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Updated: Jun 2, 2026

Neuronavigation and Laparoscopy Guided Ventriculoperitoneal Shunt Insertion for the Treatment of Hydrocephalus
Published on: October 14, 2022
Symptomatic vaginal enterocele associated with malfunctioning ventriculoperitoneal shunt and cerebrospinal ascites
Deborah R Karp1, Tazeen Z Rizvi, G Willy Davila
1Section of Urogynecology/Reconstructive Pelvic Surgery, Cleveland Clinic Florida, 2950 Cleveland Clinic Boulevard, Weston, FL 33331, USA. karpd@ccf.org
Insights
Ventriculoperitoneal shunts can rarely cause abdominal pseudocysts in adults. This case highlights a pseudocyst presenting as pelvic organ prolapse, resolved by shunt revision.
Area of Science:
- Neurosurgery
- Gastroenterology
- Urogynecology
Background:
- Ventriculoperitoneal (VP) shunts are neurosurgical devices used to treat hydrocephalus.
- Abdominal pseudocysts are a rare complication of VP shunts in adults.
- Pelvic organ prolapse (POP) is a common condition affecting women.
Observation:
- A case is presented of a patient with a VP shunt who developed a large abdominal pseudocyst.
- The pseudocyst presented unusually as symptomatic pelvic organ prolapse with stage 4 enterocele.
- The patient's prolapse symptoms worsened as the intra-abdominal cyst enlarged.
Findings:
- VP shunt malfunction can manifest with abdominal complications, including pseudocyst formation.
- Abdominal pseudocysts can present with symptoms mimicking pelvic organ prolapse.
- Conservative management and VP shunt revision/removal resolved the patient's POP and pseudocyst.
Implications:
- Clinicians should consider VP shunt complications in patients with unexplained abdominal symptoms or POP.
- Unusual presentations of VP shunt complications require a high index of suspicion.
- Management of VP shunt-related pseudocysts may involve surgical intervention on the shunt system.
Abstract:
Abdominal pseudocyst formation is a rare adult complication associated with ventriculoperitoneal (VP) shunts. Presenting symptoms are primarily abdominal and include distention, pain and anorexia, and secondarily neurological with signs and symptoms of shunt malfunction. We describe a case of VP shunt-related pseudocyst formation presenting as symptomatic pelvic organ prolapse with stage 4 enterocele 4 years after VP shunt placement. The patient's vaginal enterocele enlarged and became more symptomatic as intra-abdominal cyst formation expanded. Symptomatic relief of pelvic floor symptomatology including resolution of exteriorized prolapse was established by conservative measures and eventual VP shunt revision and removal. VP shunt malfunction may present as symptomatic pelvic organ prolapse and may require shunt removal or revision for resolution of symptoms.
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