ArticleJournal of clinical and diagnostic research : JCDR2015
Intraabdominal Pseudocyst Developed after Ventriculoperitoneal Shunt: A Case Report.
Article in Journal of clinical and diagnostic research : JCDR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 13 citations in OpenAlex.
- Rare case of intraperitoneal cerebrospinal fluid pseudocyst secondary to ventriculoperitoneal shunt: A case report and literature review.Surgical neurology international · 2026Article
- Abdominal complications in patients with a ventriculoperitoneal shunt: proposal for management recommendations from a single pediatric tertiary center.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
- Abdominal Complications Related to Ventriculoperitoneal Shunt Placement: A Comprehensive Review of Literature.Cureus · 2021Review
- Case Series of Ventriculoatrial Shunt placement in Hybrid Room: Reassessment of Ventriculoatrial Shunt.Korean journal of neurotrauma · 2020Article
- Huge abdominal cerebrospinal fluid pseudocyst following ventriculoperitoneal shunt: a case report.Journal of medical case reports · 2019Article
- Laparoscopic management of abdominal pseudocyst following ventriculoperitoneal shunt implantation in hydrocephalus.Wideochirurgia i inne techniki maloinwazyjne = Videosurgery and other miniinvasive techniques · 2018Article
- Treatment of abdominal pseudocysts and associated ventricuoperitoneal shunt failure.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Abdominal pseudocyst is a rare complication developing after ventriculoperitoneal shunt treatment. It is more commonly seen particularly in children. The underlying pathogenesis may be associated with repeat revisions or infections. Morphologically, it has no complete cyst wall, presenting only with a pseudocapsule among the intestinal loops, around the lower shunt tip. The principal problem appears to be the reduced peritoneal absorption capacity. The treatment is complicated and difficult. In this report, we present an 8-year-old abdominal pseudocyst case with a history of many shunt revisions.
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Registered trials
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