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Congenital laryngomucocoele: a rare cause for CHAOS

dc.contributor.authorCunha, M
dc.contributor.authorJaneiro, P
dc.contributor.authorFernandes, R
dc.contributor.authorCarreiro, H
dc.contributor.authorLaurini, R
dc.date.accessioned2011-08-29T09:34:49Z
dc.date.available2011-08-29T09:34:49Z
dc.date.issued2009
dc.description.abstractCongenital high airway obstruction syndrome (CHAOS) is a rare but life-threatening condition that results from the obstruction of the upper airways. We describe a female newborn, from a Grávida II, Para 0, 36-year-old woman, with a routine ultrasound at 30 weeks’ gestation that showed polyhydramnios. She delivered a live-born female baby at 36 weeks without any dismorphic features but with respiratory distress. Attempts at endotracheal intubation were unsuccessful due to the presence of a mass obstructing the larynx. The reanimation process was stopped after 20 minutes. Post-mortem examination demonstrated the presence of a total occlusion of the larynx by a laryngomucocoele. Laryngocele, a congenital cyst of the larynx, occurs rarely and hardly ever as a cause of CHAOS. What is more, laryngomucocoele has not been previously reported as a cause of CHAOS. These conditions represent a neonatal emergency with reserved prognosis unless diagnosed antenatally allowing for a programmed ex utero intrapartum treatment (EXIT) by performing tracheostomy while maintaining the placental circulation.por
dc.identifier.citationBMJ Case Rep. 2009; 2009 February 27por
dc.identifier.issn1757-790X
dc.identifier.urihttp://hdl.handle.net/10400.10/397
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherBMJ Publising Grouppor
dc.subjectCriançapor
dc.subjectObstrução das vias respiratóriaspor
dc.subjectDoenças da laringepor
dc.subjectLaryngomucocoelepor
dc.subjectCongenital high airway obstruction syndromepor
dc.subjectCHAOSpor
dc.titleCongenital laryngomucocoele: a rare cause for CHAOSpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLondonpor
oaire.citation.titleBMJ Case Reportspor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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