[Late diagnosis bilateral congenital diaphragmatic hernia: a case report]

Gisela Salas1, Aixa Reusmann2, Mariano Boglione2

  • 1Unidad de Cuidados Intensivos Neonatales, Hospital de Pediatría S.A.M.I.C. "Prof. Dr. Juan P. Garrahan", Ciudad Autónoma de Buenos Aires, C1245AAM, Argentina. gsalasenator@gmail.com.

Insights

Bilateral congenital diaphragmatic hernia (B-CDH) is rare and often misdiagnosed. This case highlights the importance of considering B-CDH even after initial diagnosis and treatment for unilateral defects.

Area of Science:

  • Pediatric Surgery
  • Congenital Malformations

Background:

  • Congenital diaphragmatic hernia (CDH) is a rare birth defect affecting diaphragm development.
  • While typically unilateral and left-sided, bilateral CDH (B-CDH) is a rarer variant with higher mortality.
  • Right-sided and bilateral defects are associated with increased mortality risks.

Observation:

  • A patient was initially diagnosed and treated for a unilateral right-sided CDH.
  • During a subsequent laparoscopic Ladd procedure at 8 months of age, a previously undetected left-sided CDH was discovered.

Findings:

  • The case presented as a bilateral congenital diaphragmatic hernia (B-CDH).
  • The initial diagnosis of unilateral right CDH was incomplete, masking the presence of a left-sided defect.

Implications:

  • This case underscores the diagnostic challenges associated with B-CDH.
  • It emphasizes the need for thorough evaluation and consideration of bilateral defects in CDH cases, even after initial treatment.
  • Accurate diagnosis of B-CDH is critical for appropriate management and potentially improving patient outcomes.

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