Púrpura de Henoch-Schönlein: recorrência e cronicidade
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0021-75572007000200013 http://repositorio.unifesp.br/handle/11600/3623 |
Resumo: | OBJECTIVES: To describe a group of patients treated at our service for Henoch-Schönlein purpura, with emphasis on recurrent and chronic cases, and to compare clinical and demographic characteristics of patients with monocyclic and recurrent disease. METHODS: Data on 67 patients who had been treated since disease onset were analyzed. Twelve patients were excluded because they failed to return for follow-up consultations after less than 3 months, leaving a total of 55 children in the study sample. Recurrence was defined as the presence of a fresh episode after a period of at least 3 months without symptoms, and cases were defined as chronic when cutaneous, abdominal and renal manifestations persisted for a period of 12 months or more. RESULTS: Recurrence was observed in 8/55 patients (14.4%) and four cases were chronic (7.2%). In 29/55 patients (52.7%), infection was identified as the trigger factor. A monocyclic clinical course was observed in 43 patients (26 of whom were girls, with a mean age of 5.4 years). Gastrointestinal and renal involvement was observed in 55.8 and 20.9% of patients, respectively. Among the 12 patients with recurrent or chronic Henoch-Schönlein purpura, three had arthritis, four exhibited signs and symptoms of abdominal involvement and seven of kidney disease: microscopic hematuria in five, macroscopic hematuria in one and hematuria with proteinuria in one other. Late onset was the only variable related to recurrence (p < 0.05). CONCLUSIONS: As is observed in medical literature, monocyclic cases are more common among children with early onset disease. Patients with Henoch-Schönlein purpura should be followed over the long term, since recurrent and chronic cases account for more than 20% of the total. |
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Púrpura de Henoch-Schönlein: recorrência e cronicidadeHenoch-Schönlein purpura: recurrence and chronicityHenoch-Schönlein purpurapurpuranephritisvasculitisPúrpura de Henoch-SchönleinpúrpuranefritevasculiteOBJECTIVES: To describe a group of patients treated at our service for Henoch-Schönlein purpura, with emphasis on recurrent and chronic cases, and to compare clinical and demographic characteristics of patients with monocyclic and recurrent disease. METHODS: Data on 67 patients who had been treated since disease onset were analyzed. Twelve patients were excluded because they failed to return for follow-up consultations after less than 3 months, leaving a total of 55 children in the study sample. Recurrence was defined as the presence of a fresh episode after a period of at least 3 months without symptoms, and cases were defined as chronic when cutaneous, abdominal and renal manifestations persisted for a period of 12 months or more. RESULTS: Recurrence was observed in 8/55 patients (14.4%) and four cases were chronic (7.2%). In 29/55 patients (52.7%), infection was identified as the trigger factor. A monocyclic clinical course was observed in 43 patients (26 of whom were girls, with a mean age of 5.4 years). Gastrointestinal and renal involvement was observed in 55.8 and 20.9% of patients, respectively. Among the 12 patients with recurrent or chronic Henoch-Schönlein purpura, three had arthritis, four exhibited signs and symptoms of abdominal involvement and seven of kidney disease: microscopic hematuria in five, macroscopic hematuria in one and hematuria with proteinuria in one other. Late onset was the only variable related to recurrence (p < 0.05). CONCLUSIONS: As is observed in medical literature, monocyclic cases are more common among children with early onset disease. Patients with Henoch-Schönlein purpura should be followed over the long term, since recurrent and chronic cases account for more than 20% of the total.OBJETIVOS: Descrever um grupo de pacientes com púrpura de Henoch-Schönlein seguido em nosso serviço, com ênfase nos casos recorrentes e crônicos, e comparar pacientes com doença monocíclica ou recorrente segundo características clínicas e demográficas. MÉTODOS: Foram avaliados dados de 67 pacientes atendidos desde o início da doença. Doze pacientes foram excluídos, pois abandonaram o seguimento antes de 3 meses de acompanhamento, sendo incluídas 55 crianças no estudo. Recorrência foi definida pela presença de novo quadro após um período de 3 meses sem sintomas, e cronicidade como persistência de manifestações cutâneas, abdominais e renais por um período ≥ 12 meses. RESULTADOS: Foi observada recorrência em 8/55 pacientes (14,4 %) e cronicidade em quatro (7,2%). Em 29/55 pacientes (52,7%), foi constatada infecção como fator desencadeante. Curso monocíclico esteve presente em 43 pacientes (26 meninas, média de idade de 5,4 anos). Acometimento gastrointestinal e renal foi observado em 55,8 e 20,9% dos pacientes, respectivamente. Dentre os 12 pacientes com púrpura de Henoch-Schönlein recorrente ou crônica, três apresentaram artrite, quatro tiveram sinais e sintomas de comprometimento abdominal e sete de doença renal: hematúria microscópica em cinco, hematúria macroscópica em um e hematúria com proteinúria em um paciente. Idade de início tardia foi a única variável relacionada com a presença de recorrência (p < 0,05). CONCLUSÕES: Como observado na literatura médica, o curso monocíclico é mais freqüente nas crianças com início da doença em idade mais precoce. Pacientes com púrpura de Henoch-Schönlein devem ser seguidos a longo prazo, uma vez que recorrências e/ou cronicidade são observadas em mais de 20% dos casos.