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Congenital esophageal stenosis: a rare case of dysphagia

dc.contributor.authorSerrão, E
dc.contributor.authorSantos, A
dc.contributor.authorGaivão, A
dc.contributor.authorTavares, A
dc.contributor.authorFerreira, S
dc.date.accessioned2012-08-10T12:35:41Z
dc.date.available2012-08-10T12:35:41Z
dc.date.issued2010
dc.description.abstractCongenital esophageal stenosis (CES) is a rare anomaly, resulting from incomplete separation of the respiratory tract from the primitive foregut at the 25th day of life. First clinical signs are abnormalities of the swallowing mechanism caused by the intrinsic narrowing of the esophagus. Diagnosis is usually delayed, requiring an accurate history and high level of suspicion, alongside with an esophagogram. Definite diagnosis is only confirmed by histological examination. Treatment usually involves surgery, depending on the severity, location and type of stenosis. We report the case of an 18 months old toddler diagnosed with CES. The characteristic radiographic and CT features are presented as well as the histology.por
dc.identifier.citationJ Radiol Case Rep. 2010; 4(6):8-14por
dc.identifier.issn1943-0922
dc.identifier.urihttp://hdl.handle.net/10400.10/646
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherEduRad Publishingpor
dc.subjectAtrésia esofágicapor
dc.subjectEstenose esofágicapor
dc.subjectCriançapor
dc.subjectDysphagiapor
dc.subjectEsophageal stenosispor
dc.subjectChildpor
dc.titleCongenital esophageal stenosis: a rare case of dysphagiapor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLexingtonpor
oaire.citation.endPage14por
oaire.citation.startPage8por
oaire.citation.titleJournal of Radiology Case Reportspor
oaire.citation.volume4por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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