Cystic lymphangioma of the chest wall: a case report

Norio Yokoigawa1, Masashi Okuno2, A-H Kwon2

  • 1Department of Surgery, Higashi Osaka Hospital, Osaka, Japan.

Insights

Cystic lymphangioma, a rare congenital chest wall tumor in infants, was successfully treated. This case highlights the importance of prompt diagnosis and surgical intervention for pediatric cystic malformations.

Area of Science:

  • Pediatric Surgery
  • Congenital Malformations
  • Diagnostic Imaging

Background:

  • Cystic lymphangioma is a rare congenital cystic malformation, predominantly affecting the pediatric population.
  • While commonly found in the cervix, its occurrence in the chest wall is exceptionally infrequent.
  • Early identification and management are crucial for favorable outcomes in affected children.

Observation:

  • A 2-month-old female infant presented with a progressively enlarging left chest wall tumor noted since birth.
  • Diagnostic imaging, including transillumination and ultrasonography, confirmed a cystic lesion in the left chest wall.
  • The pediatric patient underwent a single-stage surgical resection for the observed chest wall mass.

Findings:

  • Histopathological examination definitively diagnosed the chest wall lesion as a cystic lymphangioma.
  • The surgical intervention successfully removed the congenital cystic malformation.
  • The case underscores the rarity of chest wall cystic lymphangioma in pediatric patients.

Implications:

  • This case report contributes to the limited literature on pediatric chest wall cystic lymphangioma.
  • It emphasizes the need for considering rare diagnoses in pediatric chest wall tumors.
  • Successful surgical resection offers a curative option for this congenital condition.

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