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de PediatriaUNIFESP-EPM Departamento de PediatriaUNIFESP, EPM, Depto. de PediatriaUNIFESP, EPM Depto. de PediatriaSciELOSociedade Brasileira de PediatriaUniversidade Federal de São Paulo (UNIFESP)Alfredo, Camila S. [UNIFESP]Nunes, Nicole Acacia Cabral [UNIFESP]Len, Claudio Arnaldo [UNIFESP]Barbosa, Cassia Maria Passarelli Lupoli [UNIFESP]Terreri, Maria Teresa Ramos Ascensão [UNIFESP]Hilário, Maria Odete Esteves [UNIFESP]2015-06-14T13:36:49Z2015-06-14T13:36:49Z2007-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion177-180application/pdfhttp://dx.doi.org/10.1590/S0021-75572007000200013Jornal de Pediatria. Sociedade Brasileira de Pediatria, v. 83, n. 2, p. 177-180, 2007.10.1590/S0021-75572007000200013S0021-75572007000200013.pdf0021-7557S0021-75572007000200013http://repositorio.unifesp.br/handle/11600/3623WOS:000254506000013porJornal de Pediatriainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-27T11:50:45Zoai:repositorio.unifesp.br/:11600/3623Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-27T11:50:45Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Púrpura de Henoch-Schönlein: recorrência e cronicidade Henoch-Schönlein purpura: recurrence and chronicity |
title |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
spellingShingle |
Púrpura de Henoch-Schönlein: recorrência e cronicidade Alfredo, Camila S. [UNIFESP] Henoch-Schönlein purpura purpura nephritis vasculitis Púrpura de Henoch-Schönlein púrpura nefrite vasculite |
title_short |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
title_full |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
title_fullStr |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
title_full_unstemmed |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
title_sort |
Púrpura de Henoch-Schönlein: recorrência e cronicidade |
author |
Alfredo, Camila S. [UNIFESP] |
author_facet |
Alfredo, Camila S. [UNIFESP] Nunes, Nicole Acacia Cabral [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Barbosa, Cassia Maria Passarelli Lupoli [UNIFESP] Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
author_role |
author |
author2 |
Nunes, Nicole Acacia Cabral [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Barbosa, Cassia Maria Passarelli Lupoli [UNIFESP] Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Alfredo, Camila S. [UNIFESP] Nunes, Nicole Acacia Cabral [UNIFESP] Len, Claudio Arnaldo [UNIFESP] Barbosa, Cassia Maria Passarelli Lupoli [UNIFESP] Terreri, Maria Teresa Ramos Ascensão [UNIFESP] Hilário, Maria Odete Esteves [UNIFESP] |
dc.subject.por.fl_str_mv |
Henoch-Schönlein purpura purpura nephritis vasculitis Púrpura de Henoch-Schönlein púrpura nefrite vasculite |
topic |
Henoch-Schönlein purpura purpura nephritis vasculitis Púrpura de Henoch-Schönlein púrpura nefrite vasculite |
description |
OBJECTIVES: To describe a group of patients treated at our service for Henoch-Schönlein purpura, with emphasis on recurrent and chronic cases, and to compare clinical and demographic characteristics of patients with monocyclic and recurrent disease. METHODS: Data on 67 patients who had been treated since disease onset were analyzed. Twelve patients were excluded because they failed to return for follow-up consultations after less than 3 months, leaving a total of 55 children in the study sample. Recurrence was defined as the presence of a fresh episode after a period of at least 3 months without symptoms, and cases were defined as chronic when cutaneous, abdominal and renal manifestations persisted for a period of 12 months or more. RESULTS: Recurrence was observed in 8/55 patients (14.4%) and four cases were chronic (7.2%). In 29/55 patients (52.7%), infection was identified as the trigger factor. A monocyclic clinical course was observed in 43 patients (26 of whom were girls, with a mean age of 5.4 years). Gastrointestinal and renal involvement was observed in 55.8 and 20.9% of patients, respectively. Among the 12 patients with recurrent or chronic Henoch-Schönlein purpura, three had arthritis, four exhibited signs and symptoms of abdominal involvement and seven of kidney disease: microscopic hematuria in five, macroscopic hematuria in one and hematuria with proteinuria in one other. Late onset was the only variable related to recurrence (p < 0.05). CONCLUSIONS: As is observed in medical literature, monocyclic cases are more common among children with early onset disease. Patients with Henoch-Schönlein purpura should be followed over the long term, since recurrent and chronic cases account for more than 20% of the total. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-04-01 2015-06-14T13:36:49Z 2015-06-14T13:36:49Z |
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/S0021-75572007000200013 Jornal de Pediatria. Sociedade Brasileira de Pediatria, v. 83, n. 2, p. 177-180, 2007. 10.1590/S0021-75572007000200013 S0021-75572007000200013.pdf 0021-7557 S0021-75572007000200013 http://repositorio.unifesp.br/handle/11600/3623 WOS:000254506000013 |
url |
http://dx.doi.org/10.1590/S0021-75572007000200013 http://repositorio.unifesp.br/handle/11600/3623 |
identifier_str_mv |
Jornal de Pediatria. Sociedade Brasileira de Pediatria, v. 83, n. 2, p. 177-180, 2007. 10.1590/S0021-75572007000200013 S0021-75572007000200013.pdf 0021-7557 S0021-75572007000200013 WOS:000254506000013 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Jornal de Pediatria |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
177-180 application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Pediatria |
publisher.none.fl_str_mv |
Sociedade Brasileira de Pediatria |
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_ |
1814268395927896064 |