Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple café au lait
macules, intertriginous freckling, multiple cutaneous neurofibromas, and learning disability …

Optic pathway glioma (OPG) occurs in as many as one-fifth of individuals with the
neurofibromatosis type 1 (NF1) cancer predisposition syndrome. Generally considered low …

The most common childhood central nervous system (CNS) tumor is pediatric low-grade
glioma (pLGG), representing 30%–40% of all CNS tumors in children. Although there is high …

Type 1 neurofibromatosis (NF1) is a dominantly inherited condition predisposing to tumor
development. Optic pathway glioma (OPG) is the most frequent central nervous system …

Background Pediatric cancers are the leading cause of death by disease in children despite
improved survival rates overall. The contribution of germline genetic susceptibility to …

Introduction Optic pathway gliomas (OPGs) are rare neoplasms in children with an
unpredictable clinical course. There is significant controversy regarding the optimal …

Simple Summary In the current study, we systematically reviewed the literature regarding the
management of optic pathway glioma (OPG). This review will analyze demographics …

Interstitial implantation of radioactive materials (brachytherapy [BT]) has been designed to
protractedly deliver a high radiation dose to a well-defined target volume, while minimizing …

The phakomatoses are a heterogenous group of clinical syndromes characterized by
cutaneous, neurologic, and oncologic manifestations. These neurocutaneous syndromes …

Context Although most sellar lesions are related to pituitary adenomas, the region gives rise
to a variety of neoplasms that can be associated with substantial morbidity and/or mortality …