Características clínicas das espondiloartropatias na infância: análise de 26 pacientes

Detalhes bibliográficos
Autor(a) principal: Faustino, P.c. [UNIFESP]
Data de Publicação: 2001
Outros Autores: Terreri, Maria Teresa Ramos Ascensão [UNIFESP], Andrade, C.t.f. [UNIFESP], Len, Claudio Arnaldo [UNIFESP], Hilário, Maria Odete Esteves [UNIFESP]
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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spelling 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
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