diagnóstico de ARJ ou FR no início do quadro. CONCLUSÃO: Embora menos freqüentes do que a ARJ, as espondiloartropatias devem ser consideradas no diagnóstico diferencial das crianças e adolescentes, principalmente do sexo masculino, com artrite crônica.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de PediatriaUNIFESP, EPM, Depto. de PediatriaSciELOAssociação Médica BrasileiraUniversidade Federal de São Paulo (UNIFESP)Faustino, P.c. [UNIFESP]Terreri, Maria Teresa Ramos Ascensão [UNIFESP]Andrade, C.t.f. [UNIFESP]Len, Claudio Arnaldo [UNIFESP]Hilário, Maria Odete Esteves [UNIFESP]2015-06-14T13:29:29Z2015-06-14T13:29:29Z2001-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion216-220application/pdfhttp://dx.doi.org/10.1590/S0104-42302001000300033Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 47, n. 3, p. 216-220, 2001.10.1590/S0104-42302001000300033S0104-42302001000300033.pdf0104-4230S0104-42302001000300033http://repositorio.unifesp.br/handle/11600/1231porRevista da Associação Médica Brasileirainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-06T03:45:21Zoai:repositorio.unifesp.br/:11600/1231Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-06T03:45:21Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes Clinical and epidemiologycal features of spondyloarthropaties in childhood: analysis of 26 patients |
title |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
spellingShingle |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes Faustino, P.c. [UNIFESP] Spondyloarthropathies Ankylosing spondylitis Sacroiliitis Enthesopathy Hla-b27 Children Adolescents Espondiloartropatia Espondilite anquilosante Sacroileíte Entesopatia HLA-B27 Crianças Adolescentes |
title_short |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
title_full |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
title_fullStr |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
title_full_unstemmed |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
title_sort |
Características clínicas das espondiloartropatias na infância: análise de 26 pacientes |
author |
Faustino, P.c. [UNIFESP] |
author_facet |
Faustino, P.c. [UNIFESP] Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Andrade, C.t.f. [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
author_role |
author |
author2 |
Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Andrade, C.t.f. [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Faustino, P.c. [UNIFESP] Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Andrade, C.t.f. [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
dc.subject.por.fl_str_mv |
Spondyloarthropathies Ankylosing spondylitis Sacroiliitis Enthesopathy Hla-b27 Children Adolescents Espondiloartropatia Espondilite anquilosante Sacroileíte Entesopatia HLA-B27 Crianças Adolescentes |
topic |
Spondyloarthropathies Ankylosing spondylitis Sacroiliitis Enthesopathy Hla-b27 Children Adolescents Espondiloartropatia Espondilite anquilosante Sacroileíte Entesopatia HLA-B27 Crianças Adolescentes |
description |
OBJECTIVE: To evaluate retrospectively the clinical features of children and adolescents with spondiloarthropathies (Sps). METHODS: The charts of all Sps patients followed up in the outpatient Pediatric Rheumatology unit of UNIFESP-EPM, were analyzed from June 1982 to April 2000. The following demographic data were evaluated: age of onset, disease duration, clinical features, laboratory data, radiological findings, treatment and outcome. RESULTS: 10 out of 26 patients (38.4%) presented SEA, 1 patient (3.8%) undifferentiated spondiloarthrophaty, 10 (38.4%) JAS, 2 (7.7%) arthropathy related to inflammatory bowel disease, 2 (7.7%) Reiter's syndrome and 1 (3.8%) psoriatic arthritis. The average age at disease onset was 9.2 years (1 to 15 years). The patients with Reiter's syndrome presented lower age at onset (average age 6.5 years). Twenty-five out of 26 were males and 15 out of 26 were caucasians. Most patients presented peripheral arthritis in lower limbs (96.1%), enthesitis (61.5%) and positive HLA-B27 (14/23 -- 60.9%). Ten patients (38.4%) presented axial involvement. Fifteen patients had JRA or RF as diagnosis in the beginning of the disease. CONCLUSION: Although less frequent than JRA, the spondiloarthropathies must be considered in the differential diagnosis of children and adolescents, mainly among male patients with chronic arthritis. |
publishDate |
2001 |
dc.date.none.fl_str_mv |
2001-09-01 2015-06-14T13:29:29Z 2015-06-14T13:29:29Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0104-42302001000300033 Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 47, n. 3, p. 216-220, 2001. 10.1590/S0104-42302001000300033 S0104-42302001000300033.pdf 0104-4230 S0104-42302001000300033 http://repositorio.unifesp.br/handle/11600/1231 |
url |
http://dx.doi.org/10.1590/S0104-42302001000300033 http://repositorio.unifesp.br/handle/11600/1231 |
identifier_str_mv |
Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 47, n. 3, p. 216-220, 2001. 10.1590/S0104-42302001000300033 S0104-42302001000300033.pdf 0104-4230 S0104-42302001000300033 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Revista da Associação Médica Brasileira |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
216-220 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Médica Brasileira |
publisher.none.fl_str_mv |
Associação Médica Brasileira |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268267662934016 |