Congenital Pulmonary Airway Malformation with Pulmonary Arteriovenous Malformation in Adulthood: A Case Report

Takehiro Suzuki1, Naohiro Kobayashi1, Yohei Yatagai2

  • 1Department of General Thoracic Surgery, Tsukuba University Hospital, Tsukuba, Ibaraki, Japan.

PubMed

Insights

This study reports a rare adult case of coexisting congenital pulmonary airway malformation (CPAM) and pulmonary arteriovenous malformation (PAVM). Surgical intervention was successful in managing the coexisting conditions and preventing complications.

Area of Science:

  • Pulmonology
  • Thoracic Surgery
  • Medical Imaging

Background:

  • Congenital pulmonary airway malformation (CPAM) is typically diagnosed in infancy or childhood.
  • Pulmonary arteriovenous malformation (PAVM) is an abnormal vascular connection often linked to hereditary hemorrhagic telangiectasia.
  • Coexistence of CPAM and PAVM is exceptionally rare in adults.

Observation:

  • A 26-year-old woman presented with incidentally discovered lung abnormalities.
  • Chest CT revealed multiple lung cysts (suspected CPAM Type 1) and two PAVMs in the left lower lobe.
  • Pulmonary aspergillosis was diagnosed and treated, but one PAVM enlarged during treatment.

Findings:

  • Surgical resection (left lower lobectomy) was performed due to uncontrolled infection and PAVM enlargement.
  • Pathological diagnosis confirmed CPAM Type 1.
  • The patient experienced no complications post-surgery.

Implications:

  • Simultaneous CPAM and PAVM in adults is a rare clinical entity.
  • Pulmonary infections associated with CPAM may contribute to PAVM development or enlargement.
  • Surgical management should be considered for coexisting CPAM and PAVM to prevent serious complications.
Abstract

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