Intraperitoneal cerebrospinal fluid pseudocyst. A rare complication of ventriculoperitoneal shunt

Th Birbilis1, K Kontogianidis, G Matis

  • 1Department of Neurosurgery, University Hospital of Alexandroupolis, Democritus University of Thrace Medical School, Alexandroupolis, Greece. mpirmpil@otenet.gr

Chirurgia (Bucharest, Romania : 1990)
|August 23, 2008
PubMed

Insights

A rare complication of ventriculoperitoneal shunts, abdominal cerebrospinal fluid pseudocysts can occur. This case highlights a large pseudocyst treated successfully by catheter repositioning and antibiotics.

Area of Science:

  • Neurosurgery
  • Pediatric Surgery
  • Infectious Diseases

Background:

  • Ventriculoperitoneal shunts are common treatments for hydrocephalus.
  • Abdominal cerebrospinal fluid pseudocysts are rare but significant complications.
  • These pseudocysts can arise from shunt malfunction or infection.

Observation:

  • A 31-year-old female presented with a large abdominal pseudocyst one year post-ventriculoperitoneal shunt insertion.
  • Imaging revealed a 50 cm3 cystic mass in the hepato-renal recess, containing the shunt's peritoneal tip.
  • Cerebrospinal fluid culture identified Staphylococcus epidermis infection.

Findings:

  • Distal externalization of the peritoneal catheter, without pseudocyst excision, was performed.
  • Antibiotic treatment targeted the identified Staphylococcus epidermis infection.
  • Symptoms resolved within 4 weeks, and a new shunt catheter was placed in a different abdominal quadrant.

Implications:

  • This case demonstrates a successful management strategy for abdominal cerebrospinal fluid pseudocysts.
  • Chronic inflammation or subclinical peritonitis may predispose patients to this complication.
  • Further research into preventative measures and optimal treatment protocols is warranted.

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