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Neuronavigation and Laparoscopy Guided Ventriculoperitoneal Shunt Insertion for the Treatment of Hydrocephalus
Published on: October 14, 2022
Bowel perforation secondary to ventriculoperitoneal shunt: case report and clinical analysis
1Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, People's Republic of China.
Insights
Bowel perforation is a rare complication of ventriculoperitoneal shunts. This case highlights successful management of a shunt tube protruding through the anus in an infant.
Area of Science:
- Pediatric Surgery
- Neurosurgery
- Gastrointestinal Surgery
Background:
- Ventriculoperitoneal shunts are common for hydrocephalus and meningocoele.
- Bowel perforation is an infrequent but serious complication.
Observation:
- An 8-month-old infant with a ventriculoperitoneal shunt presented with the distal tube protruding from the anus.
- No signs of meningitis or peritonitis were observed.
Findings:
- Laparotomy revealed the shunt tube entering the transverse colon, encapsulated by the omentum.
- The tube was transected, the distal end removed rectally, and the colon repaired.
- The shunt remained functional, and the infant was asymptomatic post-procedure.
Implications:
- This case demonstrates a rare shunt complication and its successful surgical resolution.
- Early recognition and intervention are crucial for managing shunt-related bowel perforation.
- Reviewing therapeutic options is essential for optimizing patient outcomes in similar cases.
Abstract:
Bowel perforation is an unusual complication of ventriculoperitoneal shunting. This article describes a case of bowel perforation associated with a ventriculoperitoneal shunt inserted in an 8-month-old male infant for meningocoele and hydrocephalus. Ten months after insertion of the shunt the infant presented with the shunting tube protruding through the anus. There were no signs of meningitis or peritonitis. At laparotomy the tube was seen to enter the transverse colon and was encapsulated by the greater omentum. The tube was cut and the distal end removed via the anus. The transverse colon was repaired. The catheter continued to function effectively and the patient remained asymptomatic. The literature on this rare complication is reviewed and the therapeutic options are discussed.
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