Bilateral thalamic glioma - case report and review

Author(s):  
Adrian-florian Balasa ◽  
Rodica-ioana Balasa ◽  
Imre Zsigmund Egyed ◽  
Rares Chinezu
2000 ◽  
Vol 42 (10) ◽  
pp. 732-734 ◽  
Author(s):  
H. Hirano ◽  
S. Yokoyama ◽  
M. Nakayama ◽  
S. Nagata ◽  
J. Kuratsu

2019 ◽  
Vol 18 ◽  
pp. 100499
Author(s):  
O.A. Badejo ◽  
B.E. Osobu ◽  
A.A. Salami ◽  
A.O. Adeyinka ◽  
M.T. Shokunbi

2002 ◽  
Vol 42 (10) ◽  
pp. 443-446 ◽  
Author(s):  
Masafumi UCHINO ◽  
Satoru KITAJIMA ◽  
Chikao MIYAZAKI ◽  
Iekado SHIBATA ◽  
Myouta MIURA

2016 ◽  
Vol 181 (9-10) ◽  
pp. 723-733 ◽  
Author(s):  
Maddalena Chermetz ◽  
Margherita Gobbo ◽  
Katia Rupel ◽  
Giulia Ottaviani ◽  
Giancarlo Tirelli ◽  
...  

2011 ◽  
Vol 28 (2) ◽  
pp. 327-330 ◽  
Author(s):  
Jason D. Hill ◽  
Michael S. Rhee ◽  
John R. Edwards ◽  
Matthew C. Hagen ◽  
Daniel H. Fulkerson

2019 ◽  
Vol 38 (01) ◽  
pp. 047-050
Author(s):  
Gonçalo Figueiredo ◽  
Sérgio Moreira ◽  
Célia Pinheiro ◽  
Alfredo Calheiros

AbstractAnaplastic oligodendrogliomas (AOs) correspond to ∼ 23% of all oligodendrogliomas. They correspond to a tumor with malignant histological characteristics, focal or diffuse, associated with a worse prognosis. In the present case report, we describe the case of a 30-year-old female submitted to resection of a right parietal lesion whose histology showed to be an AO. She underwent complementary treatment with chemotherapy and radiotherapy according to the Roger Stupp protocol. Four years after the initial diagnosis, there was tumor recurrence within the superior sagittal sinus, with no evidence of recurrence elsewhere. In the literature, we have found no similar published case reinforcing the rarity of this condition


Neurosurgery ◽  
1983 ◽  
Vol 13 (6) ◽  
pp. 692-694
Author(s):  
Nancy E. Epstein ◽  
Alan D. Rosenthal ◽  
Jay Selman ◽  
Michael Osipoff ◽  
Roger A. Hyman

Abstract Intracranial gliomas are found in association with von Recklinghausen's neurofibromatosis. However, few truly neonatal lesions have been identified and studied. This case report concerns a 4-month-old child who was found to have a massive thalamic glioma of moderate grade. Four paternal generations had suffered from different manifestations of this transmissible autosomal-dominant (Ad) phakomatosis.


2015 ◽  
Vol 7 ◽  
pp. 168-171 ◽  
Author(s):  
Barbara A. Morais ◽  
Djalma F.S. Menendez ◽  
Raphael S.S. Medeiros ◽  
Manoel J. Teixeira ◽  
Guilherme A. Lepski

2014 ◽  
Vol 16 (suppl 2) ◽  
pp. ii105-ii105
Author(s):  
F. Romeo ◽  
G. Maddalena ◽  
V. Conserva ◽  
V. Fumai ◽  
L. Fiorentino ◽  
...  

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