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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6159073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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