Rare Presentation of Congenital Cystic Adenomatoid Malformation of the Lung

Authors

  • Anubha Sharma Department of Paediatrics, Government Medical College, Amritsar
  • MS Pannu Department of Paediatrics, Government Medical College, Amritsar
  • Neeraj Lata Department of Paediatrics, Government Medical College, Amritsar
  • SPS Dhillon Department of Paediatrics, Government Medical College, Amritsar
  • Narinder Singh Department of Paediatrics, Government Medical College, Amritsar
  • Ashwini Sareen Department of Paediatrics, Government Medical College, Amritsar

DOI:

https://doi.org/10.3126/jnps.v36i1.13159

Keywords:

CCAM, CPAM, Pneumothorax

Abstract

Congenital cystic adenomatoid malformation is a rare entity presenting with respiratory difficulty in newborns and even later in infancy. Various cases have been reported but recurrent spontaneous pneumothorax in an infant with failure to thrive and pectus carinatum since birth(with uneventful antenatal history and asymptomatic course in the first seven months of life) is an extremely rare presentation of this congenital lung condition.

J Nepal Paediatr Soc 2016;36(1):91-93.

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Author Biographies

Anubha Sharma, Department of Paediatrics, Government Medical College, Amritsar

Senior Resident

MS Pannu, Department of Paediatrics, Government Medical College, Amritsar

Professor and HoD Paediatrics

Neeraj Lata, Department of Paediatrics, Government Medical College, Amritsar

Senior Resident

SPS Dhillon, Department of Paediatrics, Government Medical College, Amritsar

Assistant Professor

Narinder Singh, Department of Paediatrics, Government Medical College, Amritsar

Assistant Professor

Ashwini Sareen, Department of Paediatrics, Government Medical College, Amritsar

Associate Professor

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Published

2016-10-22

How to Cite

Sharma, A., Pannu, M., Lata, N., Dhillon, S., Singh, N., & Sareen, A. (2016). Rare Presentation of Congenital Cystic Adenomatoid Malformation of the Lung. Journal of Nepal Paediatric Society, 36(1), 91–93. https://doi.org/10.3126/jnps.v36i1.13159

Issue

Section

Brief Reports/Case Reports/Case Series