dc.creatorGerman Mühlhausen, M.
dc.creatorScarlett Brethauer, M.
dc.creatorFernando Martínez, R.
dc.creatorYorky Melipillán, A.
dc.date.accessioned2019-03-11T13:03:51Z
dc.date.available2019-03-11T13:03:51Z
dc.date.created2019-03-11T13:03:51Z
dc.date.issued2012
dc.identifierRevista Chilena de Pediatria, Volumen 83, Issue 1, 2018, Pages 73-77
dc.identifier03704106
dc.identifier07176228
dc.identifier10.4067/S0370-41062012000100009
dc.identifierhttps://repositorio.uchile.cl/handle/2250/165535
dc.description.abstractPersistent Interstitial Pulmonary Emphysema (PIPE) is a syndrome characterized by air leak to the perivascular tissue in the lung, affecting newborns with history of mechanical ventilation. It is also characterized by lack of reabsorption of air in the gap in some areas and giant cell formation. Case Report: A 35-week preterm newborn is presented. Moan and retraction were observed, with oxygen requirements. At the hospital, the diagnosis of transient respiratory distress syndrome was done, requiring nasal CPAP support. At 12 hours of life a sudden clinical deterioration was noted, and a tension pneumothorax of the right lung was confirmed. Pneumothorax was drained with chest tube and high frequency ventilation was initiated. A chest X-ray showed reexpansion of right lung and greater confluence baseline images suggesting bronchopneumonia. After discontinuing ventilatory support, 2 chest CT images show a persistent interstitial pulmonary emphysema in the right lung. Patient was discharge
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceRevista Chilena de Pediatria
dc.subjectNewborn
dc.subjectPersistent pulmonary emphysema interstitial
dc.subjectPneumothorax
dc.titlePersistent interstitial pulmonary emphysema in the newborn: Clinical case Enfisema pulmonar intersticial persistente en recién nacido. Caso clínico
dc.typeArtículos de revistas


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