Complicated Congenital Pulmonary Adenomatoid Malformation Type I following Right Lower Lobectomy: A Case Report

Preeti Basnet1, Anish Joshi1, Saurab Karki2

  • 1Department of Pediatrics, Kathmandu University School of Medical Sciences, Dhulikhel, Kavrepalanchok, Nepal.

Insights

Congenital pulmonary airway malformation (CPAM) can cause serious illness in children. A 4-year-old girl with recurrent infections successfully underwent surgery for type I CPAM, highlighting the need for more research on symptomatic cases.

Area of Science:

  • Pediatric Surgery
  • Pulmonology
  • Medical Imaging

Background:

  • Congenital pulmonary airway malformation (CPAM) is a rare congenital lung defect impacting infants and children.
  • CPAM can lead to significant respiratory issues and mortality, with variable presentation from birth to later in life.
  • Surgical intervention is often necessary but carries risks, particularly in complex or symptomatic cases.

Observation:

  • A 4-year-old female presented with recurrent chest infections.
  • Imaging confirmed type I CPAM with a coexisting infection.
  • The patient underwent a right lower lobe resection via posterolateral thoracotomy.

Findings:

  • The surgical procedure for type I CPAM in this symptomatic pediatric patient was successful.
  • The patient experienced a favorable outcome and recovered well post-operation.
  • This case demonstrates successful management of a symptomatic CPAM case.

Implications:

  • Further research is needed to establish consensus on surgical timing and outcomes for symptomatic CPAM patients.
  • This case contributes to the understanding of surgical management in pediatric CPAM.
  • Effective treatment of symptomatic CPAM can lead to positive patient outcomes.

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