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Soft tissue sarcomas and central nervous system tumors in children with neurofibromatosis type 1

✍ Scribed by Emre Cecen; Dilek Ince; Kamer Mutafoglu Uysal; Erdener Ozer; Riza Cetingoz; Ali Aykan Ozguven; Handan Cakmakci; Faik Sarialioglu; Nur Olgun

Publisher
Springer
Year
2011
Tongue
English
Weight
408 KB
Volume
27
Category
Article
ISSN
0256-7040

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## Abstract ## BACKGROUND Patients affected by neurofibromatosis type 1 (NF1) are at higher risk of developing soft‐tissue sarcomas (STS) than the general population. The clinical findings and outcome in 43 children and adolescents with NF1 treated for STS in the Italian protocols between 1988 and

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We report the results of the reevaluation of 24 patients with neurofibromatosis type 1 (NF1) using central nervous system (CNS) imaging techniques. The first examination by computed tomography (CT) or magnetic resonance imaging (MRI) indicated the presence of optic glioma in three cases, "unidentifi