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Cystic intrapulmonary lymphangioma: HRCT findings

W S Kim1, K S Lee, I Kim

  • 1Department of Radiology, Seoul National University College of Medicine, Korea.

Pediatric Radiology
|January 1, 1995
PubMed

Insights

A rare cystic intrapulmonary lymphangioma in an infant presented with pneumothorax. High-resolution CT (HRCT) findings, including associated septal thickening, aid in differentiating this from other cystic lung diseases.

Area of Science:

  • Pediatric Radiology
  • Thoracic Surgery
  • Pulmonology

Background:

  • Cystic intrapulmonary lymphangioma is a rare congenital lung malformation.
  • Infantile respiratory distress and pneumothorax can be presenting symptoms.

Observation:

  • A 6-month-old infant presented with respiratory distress and pneumothorax due to a left lung lesion.
  • Chest radiography revealed a multicystic lesion mimicking congenital cystic adenomatoid malformation.
  • High-resolution CT (HRCT) demonstrated a multiseptate, air-filled cystic lesion in the left hilar area.

Findings:

  • Associated HRCT findings included thickening of interlobular septa and bronchovascular bundles.
  • Peripheral pulmonary vessels were noted within apical cystic lesions in the left lung.
  • HRCT findings correlated with histopathologic examination, confirming the diagnosis.

Implications:

  • Specific HRCT findings may help differentiate cystic intrapulmonary lymphangioma from other cystic lung diseases.
  • This rare entity should be considered in the differential diagnosis of pediatric multicystic lung lesions.
  • Accurate diagnosis is crucial for appropriate management and improved patient outcomes.

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