scholarly journals INSM1 Expression Is Frequent in Primary Central Nervous System Neoplasms but Not in the Adult Brain Parenchyma

2018 ◽  
Vol 77 (5) ◽  
pp. 374-382 ◽  
Author(s):  
Heather M Ames ◽  
Lisa M Rooper ◽  
John J Laterra ◽  
Charles G Eberhart ◽  
Fausto J Rodriguez
Cancers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 114 ◽  
Author(s):  
Lobbous ◽  
Bernstock ◽  
Coffee ◽  
Friedman ◽  
Metrock ◽  
...  

Neurofibromatosis type 1 (NF1) is an autosomal dominant tumor predisposition syndrome that affects children and adults. Individuals with NF1 are at high risk for central nervous system neoplasms including gliomas. The purpose of this review is to discuss the spectrum of intracranial gliomas arising in individuals with NF1 with a focus on recent preclinical and clinical data. In this review, possible mechanisms of gliomagenesis are discussed, including the contribution of different signaling pathways and tumor microenvironment. Furthermore, we discuss the recent notable advances in the developing therapeutic landscape for NF1-associated gliomas including clinical trials and collaborative efforts.


Author(s):  
J. Bradley Elder ◽  
Ahmed Mohyeldin

Tumors of the spine that occur within the dura but outside of the spinal cord are characterized as intradural but extramedullary spine tumors. The vast majority of these tumors are benign. This chapter uses a case presentation to present diagnostic and management pearls for this anatomic category of central nervous system neoplasms. These tumors are typically diagnosed due to presenting symptoms including pain or neurologic symptoms that localize the tumor to a specific area of the spine. Management is typically surgical. Some types of tumors are associated with syndromes such as neurofibromatosis. This chapter also discusses potential pitfalls and complications and their management.


1999 ◽  
Vol 21 (1) ◽  
pp. 19-25 ◽  
Author(s):  
Carol S. Bruggers ◽  
Dan Fults ◽  
Sherrie L. Perkins ◽  
Cheryl M. Coffin ◽  
William L. Carroll

Neurology ◽  
1966 ◽  
Vol 16 (7) ◽  
pp. 680-680 ◽  
Author(s):  
R. C. Rubin ◽  
A. K. Ommaya ◽  
E. S. Henderson ◽  
E. A. Bering ◽  
D. P. Rall

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