Show simple item record

dc.contributor.authorHashemzadeh, S
dc.contributor.authorAslanabadi, S
dc.contributor.authorJafari Rouhi, AH
dc.contributor.authorAzhough, R
dc.contributor.authorKaleibar, NA
dc.date.accessioned2018-08-26T06:33:49Z
dc.date.available2018-08-26T06:33:49Z
dc.date.issued2007
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43846
dc.description.abstractCongenital malformations of the lung are rare and vary widely in their presentation and severity. The most common manifestation of the congenital cystic disease of the lung at newborn and early infancy is respiratory distress. Later on in life, cysts usually lose this compressive character and may remain asymptomatic until infection occurs, while producing cough, dyspnea and thoracic pain. The purpose of this study is to review authors institutional experience of congenital cystic lung disease, with specific reference to diagnosis, treatment, as well as outcome, furthermore, to present some cases with unusual clinical manifestations.
dc.language.isoEnglish
dc.relation.ispartofIndian journal of pediatrics
dc.subjectBronchogenic Cyst
dc.subjectBronchopulmonary Sequestration
dc.subjectCystic Adenomatoid Malformation of Lung, Congenital
dc.subjectFemale
dc.subjectHumans
dc.subjectIncidence
dc.subjectInfant, Newborn
dc.subjectIran
dc.subjectLung
dc.subjectMale
dc.subjectPrognosis
dc.subjectPulmonary Emphysema
dc.subjectRespiratory System Abnormalities
dc.subjectRisk Assessment
dc.titleCongenital malformations of the lung.
dc.typearticle
dc.citation.volume74
dc.citation.issue2
dc.citation.spage192
dc.citation.epage4
dc.citation.indexPubmed


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record