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Congenital lobar emphysema mimicking as persistent pneumonia in a newborn

Congenital lobar emphysema (CLE) is an uncommon congenital malformation of the lung that can present with respiratory distress in early life. We report a full term female baby who presented with intermittent bluish discoloration of the lips and extremities during crying since birth. An initial diagn...

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Autores principales: Basu, Sriparna, Gupta, Aditya Kumar, Kumar, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981437/
https://www.ncbi.nlm.nih.gov/pubmed/24765342
http://dx.doi.org/10.4081/cp.2011.e101
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author Basu, Sriparna
Gupta, Aditya Kumar
Kumar, Ashok
author_facet Basu, Sriparna
Gupta, Aditya Kumar
Kumar, Ashok
author_sort Basu, Sriparna
collection PubMed
description Congenital lobar emphysema (CLE) is an uncommon congenital malformation of the lung that can present with respiratory distress in early life. We report a full term female baby who presented with intermittent bluish discoloration of the lips and extremities during crying since birth. An initial diagnosis of left sided collapse-consolidation with right-sided compensatory emphysema was made from chest x-ray. When no improvement was noted after intravenous antibiotic therapy for 7 days, computerized tomographic scan of thorax was done which showed emphysema of the right middle lobe with transherniation and mediastinal shift to the left. Right middle lobectomy was done and postoperative period was uneventful. Histopathological examination of the specimen confirmed the diagnosis of CLE. CLE can mimic more common causes of respiratory distress in neonatal period and needs a high index of suspicion for diagnosis. Early diagnosis and effective surgical treatment is curative.
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spelling pubmed-39814372014-04-24 Congenital lobar emphysema mimicking as persistent pneumonia in a newborn Basu, Sriparna Gupta, Aditya Kumar Kumar, Ashok Clin Pract Case Report Congenital lobar emphysema (CLE) is an uncommon congenital malformation of the lung that can present with respiratory distress in early life. We report a full term female baby who presented with intermittent bluish discoloration of the lips and extremities during crying since birth. An initial diagnosis of left sided collapse-consolidation with right-sided compensatory emphysema was made from chest x-ray. When no improvement was noted after intravenous antibiotic therapy for 7 days, computerized tomographic scan of thorax was done which showed emphysema of the right middle lobe with transherniation and mediastinal shift to the left. Right middle lobectomy was done and postoperative period was uneventful. Histopathological examination of the specimen confirmed the diagnosis of CLE. CLE can mimic more common causes of respiratory distress in neonatal period and needs a high index of suspicion for diagnosis. Early diagnosis and effective surgical treatment is curative. PAGEPress Publications 2011-11-07 /pmc/articles/PMC3981437/ /pubmed/24765342 http://dx.doi.org/10.4081/cp.2011.e101 Text en ©Copyright S. Basu et al., 2011 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Case Report
Basu, Sriparna
Gupta, Aditya Kumar
Kumar, Ashok
Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title_full Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title_fullStr Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title_full_unstemmed Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title_short Congenital lobar emphysema mimicking as persistent pneumonia in a newborn
title_sort congenital lobar emphysema mimicking as persistent pneumonia in a newborn
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981437/
https://www.ncbi.nlm.nih.gov/pubmed/24765342
http://dx.doi.org/10.4081/cp.2011.e101
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