CC BY-NC-ND 4.0 · Asian J Neurosurg 2018; 13(03): 918-920
DOI: 10.4103/ajns.AJNS_35_18
Case Report

Natural history of medulloblastoma in a child with neurofibromatosis type I

Mehdi Golpayegani
Department of Neurosurgery, Shahid Beheshti University of Medical Science, Tehran
,
Farhad Salari
Department of Neurosurgery, Shahid Beheshti University of Medical Science, Tehran
,
Zohreh Habibi
1   Department of Neurosurgery, Children's Hospital Medical Center, Tehran University of Medical Science, Tehran
,
Mousarreza Anbarlouei
1   Department of Neurosurgery, Children's Hospital Medical Center, Tehran University of Medical Science, Tehran
,
Ali Mahdavi
2   Department of Radiology, Tehran University of Medical Science, Tehran
,
Farideh Nejat
1   Department of Neurosurgery, Children's Hospital Medical Center, Tehran University of Medical Science, Tehran
› Author Affiliations

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.



Publication History

Article published online:
14 September 2022

© 2018. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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