Intrathoracic migration of ventriculo-peritoneal shunt via Morgagni hernia

Paige A Lundy1,2, Michael D Partington3,4,5, Chad A Tuchek3

  • 1Department of Neurological Surgery, University of Kansas, Kansas City, KS, USA. Plundy@kumc.edu.

Insights

A rare case of Morgagni hernia is presented in a 5-month-old infant who initially had pleural migration of a ventriculo-peritoneal shunt. This diagnosis should be considered in infants with respiratory distress and prior shunt complications.

Area of Science:

  • Pediatric Surgery
  • Thoracic Surgery
  • Medical Diagnostics

Background:

  • Ventriculo-peritoneal shunts are used to treat hydrocephalus in infants.
  • Complications such as catheter migration can occur, requiring careful monitoring.
  • Morgagni hernias are congenital diaphragmatic defects, often asymptomatic but can present with respiratory issues.

Observation:

  • A 5-month-old infant presented with respiratory distress.
  • The patient had a history of pleural migration of a ventriculo-peritoneal shunt catheter.
  • Initial symptoms were attributed to shunt complications, delaying definitive diagnosis.

Findings:

  • The infant was diagnosed with a Morgagni hernia.
  • The hernia likely contributed to or caused the respiratory distress.
  • This case highlights a rare presentation of Morgagni hernia in conjunction with shunt complications.

Implications:

  • Morgagni hernia should be considered in the differential diagnosis of infants with unexplained respiratory distress, especially those with a history of shunt procedures.
  • Early recognition and surgical repair of Morgagni hernias are crucial for favorable outcomes.
  • This case underscores the importance of a comprehensive diagnostic approach in complex pediatric cases.