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Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I

Medulloblastoma is one of the common posterior fossa tumors in children. The natural history of this tumor in presymptomatic period is not well known. Widespread use of brain imaging has increased the detection of incidental brain tumors in totally asymptomatic persons. Here, we report a case of a 4...

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Autores principales: Golpayegani, Mehdi, Salari, Farhad, Habibi, Zohreh, Anbarlouei, Mousarreza, Mahdavi, Ali, Nejat, Farideh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159073/
https://www.ncbi.nlm.nih.gov/pubmed/30283582
http://dx.doi.org/10.4103/ajns.AJNS_35_18
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author Golpayegani, Mehdi
Salari, Farhad
Habibi, Zohreh
Anbarlouei, Mousarreza
Mahdavi, Ali
Nejat, Farideh
author_facet Golpayegani, Mehdi
Salari, Farhad
Habibi, Zohreh
Anbarlouei, Mousarreza
Mahdavi, Ali
Nejat, Farideh
author_sort Golpayegani, Mehdi
collection PubMed
description Medulloblastoma is one of the common posterior fossa tumors in children. The natural history of this tumor in presymptomatic period is not well known. Widespread use of brain imaging has increased the detection of incidental brain tumors in totally asymptomatic persons. Here, we report a case of a 4-year-old boy with prenatal diagnosis of congenital brain abnormalities and neurofibromatosis type I. He underwent regular brain imaging to follow interhemispheric arachnoid cyst and ventriculomegaly that a posterior fossa tumor was discovered. The tumor size increased during time and became symptomatic after 28 months which was resected.
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spelling pubmed-61590732018-10-03 Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I Golpayegani, Mehdi Salari, Farhad Habibi, Zohreh Anbarlouei, Mousarreza Mahdavi, Ali Nejat, Farideh Asian J Neurosurg Case Report Medulloblastoma is one of the common posterior fossa tumors in children. The natural history of this tumor in presymptomatic period is not well known. Widespread use of brain imaging has increased the detection of incidental brain tumors in totally asymptomatic persons. Here, we report a case of a 4-year-old boy with prenatal diagnosis of congenital brain abnormalities and neurofibromatosis type I. He underwent regular brain imaging to follow interhemispheric arachnoid cyst and ventriculomegaly that a posterior fossa tumor was discovered. The tumor size increased during time and became symptomatic after 28 months which was resected. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6159073/ /pubmed/30283582 http://dx.doi.org/10.4103/ajns.AJNS_35_18 Text en Copyright: © 2018 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Golpayegani, Mehdi
Salari, Farhad
Habibi, Zohreh
Anbarlouei, Mousarreza
Mahdavi, Ali
Nejat, Farideh
Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title_full Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title_fullStr Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title_full_unstemmed Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title_short Natural History of Medulloblastoma in a Child with Neurofibromatosis Type I
title_sort natural history of medulloblastoma in a child with neurofibromatosis type i
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6159073/
https://www.ncbi.nlm.nih.gov/pubmed/30283582
http://dx.doi.org/10.4103/ajns.AJNS_35_18
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