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. 2021 Apr 5;37(5):1449–1459. doi: 10.1007/s00381-021-05148-1

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — Subependymal giant cell astrocytoma (SEGA): axial FLAIR and T1-contrast-enhanced MRI of a 12-year-old girl with known tuberous sclerosis and epilepsy, presenting with new-onset symptoms of increased intracranial pressure. MRI shows multiple cortical tubers, and bilateral SEGA (prominent on the right side) with obstructive hydrocephalus. The child underwent transcortical resection of the tumor and a septostomy. No progression of the left tumor or recurrence of the right tumor is evident over a 6-year follow-up