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A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt

Bladder migration and transurethral extrusion is an extremely rare complication of ventriculoperitoneal (VP) shunt. Only eight cases have been reported in the English literature since 1995. We report a case of a 4-year-old boy with cerebral palsy, hydrocephalus, and VP shunted on both sides who pres...

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Autores principales: Al Fauzi, Asra, Djatisoesanto, Wahjoe, Wahyuhadi, Joni, Parenrengi, Muhammad Arifin, Turchan, Agus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437805/
https://www.ncbi.nlm.nih.gov/pubmed/28553396
http://dx.doi.org/10.4103/jpn.JPN_189_16
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author Al Fauzi, Asra
Djatisoesanto, Wahjoe
Wahyuhadi, Joni
Parenrengi, Muhammad Arifin
Turchan, Agus
author_facet Al Fauzi, Asra
Djatisoesanto, Wahjoe
Wahyuhadi, Joni
Parenrengi, Muhammad Arifin
Turchan, Agus
author_sort Al Fauzi, Asra
collection PubMed
description Bladder migration and transurethral extrusion is an extremely rare complication of ventriculoperitoneal (VP) shunt. Only eight cases have been reported in the English literature since 1995. We report a case of a 4-year-old boy with cerebral palsy, hydrocephalus, and VP shunted on both sides who presented with a protruded distal VP shunt from his urethral orifice. The patient was reported for having previous shunt extrusion through the anus. The patient was treated on by a multidisciplinary approach, involving a neurosurgeon and urologist. Shunt removal with simple procedure was smoothly achieved without morbidities. He was discharged home in satisfactory condition.
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spelling pubmed-54378052017-05-26 A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt Al Fauzi, Asra Djatisoesanto, Wahjoe Wahyuhadi, Joni Parenrengi, Muhammad Arifin Turchan, Agus J Pediatr Neurosci Case Report Bladder migration and transurethral extrusion is an extremely rare complication of ventriculoperitoneal (VP) shunt. Only eight cases have been reported in the English literature since 1995. We report a case of a 4-year-old boy with cerebral palsy, hydrocephalus, and VP shunted on both sides who presented with a protruded distal VP shunt from his urethral orifice. The patient was reported for having previous shunt extrusion through the anus. The patient was treated on by a multidisciplinary approach, involving a neurosurgeon and urologist. Shunt removal with simple procedure was smoothly achieved without morbidities. He was discharged home in satisfactory condition. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5437805/ /pubmed/28553396 http://dx.doi.org/10.4103/jpn.JPN_189_16 Text en Copyright: © 2017 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Al Fauzi, Asra
Djatisoesanto, Wahjoe
Wahyuhadi, Joni
Parenrengi, Muhammad Arifin
Turchan, Agus
A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title_full A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title_fullStr A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title_full_unstemmed A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title_short A Rare Case of Repeated Migration and Transurethral Extrusion of Ventriculoperitoneal Shunt
title_sort rare case of repeated migration and transurethral extrusion of ventriculoperitoneal shunt
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437805/
https://www.ncbi.nlm.nih.gov/pubmed/28553396
http://dx.doi.org/10.4103/jpn.JPN_189_16
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