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Hydrocephalus in children – A rare case of pineal cavernoma and literature review
BACKGROUND: Cavernous malformations prevalence ranges from 0.4 to 0.6% and accounts for 5–15% of all central nervous system vascular malformations. Pineal cavernomas constitute <1% of all locations published in the literature, with a total of 26 cases reported, only 5 regarding the pediatric popu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568112/ https://www.ncbi.nlm.nih.gov/pubmed/33093971 http://dx.doi.org/10.25259/SNI_231_2020 |
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author | Nogueira, Ricardo Malcata Cardoso, Luis Santos Fonseca, Lino Correia, Miguel Iraneta, Amets Roque, Pedro Matos, Mario Mafra, Manuela |
author_facet | Nogueira, Ricardo Malcata Cardoso, Luis Santos Fonseca, Lino Correia, Miguel Iraneta, Amets Roque, Pedro Matos, Mario Mafra, Manuela |
author_sort | Nogueira, Ricardo Malcata |
collection | PubMed |
description | BACKGROUND: Cavernous malformations prevalence ranges from 0.4 to 0.6% and accounts for 5–15% of all central nervous system vascular malformations. Pineal cavernomas constitute <1% of all locations published in the literature, with a total of 26 cases reported, only 5 regarding the pediatric population until 2020. Overall annual hemorrhage rate is 2.4%. Symptoms are often due to hydrocephalus and intracranial hypertension. CASE DESCRIPTION: We report a case of a 5-year-old child with visual disturbances, headache, and progressive neurologic deterioration. MR showed a lesion in the pineal region and triventricular hydrocephalus. She was submitted to endoscopic third ventriculostomy and total excision of the lesion by the infratentorial supracerebellar approach a few days later. Histopathological examination confirmed a pineal cavernous malformation. The patient returned to her normal life without any neurologic deficit and a normal development. CONCLUSION: The ideal treatment is primary lesion removal; however, due to the infrequency and because it is a curable lesion, studies seeking to deepen the knowledge of this disease are considered relevant. |
format | Online Article Text |
id | pubmed-7568112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-75681122020-10-21 Hydrocephalus in children – A rare case of pineal cavernoma and literature review Nogueira, Ricardo Malcata Cardoso, Luis Santos Fonseca, Lino Correia, Miguel Iraneta, Amets Roque, Pedro Matos, Mario Mafra, Manuela Surg Neurol Int Case Report BACKGROUND: Cavernous malformations prevalence ranges from 0.4 to 0.6% and accounts for 5–15% of all central nervous system vascular malformations. Pineal cavernomas constitute <1% of all locations published in the literature, with a total of 26 cases reported, only 5 regarding the pediatric population until 2020. Overall annual hemorrhage rate is 2.4%. Symptoms are often due to hydrocephalus and intracranial hypertension. CASE DESCRIPTION: We report a case of a 5-year-old child with visual disturbances, headache, and progressive neurologic deterioration. MR showed a lesion in the pineal region and triventricular hydrocephalus. She was submitted to endoscopic third ventriculostomy and total excision of the lesion by the infratentorial supracerebellar approach a few days later. Histopathological examination confirmed a pineal cavernous malformation. The patient returned to her normal life without any neurologic deficit and a normal development. CONCLUSION: The ideal treatment is primary lesion removal; however, due to the infrequency and because it is a curable lesion, studies seeking to deepen the knowledge of this disease are considered relevant. Scientific Scholar 2020-09-18 /pmc/articles/PMC7568112/ /pubmed/33093971 http://dx.doi.org/10.25259/SNI_231_2020 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 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 Nogueira, Ricardo Malcata Cardoso, Luis Santos Fonseca, Lino Correia, Miguel Iraneta, Amets Roque, Pedro Matos, Mario Mafra, Manuela Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title | Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title_full | Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title_fullStr | Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title_full_unstemmed | Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title_short | Hydrocephalus in children – A rare case of pineal cavernoma and literature review |
title_sort | hydrocephalus in children – a rare case of pineal cavernoma and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568112/ https://www.ncbi.nlm.nih.gov/pubmed/33093971 http://dx.doi.org/10.25259/SNI_231_2020 |
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