Association of posterior urethral valve with congenital lobar emphysema: a case report

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dc.creatorThiago Luiz do Nascimentolazaroni
dc.creatorFabio Mendes Botelho Filho
dc.creatorMarcelo Eller Miranda
dc.creatorAtila Magalhães Victoria
dc.creatorPaulo Custódio Furtado Cruzeiro
dc.creatorClecio Piçarro Piçarro
dc.date.accessioned2023-05-12T19:48:23Z
dc.date.accessioned2025-09-08T23:25:52Z
dc.date.available2023-05-12T19:48:23Z
dc.date.issued2016
dc.format.mimetypepdf
dc.identifier.doi10.14534/PUCR.2016316895
dc.identifier.issn21482969
dc.identifier.urihttps://hdl.handle.net/1843/53219
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofPediatric Urology Case Reports
dc.rightsAcesso Aberto
dc.subjectPneumopatias
dc.subjectEnfisema
dc.subjectCriança
dc.subject.otherPosterior urethral valve
dc.subject.otherCongenital lobar emphysema;
dc.subject.otherChild
dc.titleAssociation of posterior urethral valve with congenital lobar emphysema: a case report
dc.typeArtigo de periódico
local.citation.epage88
local.citation.issue3
local.citation.spage84
local.citation.volume3
local.description.resumoPosterior Urethral Valve (PUV) is the most common cause of bladder outlet obstruction in boys, with an incidence of 1 in 5,000 to 8,000 male births. Congenital lobar emphysema (CLE) is an uncommon cause of congenital pulmonary airway malformation, with an incidence 1 per 20,000 to 30,000 deliveries. These congenital malformations have never been described together before.A boy newborn with prenatal suspicion of PUV, confirmed in first days of live presented respiratory distress that lead CLE diagnosis. Our multidisciplinary team submitted him to a twostep surgery correction successfully.
local.publisher.countryBrasil
local.publisher.departmentMED - DEPARTAMENTO DE CIRURGIA
local.publisher.initialsUFMG
local.url.externahttps://doi:10.14534/pucr.2016316895

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