scholarly journals P10.10 Pleomorphic xanthoastrocytoma without a tumor mass lesion influences intracranial hemorrhage: case report

2017 ◽  
Vol 19 (suppl_3) ◽  
pp. iii87-iii87
Author(s):  
Y. Hanashima ◽  
T. Ohta ◽  
Y. Takamine ◽  
A. Yoshino
2014 ◽  
Vol 30 (1) ◽  
pp. 213-216
Author(s):  
Tomoya Hasegawa ◽  
Junya Kojima ◽  
Reiko Zaitu ◽  
Kazunori Mukaida ◽  
Rina Kato ◽  
...  

2019 ◽  
Vol 6 (1) ◽  
pp. 39-42
Author(s):  
Yusuke Takamine ◽  
Shun Yamamuro ◽  
Koichiro Sumi ◽  
Takashi Ohta ◽  
Katsunori Shijo ◽  
...  

Pulse ◽  
2017 ◽  
Vol 9 (1) ◽  
pp. 45-48
Author(s):  
MR Molla ◽  
F Ferdousi ◽  
DR Shankar ◽  
AKMB Karim

A 13 years old boy admitted with the complaint of progressive exophthalmos and gradually decreasing vision on right eye, also occasional headache and deformity on the right fronto-orbital region. Radiological & clinical findings revealed a case of frontal osteoma in the right frontal sinus extending up to right frontal lobe, eroding right roof of the orbit. Complete excision of the tumor mass was possible surgically. Biopsy confirmed a case of osteoma. Below is a discussion on diagnosis & management of frontal osteomaPulse Vol.9 January-December 2016 p.45-48


2010 ◽  
Vol 283 (S1) ◽  
pp. 19-22 ◽  
Author(s):  
Jun Kakogawa ◽  
Miyuki Sadatsuki ◽  
Norio Masuya ◽  
Hideto Gomibuchi ◽  
Hiroyasu Ohno ◽  
...  

2019 ◽  
Vol 10 ◽  
pp. 250 ◽  
Author(s):  
Sukwoo Hong ◽  
Takayuki Hara

Background: In neurosurgical practice, we rarely encounter hybrid nerve sheath tumors (HNST) in the orbit. We recently had a patient of this rare tumor. We believe that this is the first report where we resected the tumor transcranially. Case Description: A 54-year-old male presented with the left proptosis and intraconal tumor of 43 mm. We performed fronto-orbital craniotomy to resect the tumor mass. His proptosis completely improved and discharged home with a modified Rankin Scale of 1. Conclusion: Transcranial resection of orbital HNST was a safe and effective way to treat. Since we do not have much data regarding this rare tumor, we need to accumulate more cases.


Author(s):  
Ricardo Menèndez ◽  
Julio Fernàndez ◽  
Alfredo Monti ◽  
Gustavo Sevlever

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