Epithelioid inflammatory myofibroblastic sarcoma with VCL–ALK fusion of central nervous system: case report and brief review of the literature

Author(s):  
Shefali Chopra ◽  
Nolan Maloney ◽  
Wei Lien Wang
Infection ◽  
1997 ◽  
Vol 25 (3) ◽  
pp. 171-174 ◽  
Author(s):  
Y.-T. Cheng ◽  
C.-T. Huang ◽  
H.-S. Leu ◽  
J.-S. Chen ◽  
M.-C. Kiu

2018 ◽  
Vol 10 (3) ◽  
pp. 338-341
Author(s):  
Christian Saleh ◽  
Nino Akhalbedashvili ◽  
Maria  Garcia Peraza ◽  
Konstantinos Athanasios Boviatsis ◽  
Margret  Hund-Georgiadis

Hemangioblastomas represent 3% of all central nervous system (CNS) tumors. The majority of CNS hemangioblastomas are infratentorial, with the cerebellum being the most frequent location, while 13% are found in the brainstem. Symptoms of brainstem hemangioblastomas can be very subtle and might therefore be overlooked or misinterpreted. We report the case of a patient with a hemangioblastoma at the junction of the medulla oblongata and the cervical spine and provide a brief review of the literature.


Neurosurgery ◽  
1986 ◽  
Vol 19 (6) ◽  
pp. 1016-1020 ◽  
Author(s):  
Walter A. Hall ◽  
Eduardo J. Yunis ◽  
Leland A. Albright

Abstract A 6-month-old girl had a gradually increasing head circumference. A preoperative computed tomographic (CT) scan of the head revealed an enhancing calcified partially cystic right frontal mass that was removed through a right frontotemporal craniotomy. On microscopic examination, the tumor was composed of sheets of neurons in a glial background alternating with highly cellular anaplastic areas. The diagnosis of anaplastic ganglioglioma was made. The child has done well for the 20 months since the operation without any evidence of tumor recurrence on subsequent CT scans. Because of the immaturity of the child's developing central nervous system, we have elected not to initiate radiotherapy at this time. The pertinent literature regarding gangliogliomas is reviewed.


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