Congenital lobar emphysema: Is surgery routinely necessary

dc.contributor.authorCeran S.
dc.contributor.authorAltuntas B.
dc.contributor.authorSunam G.
dc.contributor.authorBulut I.
dc.date.accessioned2020-03-26T18:06:00Z
dc.date.available2020-03-26T18:06:00Z
dc.date.issued2010
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractCongenital lobar emphysema (CLE) is a rare congenital abnormality characterised by overinflation of a pulmonary lobe. Its aetiology is unknown. The management of CLE has traditionally been surgical. A newborn boy with a birthweight of 2.5 kg was delivered at full-term by caesarian section due to food delivery. There was no marked respiratory distress at birth, and little meconium stained liquor was seen on the skin. The initial diagnosis was meconium aspiration syndrome. After computed tomography of the thorax, CLE was diagnosed. The patient was observed throughout for a week and the CT of the thorax was repeated, which revealed that the emphysema had resolved. The nonoperative approach should be considered in asymptomatic patients with CLE.en_US
dc.identifier.doi10.4103/0189-6725.59360en_US
dc.identifier.endpage37en_US
dc.identifier.issn0189-6725en_US
dc.identifier.issue1en_US
dc.identifier.pmid20098010en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage36en_US
dc.identifier.urihttps://dx.doi.org/10.4103/0189-6725.59360
dc.identifier.urihttps://hdl.handle.net/20.500.12395/25596
dc.identifier.volume7en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofAfrican Journal of Paediatric Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectRare lung diseaseen_US
dc.subjectThoracic surgeryen_US
dc.titleCongenital lobar emphysema: Is surgery routinely necessaryen_US
dc.typeArticleen_US

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