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February 22, 2026Surgical Neurology International0 citations

Ventriculoperitoneal shunt-associated cystic lesion with perilesional cerebral edema 45 years after placement for posterior fossa tumor: A case report

KSKohei SatoRHRyusuke HataeRORyosuke Otsuji

Key Points

  • To report a unique case of a cystic lesion developing 45 years after ventriculoperitoneal shunt placement for hydrocephalus.
  • Case report of a 58-year-old man with a history of VP shunt placement.
  • Neuroimaging was used to analyze the cystic lesion and edema.
  • Retrospective review of previous MRI performed 3 months earlier.
  • Identification of a right frontal low-density lesion with vasogenic edema and cystic cavity.
  • Removal of the shunt catheter revealed obstruction due to membranous material.
  • Post-surgery, the patient's hemiparesis improved and follow-up imaging showed reduced cyst size and edema.

Abstract

Background: Ventriculoperitoneal (VP) shunts are widely used to treat hydrocephalus in children with posterior fossa tumors. While many patients gain shunt independence after tumor control, indwelling shunts are often not removed. Shunt-related intracranial cysts are extremely rare and typically develop along the intracranial catheter tract within days to several years after shunt insertion; to date, the longest reported interval has been 19 years. Here, we report a case a cystic lesion with marked perilesional edema developing 45 years after childhood VP shunt placement for tumor-related hydrocephalus. Case Description: We report the case of a 58-year-old man who presented with acute severe left-sided hemiparesis. At the age of 13 years, he underwent resection of a posterior fossa ependymoma, VP shunt placement, and whole-brain radiotherapy. Neuroimaging revealed a large right frontal low-density lesion with vasogenic edema and a cystic cavity surrounding the intracranial shunt catheter. Retrospective review of magnetic resonance imaging performed 3 months earlier showed a smaller preexisting cyst at the same site. The shunt catheter was removed without resistance, and the membranous material adhering to the distal tip caused partial intraluminal obstruction. Postoperatively, the hemiparesis improved markedly; follow-up imaging demonstrated resolution of the edema and reduction in the cyst size. As hydrocephalus did not recur, shunt reinsertion was not required. Conclusion: This case represents the longest latency reported in the literature for VP shunt-related intracranial cyst formation, occurring 45 years after shunt implantation, exceeding the previously reported maximum interval of 19 years. The acute symptoms closely resemble stroke or infection, underscoring the diagnostic challenge. Clinicians should be vigilant of such delayed complications even decades after shunt placement.

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Cite This Study

Sato et al. (2026) studied this question.

synapsesocial.com/papers/699a9d7a482488d673cd36c7https://doi.org/10.25259/sni_1135_2025
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Cerebral Parenchymal Cyst: A Rare Complication of Ventriculoperitoneal Shunt Malfunction2026
  2. 2Abdominal wall CSF pseudocyst following ventriculoperitoneal shunt displacement: a case report and literature review2025
  3. 3From Brain to Belly: A Giant Pseudocyst as a Rare Sequela of Ventriculoperitoneal Shunt2026
  4. 4Recurrent abdominal CSF pseudocysts: a rare complication of Ventriculo-peritoneal shunt2016
  5. 5Shunt-related brain tumor, a case report presenting a rare complication and review of literature2024