Ganglioglioma surgery: Difference between revisions
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==Overview== | ==Overview== | ||
==Surgery== | |||
Surgery is the mainstay of treatment for ganglioglioma. Surgical resection of the tumor is associated with good clinical and seizure outcome. Even if the seizure is not entirely cured by resection, the frequency of the seizures with decline significantly. | |||
Total resection is associated with higher rates of local control and survival, but it can be technically challenging due to the unclear border of the tumor. In cases of subtotal resection, adjuvant radiotherapy is helpful. If the resection fails to cure, adjuvant therapy with mTOR inhibitors could be considered. <ref name="">{{cite book | last = Hayat | first = M. A. | title = Tumors of the central nervous system | publisher = Springer | location = Dordrecht New York | year = 2012 | isbn = 978-94-007-5487-4 }}</ref> | |||
==References== | ==References== | ||
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[[Category:Neurology]] | [[Category:Neurology]] | ||
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{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
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Latest revision as of 23:49, 27 August 2019
Ganglioglioma Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Ganglioglioma surgery On the Web |
American Roentgen Ray Society Images of Ganglioglioma surgery |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Mandana Chitsazan, M.D. [2]
Overview
Surgery
Surgery is the mainstay of treatment for ganglioglioma. Surgical resection of the tumor is associated with good clinical and seizure outcome. Even if the seizure is not entirely cured by resection, the frequency of the seizures with decline significantly. Total resection is associated with higher rates of local control and survival, but it can be technically challenging due to the unclear border of the tumor. In cases of subtotal resection, adjuvant radiotherapy is helpful. If the resection fails to cure, adjuvant therapy with mTOR inhibitors could be considered. [1]
References
- ↑ Hayat, M. A. (2012). Tumors of the central nervous system. Dordrecht New York: Springer. ISBN 978-94-007-5487-4.