Experience of choroid plexus papilloma in children at Mansoura University Hospital

Choroid plexus papilloma (CPP) are rare, benign tumours of neuroectodermal origin; they represent 1-3% of central nervous system (CNS) tumours in paediatric patients. Authors present their experience in the management of such lesion in Mansoura University Hospitals. Methods. For children with Choro...

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Main Authors: Hatem Badr, Ahmad Zaher, Mohamed State, Amr Farid Khalil
Format: Article
Language:English
Published: London Academic Publishing 2019-06-01
Series:Romanian Neurosurgery
Subjects:
Online Access:https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/574
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spelling doaj-294b4b5fd8a149ecb4bb084599690bfa2020-11-25T01:08:09ZengLondon Academic PublishingRomanian Neurosurgery1220-88412344-49592019-06-0133210.33962/roneuro-2019-027Experience of choroid plexus papilloma in children at Mansoura University HospitalHatem BadrAhmad ZaherMohamed StateAmr Farid Khalil Choroid plexus papilloma (CPP) are rare, benign tumours of neuroectodermal origin; they represent 1-3% of central nervous system (CNS) tumours in paediatric patients. Authors present their experience in the management of such lesion in Mansoura University Hospitals. Methods. For children with Choroid plexus papilloma who were treated via microsurgical excision over 4 years from January 2012 to January 2016 in Mansoura University Hospitals, a retrospective analysis was done for age, sex, clinical manifestations, surgical treatment and follow up. Results. Twenty-three paediatrics were treated over 4 years. Age ranged from (7 months - 8 years). There were 13 female and10 males. Tumours were located in the lateral ventricle in all cases. Features of raised intracranial pressure were the predominant presentation. Total microsurgical excision was achieved in all cases. All cases had intraoperative blood loss < 100 ml with mean Haematocrit 28%. Follow up period (7-53 months). Complete relief of all symptoms was reported in all cases with no mortality. One of our patients needs postoperative ventriculoperitoneal shunt for persistent CSF leakage and another one required subdural peritoneal shunt for persistent subdural CSF collection. Conclusion. Total excision of Choroid plexus papilloma is usually the rule with an excellent outcome. Routine external ventricular drainage for at least 3 days is effective in lowering shunt-dependent cases as it allows the release of bloody CSF and small tumour residue. With proper microsurgical technique through superior parietal lobule to access lateral ventricle then tumour coagulation at the same time of irrigation that helps the tumour to shrink and thus, decrease the incidence of bleeding. The tumour vascular pedicle should be resected with the last part of the tumour to avoid pedicle retraction that may lead to ventricular haemorrhage. https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/574choroid plexus papillomasurgical resectioncomplications
collection DOAJ
language English
format Article
sources DOAJ
author Hatem Badr
Ahmad Zaher
Mohamed State
Amr Farid Khalil
spellingShingle Hatem Badr
Ahmad Zaher
Mohamed State
Amr Farid Khalil
Experience of choroid plexus papilloma in children at Mansoura University Hospital
Romanian Neurosurgery
choroid plexus papilloma
surgical resection
complications
author_facet Hatem Badr
Ahmad Zaher
Mohamed State
Amr Farid Khalil
author_sort Hatem Badr
title Experience of choroid plexus papilloma in children at Mansoura University Hospital
title_short Experience of choroid plexus papilloma in children at Mansoura University Hospital
title_full Experience of choroid plexus papilloma in children at Mansoura University Hospital
title_fullStr Experience of choroid plexus papilloma in children at Mansoura University Hospital
title_full_unstemmed Experience of choroid plexus papilloma in children at Mansoura University Hospital
title_sort experience of choroid plexus papilloma in children at mansoura university hospital
publisher London Academic Publishing
series Romanian Neurosurgery
issn 1220-8841
2344-4959
publishDate 2019-06-01
description Choroid plexus papilloma (CPP) are rare, benign tumours of neuroectodermal origin; they represent 1-3% of central nervous system (CNS) tumours in paediatric patients. Authors present their experience in the management of such lesion in Mansoura University Hospitals. Methods. For children with Choroid plexus papilloma who were treated via microsurgical excision over 4 years from January 2012 to January 2016 in Mansoura University Hospitals, a retrospective analysis was done for age, sex, clinical manifestations, surgical treatment and follow up. Results. Twenty-three paediatrics were treated over 4 years. Age ranged from (7 months - 8 years). There were 13 female and10 males. Tumours were located in the lateral ventricle in all cases. Features of raised intracranial pressure were the predominant presentation. Total microsurgical excision was achieved in all cases. All cases had intraoperative blood loss < 100 ml with mean Haematocrit 28%. Follow up period (7-53 months). Complete relief of all symptoms was reported in all cases with no mortality. One of our patients needs postoperative ventriculoperitoneal shunt for persistent CSF leakage and another one required subdural peritoneal shunt for persistent subdural CSF collection. Conclusion. Total excision of Choroid plexus papilloma is usually the rule with an excellent outcome. Routine external ventricular drainage for at least 3 days is effective in lowering shunt-dependent cases as it allows the release of bloody CSF and small tumour residue. With proper microsurgical technique through superior parietal lobule to access lateral ventricle then tumour coagulation at the same time of irrigation that helps the tumour to shrink and thus, decrease the incidence of bleeding. The tumour vascular pedicle should be resected with the last part of the tumour to avoid pedicle retraction that may lead to ventricular haemorrhage.
topic choroid plexus papilloma
surgical resection
complications
url https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/574
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