An unusual tuberous sclerosis case presenting with fibrillary astrocytoma
Özet
Tuberous sclerosis (TS) is an autosomal dominant disorder. It is characterized by hamartomatous lesions in various organs such as the brain, skin, kidneys and heart. Subependymal and parenchymal nodules occur in the cerebrum. Although giant cell astrocytoma may develop from these subependymal nodules, tumor formation is very rare in the cortical nodules. We present the clinical, computed tomography and magnetic resonance imaging findings of a fibrillary astrocytoma originating from a cortical tuber in a 4-year-old female with TS. Copyright (C) 2002 S. Karger AG, Basel.
Atıf için künye
Eren, S., Polat, P., & Erman, Z. (2002). An unusual tuberous sclerosis case presenting with fibrillary astrocytoma. PEDIATRIC NEUROSURGERY, 37(3), 118–121. https://doi.org/10.1159/000064397
BibTeX
@article{eren2002-230947,
author = {Eren, Suat and Polat, P and Erman, Z},
title = {An unusual tuberous sclerosis case presenting with fibrillary astrocytoma},
journal = {PEDIATRIC NEUROSURGERY},
year = {2002},
volume = {37},
number = {3},
pages = {118--121},
issn = {1016-2291},
doi = {10.1159/000064397},
url = {https://akademik.atauni.edu.tr/yayinlar/230947-an-unusual-tuberous-sclerosis-case-presenting-with-fibrillary-astrocytoma}
}