Persistent interstitial pulmonary emphysema in the newborn: Clinical case Enfisema pulmonar intersticial persistente en recién nacido. Caso clínico
Author
dc.contributor.author
German Mühlhausen, M.
Author
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Scarlett Brethauer, M.
Author
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Fernando Martínez, R.
Author
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Yorky Melipillán, A.
Admission date
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2019-03-11T13:03:51Z
Available date
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2019-03-11T13:03:51Z
Publication date
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2012
Cita de ítem
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Revista Chilena de Pediatria, Volumen 83, Issue 1, 2018, Pages 73-77
Identifier
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03704106
Identifier
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07176228
Identifier
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10.4067/S0370-41062012000100009
Identifier
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https://repositorio.uchile.cl/handle/2250/165535
Abstract
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Persistent 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