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Description
A 60-year-old man status post right parieto-occipital ventriculoperitoneal shunt with programmable valve for indication of delayed hydrocephalus after aneurysmal subarachnoid haemorrhage returns to clinic 7 weeks after placement for insidious onset of headaches, confusion and gait imbalance. CT scan of the head without contrast revealed an intraparenchymal pericatheter cystic collection with severe oedema (figure 1). The patient denied systemic signs of illness, and laboratory markers for infection were low. A tap of the shunt reservoir revealed no spontaneous flow and difficulty in aspirating cerebrospinal fluid (CSF). Laboratory analysis of the fluid showed negative Gram stain, normal chemistry profile and cell counts. MRI of the brain showed a simple cyst with significant oedema, but no restricted diffusion or contrast enhancement of the cyst wall (figures 2 and 3). CT of the abdomen was benign, without evidence of pseudocyst or other cause of distal obstruction.
The patient was taken to the operating theatre for exploration of the shunt system with high suspicion for proximal mechanical failure. The proximal catheter was disconnected, and found to have no spontaneous flow of CSF. A new proximal catheter was placed using neuronavigation, and spontaneous flow was observed. The system was interrogated, reconnected and incision closed.
The patient had immediate improvement in symptoms. All cultures were negative. He was discharged home on postoperative day 1. With negative cultures, diagnosis of brain abscess was excluded, and intraparenchymal pericatheter cyst was confirmed, a rare, but known, complication of proximal ventriculoperitoneal shunt failure.1 Follow-up CT scan 6 weeks later demonstrated near-complete resolution of the pericatheter cyst, with improvement in oedema (figure 4).
Learning points
Intraparenchymal pericatheter cyst is a rare complication of shunt failure.
Complete resolution can occur with shunt revision only.
Identification can avoid shunt explantation, craniotomy and multiple surgeries as would be required if treated as a brain abscess.
Footnotes
Contributors DJW contributed in acquisition and editing of the images, and drafting the manuscript. RG contributed in final revision of the manuscript. Both authors contributed in conception and critical revision of the manuscript.
Competing interests None declared.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.