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Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts

The standard treatment for the hydrocephalus is ventriculoperitoneal shunts (VPS) operation that diverts the excess accumulated cerebrospinal fluid (CSF) from the ventricles or other CSF containing spaces to another area. The VPS operation has been reportedly associated with risk factor for differen...

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Autores principales: Saeidi Borojeni, Hamid Reza, Fakheri, Taravat, Saeidi Borojeni, Sepehr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kermanshah University of Medical Sciences 2012
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571606/
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author Saeidi Borojeni, Hamid Reza
Fakheri, Taravat
Saeidi Borojeni, Sepehr
author_facet Saeidi Borojeni, Hamid Reza
Fakheri, Taravat
Saeidi Borojeni, Sepehr
author_sort Saeidi Borojeni, Hamid Reza
collection PubMed
description The standard treatment for the hydrocephalus is ventriculoperitoneal shunts (VPS) operation that diverts the excess accumulated cerebrospinal fluid (CSF) from the ventricles or other CSF containing spaces to another area. The VPS operation has been reportedly associated with risk factor for different organs due to peritoneal catheter migration including umbilicus, anus, vagina, mouth, intestine, internal jugular vein, chest, liver. CASE: A 45-day-old male infant was admitted to emergency department of Imam Reza hospital (Kermanshah Iran) with a history of fever, restlessness, leakage of clear fluid through diaper from 2 days ago which exited; appearing from tip of the white tube extruding from scrotum. The infant was born with the myelomeningocele and paraplegia. Therefore, he had previously undergone a surgery at the age of 3 days. One week later the infant developed progressive hydrocephalus and a medium–pressure VP shunt was inserted. He was discharged 3 days later with good health condition and the sutures were removed 12 days later. After a month the infant was brought to the emergency department in ill condition with the symptoms described above. At the PE fever detected and wet diaper was seen and by shunt pump compression clear fluid emerged from the tip of catheter. The CSF analysis revealed meningitis, no growth of pathologic organism 48 hours post-culture. The patient was hospitalized and appropriate antibiotic treatment was started. 10 days later CSF became acellular and the shunt was removed and another VP shunt was inserted contralaterally. After 4 days scrotal orifice was cured and the infant discharged. Previous stories have reported many VS shunt-associated complications such as mechanical failure, functional failure, infections, obstruction, disconnection, migration, hematoma, and slit ventricle syndrome. Mechanical failures consist of obstruction, fracture, disconnection, migration. A search performed in the PubMed showed that until 2006 there has been no report of any case of scrotal skin perforation. Removing the shunt or replacing it with another one can be a good option for the management of any VS shunt failure. In case of leaking fluid, proximal diversion is recommended, while following the treatment of any infection, a new shunt insertion in another site is recommended. KEYWORDS: Hydrocephalus, Ventriculoperitoneal shunt, Infant, Scrotal perforation, Peritoneal catheter
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spelling pubmed-35716062013-03-19 Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts Saeidi Borojeni, Hamid Reza Fakheri, Taravat Saeidi Borojeni, Sepehr J Inj Violence Res Poster Presentation The standard treatment for the hydrocephalus is ventriculoperitoneal shunts (VPS) operation that diverts the excess accumulated cerebrospinal fluid (CSF) from the ventricles or other CSF containing spaces to another area. The VPS operation has been reportedly associated with risk factor for different organs due to peritoneal catheter migration including umbilicus, anus, vagina, mouth, intestine, internal jugular vein, chest, liver. CASE: A 45-day-old male infant was admitted to emergency department of Imam Reza hospital (Kermanshah Iran) with a history of fever, restlessness, leakage of clear fluid through diaper from 2 days ago which exited; appearing from tip of the white tube extruding from scrotum. The infant was born with the myelomeningocele and paraplegia. Therefore, he had previously undergone a surgery at the age of 3 days. One week later the infant developed progressive hydrocephalus and a medium–pressure VP shunt was inserted. He was discharged 3 days later with good health condition and the sutures were removed 12 days later. After a month the infant was brought to the emergency department in ill condition with the symptoms described above. At the PE fever detected and wet diaper was seen and by shunt pump compression clear fluid emerged from the tip of catheter. The CSF analysis revealed meningitis, no growth of pathologic organism 48 hours post-culture. The patient was hospitalized and appropriate antibiotic treatment was started. 10 days later CSF became acellular and the shunt was removed and another VP shunt was inserted contralaterally. After 4 days scrotal orifice was cured and the infant discharged. Previous stories have reported many VS shunt-associated complications such as mechanical failure, functional failure, infections, obstruction, disconnection, migration, hematoma, and slit ventricle syndrome. Mechanical failures consist of obstruction, fracture, disconnection, migration. A search performed in the PubMed showed that until 2006 there has been no report of any case of scrotal skin perforation. Removing the shunt or replacing it with another one can be a good option for the management of any VS shunt failure. In case of leaking fluid, proximal diversion is recommended, while following the treatment of any infection, a new shunt insertion in another site is recommended. KEYWORDS: Hydrocephalus, Ventriculoperitoneal shunt, Infant, Scrotal perforation, Peritoneal catheter Kermanshah University of Medical Sciences 2012-11 /pmc/articles/PMC3571606/ Text en Copyright © 2012, KUMS http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Presentation
Saeidi Borojeni, Hamid Reza
Fakheri, Taravat
Saeidi Borojeni, Sepehr
Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title_full Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title_fullStr Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title_full_unstemmed Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title_short Scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
title_sort scrotal perforation of peritoneal catheter: a rare complication of ventriculoperitoneal shunts
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571606/
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