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.accessioned2023-05-11T23:52:01Z
dc.date.accessioned2025-09-08T22:49:06Z
dc.date.available2023-05-11T23:52:01Z
dc.date.issued2016
dc.format.mimetypepdf
dc.identifier.doi10.14534/PUCR.2016316895
dc.identifier.issn21482969
dc.identifier.urihttps://hdl.handle.net/1843/53173
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofPediatric Urology Case Reports
dc.rightsAcesso Aberto
dc.subjectCriança
dc.subjectUretra
dc.subjectSaúde do homem
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 two step surgery correction successfully.
local.publisher.countryBrasil
local.publisher.departmentMED - DEPARTAMENTO DE CIRURGIA
local.publisher.initialsUFMG
local.url.externahttps://www.pediatricurologycasereports.com/abstract/association-of-posterior-urethral-valve-with-congenital-lobar-emphysema-a-case-report-68104.html

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