A Ventriculoperitoneal Shunt With Anal Protrusion Causing Meningitis in A Child

Ahmed Basehi1,2,3, Abdullah M Al-Saleh1,2,3, Haitham Almoffarreh1,2,3

  • 1Pediatric Emergency Medicine Department, Ministry of the National Guard - Health Affairs, Riyadh, SAU.

Cureus
|October 26, 2023
PubMed

Insights

A rare complication of ventriculoperitoneal (VP) shunts involves tube migration. This case highlights a VP shunt migrating to the anus, leading to meningitis in a pediatric patient.

Area of Science:

  • Neurosurgery
  • Pediatric Surgery
  • Infectious Diseases

Background:

  • Ventriculoperitoneal (VP) shunts are standard treatments for hydrocephalus, involving frequent neurosurgical procedures.
  • Complications include insertion failure, functional issues, and mechanical failures like shunt migration.
  • Migration into the gastrointestinal or urogenital tracts is a rare but serious complication, potentially causing infection and meningitis.

Observation:

  • A 24-month-old male patient with a VP shunt presented with a rare complication.
  • The shunt tube migrated and protruded from the anus.
  • This unusual presentation was followed by the development of meningitis.

Findings:

  • The case demonstrates an extreme instance of VP shunt mechanical failure.
  • Shunt migration to the anus is a rare but critical event.
  • Ascending infection from migrated shunt components can lead to meningitis.

Implications:

  • This case underscores the importance of vigilance for rare VP shunt complications.
  • Prompt diagnosis and management are crucial for pediatric patients with shunt migration.
  • Understanding such rare events can inform surgical techniques and patient monitoring protocols.