A Case Series Report on Congenital pulmonary airway malformation – antenatal diagnosis and post-natal follow up

  • Guha Roy A Post Graduate Resident in MD Radio-Diagnosis, Nil Ratan Sircar Medical College, WBUHS, West Bengal, India
  • Sahu S Senior Resident, Department of Radio-diagnosis, Nil Ratan Sircar Medical College, Kolkata, West Bengal, India
  • Mandi K Demonstrator, Department of Radiology, Deben Mahato Government Medical College and Hospital, Purulia
Keywords: CPAM, USG, cystic lung lesion, Types of CPAM, respiratory tract infection

Abstract

Congenital pulmonary airway malformation is the most commonly detected congenital lung defect in the ante-natal period. CPAM is a rare developmental, non-hereditary dysplastic lung lesion. No obvious association with maternal age, race or exposure to any given factor could be ascertained. It has an incidence about 1:1500-4000 of all live birth. We present four cases of congenital pulmonary airway malformation: antenatally detected by ultrasound with their follow up in post-natal period. Three of them have normal uneventful post-natal period. One child was normal for six months of age then developed frequent respiratory tract infection.

Key words-CPAM, USG, cystic lung lesion

 

 

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How to Cite
1.
Guha Roy A, Sahu S, Mandi K. A Case Series Report on Congenital pulmonary airway malformation – antenatal diagnosis and post-natal follow up. Int J Med Res Rev [Internet]. 2024Sep.16 [cited 2024Nov.22];12(4):126-31. Available from: https://ijmrr.medresearch.in/index.php/ijmrr/article/view/1485
Issue
Vol 12 No 4 (2024): Jul-Aug
Section
Case Series

Copyright (c) 2024 Author (s). Published by Siddharth Health Research and Social Welfare Society

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