scholarly journals Posterior fossa brain metastasis from primary osteogenic sarcoma: A rare entity

2016 ◽  
Vol 2 (2) ◽  
pp. 28
Author(s):  
M. S. Ahmed ◽  
S. Imtiaz ◽  
A. Hamid ◽  
M. K. Shazlee
2000 ◽  
Vol 8 (6) ◽  
pp. 1-4 ◽  
Author(s):  
Narendra N. Datta ◽  
Kwong Y. Chan ◽  
John C. K. Kwok ◽  
Christopher Y. F. Poon

Patients with cerebellar arteriovenous malformations (AVM) commonly present to the neurosurgical department after having suffered hemorrhages. The subarachnoid space is the usual location for these often repeating episodes of bleedings. In addition, these patients can present with parenchymal hemorrhage. Acute subdural hematoma caused by a ruptured cerebellar AVM is a rare entity and is not generally recognized. The authors present a case of acute posterior fossa subdural hematoma resulting from a ruptured cerebellar AVM.


1971 ◽  
Vol 35 (6) ◽  
pp. 672-676 ◽  
Author(s):  
A. Loren Amacher ◽  
Larry K. Page

✓ Four patients with hydrocephalus due to membranous obstruction of the fourth ventricle are presented. This rare entity produced radiographic and clinical findings suggestive of posterior fossa tumor. Operative findings included normal cerebellar development and a translucent membrane just above the foramen of Magendie. Etiological possibilities are discussed.


2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Jordan Nepute ◽  
Jinping Lai ◽  
Yihua Zhou

Intracranial capillary hemangioma (ICH) is a rare entity, with approximately 24 reported cases in the literature. There are only three reported cases of ICH in an adult male. In this case report, we describe the fourth documented case of ICH in an adult male and, to the best of our knowledge, the first ever documented case of ICH in the posterior fossa of an adult male. We also discuss its imaging appearance and differential diagnosis.


2006 ◽  
Vol 8 (2) ◽  
pp. 75-77
Author(s):  
Ashok K. Vaid ◽  
Komal Bhatia ◽  
Vineet Talwar ◽  
Dinesh C. Doval ◽  
Sudhir Rawal ◽  
...  

2013 ◽  
Vol 27 (4) ◽  
pp. 519-520 ◽  
Author(s):  
J. L. Vitorino-Araujo ◽  
J. C. E. Veiga ◽  
V. R. Barboza ◽  
N. de Souza ◽  
D. Mayrink ◽  
...  

2014 ◽  
Vol 21 (5) ◽  
pp. 769-772 ◽  
Author(s):  
Kelly B. Mahaney ◽  
Arnold H. Menezes

An intradiploic CSF pseudocyst is a rare entity that has been described in association with trauma, as a sequela of untreated hydrocephalus, or occasionally as a congenital finding in older adults. The authors present the case of a woman with a remote history of a posterior fossa intradural procedure, in which she underwent Chiari malformation decompression, Silastic substitute–assisted duraplasty, and occipitocervical fusion; she presented 19 years later with recurrent symptoms of Chiari malformation. She was found to have an occipital intradiploic pseudomeningocele, arising within her dorsal occipitocervical fusion mass and resulting in dorsal hindbrain compression. She underwent a posterior fossa decompression and revision of her failed duraplasty, and she had a good recovery. This case demonstrates intradiploic CSF pseudomeningocele as a rare potential delayed complication of an intradural procedure for the treatment of Chiari malformation with occipitocervical fusion.


2008 ◽  
Vol 51 (1) ◽  
pp. 56 ◽  
Author(s):  
V Maheshwari ◽  
AS Farhan ◽  
KAlam Adreena

2011 ◽  
Vol 59 (4) ◽  
pp. 639 ◽  
Author(s):  
AmitN. D Dwivedi ◽  
Kumkum Gupta ◽  
PrashantK Gupta ◽  
Gouri Garg

2013 ◽  
Vol 108 ◽  
pp. S185
Author(s):  
Ibrahim Abdullah ◽  
Sarah Arnold ◽  
Ayad Alkhatib ◽  
Waqas Qureshi ◽  
Syed Hassan

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