Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion

Key Clinical Message Abdominal pseudocyst is a rare complication of ventriculoperitoneal (VP) shunt placement. Ventriculopleural shunt (VPL) can be an effective treatment option for the recurrent complications of VP shunt failure. Abstract Abdominal pseudocyst (APC) is a rare complication of ventric...

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Main Authors: Nishan Shrestha, Naveen Gautam, Merina Shrestha
Format: Article
Language:English
Published: Wiley 2023-09-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.7902
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author Nishan Shrestha
Naveen Gautam
Merina Shrestha
author_facet Nishan Shrestha
Naveen Gautam
Merina Shrestha
author_sort Nishan Shrestha
collection DOAJ
description Key Clinical Message Abdominal pseudocyst is a rare complication of ventriculoperitoneal (VP) shunt placement. Ventriculopleural shunt (VPL) can be an effective treatment option for the recurrent complications of VP shunt failure. Abstract Abdominal pseudocyst (APC) is a rare complication of ventriculoperitoneal (VP) shunt placement for the treatment of congenital hydrocephalus. This case report presents a two‐and‐a‐half‐year‐old male child who underwent VP shunt placement for aqueductal stenosis‐related hydrocephalus. The patient subsequently developed recurrent shunt failure and an APC, which was managed initially by surgical excision of the cyst and repositioning of the catheter. However, shunt failure recurred. The patient underwent ventriculopleural (VPL) shunt conversion as a more viable option for recurrent blockage. Postoperatively, the patient developed respiratory distress with massive pleural effusion, which was treated with chest tube insertion. This case highlights the complexity of managing congenital hydrocephalus and its rare complication, APC. Prompt recognition and appropriate management of APC can lead to improved outcomes and minimize the need for invasive procedures. VPL shunt conversion can be considered an alternative treatment option when other treatments have failed. Further research is needed to establish guidelines for the management of APC and determine the long‐term effectiveness of VPL shunting.
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spelling doaj.art-63bc3cf47b92418b871c28c54560f0e12023-10-20T06:16:22ZengWileyClinical Case Reports2050-09042023-09-01119n/an/a10.1002/ccr3.7902Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversionNishan Shrestha0Naveen Gautam1Merina Shrestha2Intern doctor Tribhuvan University Teaching Hospital Kathmandu NepalIntern doctor Tribhuvan University Teaching Hospital Kathmandu NepalPaediatrics Tribhuvan University Teaching Hospital Kathmandu NepalKey Clinical Message Abdominal pseudocyst is a rare complication of ventriculoperitoneal (VP) shunt placement. Ventriculopleural shunt (VPL) can be an effective treatment option for the recurrent complications of VP shunt failure. Abstract Abdominal pseudocyst (APC) is a rare complication of ventriculoperitoneal (VP) shunt placement for the treatment of congenital hydrocephalus. This case report presents a two‐and‐a‐half‐year‐old male child who underwent VP shunt placement for aqueductal stenosis‐related hydrocephalus. The patient subsequently developed recurrent shunt failure and an APC, which was managed initially by surgical excision of the cyst and repositioning of the catheter. However, shunt failure recurred. The patient underwent ventriculopleural (VPL) shunt conversion as a more viable option for recurrent blockage. Postoperatively, the patient developed respiratory distress with massive pleural effusion, which was treated with chest tube insertion. This case highlights the complexity of managing congenital hydrocephalus and its rare complication, APC. Prompt recognition and appropriate management of APC can lead to improved outcomes and minimize the need for invasive procedures. VPL shunt conversion can be considered an alternative treatment option when other treatments have failed. Further research is needed to establish guidelines for the management of APC and determine the long‐term effectiveness of VPL shunting.https://doi.org/10.1002/ccr3.7902abdominal pseudocystcongenital hydrocephalusventriculoperitoneal shuntventriculopleural shunt
spellingShingle Nishan Shrestha
Naveen Gautam
Merina Shrestha
Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
Clinical Case Reports
abdominal pseudocyst
congenital hydrocephalus
ventriculoperitoneal shunt
ventriculopleural shunt
title Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
title_full Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
title_fullStr Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
title_full_unstemmed Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
title_short Abdominal pseudocyst complicating ventriculoperitoneal shunt: A rare indication for ventriculopleural shunt conversion
title_sort abdominal pseudocyst complicating ventriculoperitoneal shunt a rare indication for ventriculopleural shunt conversion
topic abdominal pseudocyst
congenital hydrocephalus
ventriculoperitoneal shunt
ventriculopleural shunt
url https://doi.org/10.1002/ccr3.7902
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AT naveengautam abdominalpseudocystcomplicatingventriculoperitonealshuntarareindicationforventriculopleuralshuntconversion
AT merinashrestha abdominalpseudocystcomplicatingventriculoperitonealshuntarareindicationforventriculopleuralshuntconversion