Síndrome de Prune Belly

Detalhes bibliográficos
Autor(a) principal: Teixeira,Roni Leonardo
Data de Publicação: 2004
Outros Autores: Petreca,Alexandre, Garcia,Patrícia Andréa Torres
Tipo de documento: Relatório
Idioma: por
Título da fonte: Revista do Colégio Brasileiro de Cirurgiões
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-69912004000600013
Resumo: Prune Belly Syndrome is a fetal uropathy of unknown etiology with incidence of 1/35000 to 1/50000 alive been born, characterized by a classical triad: abdominal musculature congenital deficiency, bilateral criptorquidia and urinary tract malformations. The authors present a case of this rare pathology associated with a patent urachus. After complementary exams confirmed urinary tract alterations (bilateral ureterohidronefrosis and vesicoureteral reflux degree 5, besides urinary infection), the surgical approach was vesicostomy to decrease urinary infections and sepsis. Definitve surgery should be accomplished around the 12th month of life. Nowadays, the child is asymptomatic , with follow-up every two months, with return consultation bimonthly.
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spelling Síndrome de Prune BellyPrune Belly syndromeInfantnewborndiseasesCystostomyPrune Belly Syndrome is a fetal uropathy of unknown etiology with incidence of 1/35000 to 1/50000 alive been born, characterized by a classical triad: abdominal musculature congenital deficiency, bilateral criptorquidia and urinary tract malformations. The authors present a case of this rare pathology associated with a patent urachus. After complementary exams confirmed urinary tract alterations (bilateral ureterohidronefrosis and vesicoureteral reflux degree 5, besides urinary infection), the surgical approach was vesicostomy to decrease urinary infections and sepsis. Definitve surgery should be accomplished around the 12th month of life. Nowadays, the child is asymptomatic , with follow-up every two months, with return consultation bimonthly.Colégio Brasileiro de Cirurgiões2004-12-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-69912004000600013Revista do Colégio Brasileiro de Cirurgiões v.31 n.6 2004reponame:Revista do Colégio Brasileiro de Cirurgiõesinstname:Colégio Brasileiro de Cirurgiões (CBC)instacron:CBC10.1590/S0100-69912004000600013info:eu-repo/semantics/openAccessTeixeira,Roni LeonardoPetreca,AlexandreGarcia,Patrícia Andréa Torrespor2006-02-21T00:00:00Zoai:scielo:S0100-69912004000600013Revistahttp://www.scielo.br/rcbcONGhttps://old.scielo.br/oai/scielo-oai.php||revistacbc@cbc.org.br1809-45460100-6991opendoar:2006-02-21T00:00Revista do Colégio Brasileiro de Cirurgiões - Colégio Brasileiro de Cirurgiões (CBC)false
dc.title.none.fl_str_mv Síndrome de Prune Belly
title Síndrome de Prune Belly
spellingShingle Síndrome de Prune Belly
Teixeira,Roni Leonardo
Prune Belly syndrome
Infant
newborn
diseases
Cystostomy
title_short Síndrome de Prune Belly
title_full Síndrome de Prune Belly
title_fullStr Síndrome de Prune Belly
title_full_unstemmed Síndrome de Prune Belly
title_sort Síndrome de Prune Belly
author Teixeira,Roni Leonardo
author_facet Teixeira,Roni Leonardo
Petreca,Alexandre
Garcia,Patrícia Andréa Torres
author_role author
author2 Petreca,Alexandre
Garcia,Patrícia Andréa Torres
author2_role author
author
dc.contributor.author.fl_str_mv Teixeira,Roni Leonardo
Petreca,Alexandre
Garcia,Patrícia Andréa Torres
dc.subject.por.fl_str_mv Prune Belly syndrome
Infant
newborn
diseases
Cystostomy
topic Prune Belly syndrome
Infant
newborn
diseases
Cystostomy
description Prune Belly Syndrome is a fetal uropathy of unknown etiology with incidence of 1/35000 to 1/50000 alive been born, characterized by a classical triad: abdominal musculature congenital deficiency, bilateral criptorquidia and urinary tract malformations. The authors present a case of this rare pathology associated with a patent urachus. After complementary exams confirmed urinary tract alterations (bilateral ureterohidronefrosis and vesicoureteral reflux degree 5, besides urinary infection), the surgical approach was vesicostomy to decrease urinary infections and sepsis. Definitve surgery should be accomplished around the 12th month of life. Nowadays, the child is asymptomatic , with follow-up every two months, with return consultation bimonthly.
publishDate 2004
dc.date.none.fl_str_mv 2004-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv 10.1590/S0100-69912004000600013
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Colégio Brasileiro de Cirurgiões
publisher.none.fl_str_mv Colégio Brasileiro de Cirurgiões
dc.source.none.fl_str_mv Revista do Colégio Brasileiro de Cirurgiões v.31 n.6 2004
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instname:Colégio Brasileiro de Cirurgiões (CBC)
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repository.name.fl_str_mv Revista do Colégio Brasileiro de Cirurgiões - Colégio Brasileiro de Cirurgiões (CBC)
repository.mail.fl_str_mv ||revistacbc@cbc.org.br
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