Hostname: page-component-76fb5796d-skm99 Total loading time: 0 Render date: 2024-04-25T11:49:17.618Z Has data issue: false hasContentIssue false
  • English
  • Français

Chondrosarcoma of the Skull Base in Ollier's Disease

Published online by Cambridge University Press:  23 September 2014

Naif M. Alotaibi ,
Alireza Mansouri ,
Felipe G. Carvalho ,
James A. Balogun  and
Fred Gentili
Naif M. Alotaibi
Affiliation:
Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario, Canada Department of Neurosurgery, National Neuroscience Institute(NNI), King Fahad Medical City, Saudi Arabia
Alireza Mansouri*
Affiliation:
Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario, Canada
Felipe G. Carvalho
Affiliation:
Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario, Canada
James A. Balogun
Affiliation:
Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario, Canada Federal Medical Center Owo, Ondo State, Nigeria
Fred Gentili
Affiliation:
Division of Neurosurgery, Department of Surgery, University of Toronto, Ontario, Canada
*
Division of Neurosurgery, Department of Surgery, University of Toronto, 399 Bathurst St., WW 4-427 Toronto, Ontario, M5T 2S8, Canada. Email: alireza.mansouri@utoronto.ca.
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Neuroimaging Highlight
Information
Canadian Journal of Neurological Sciences , Volume 41 , Issue 1 , January 2014 , pp. 86 - 87
Copyright
Copyright © The Canadian Journal of Neurological 2014

References

1. Halal, F, Azouz, EM. Generalized enchondromatosis in a boy with only platyspondyly in the father. Am J Med Genet. 1991;38:588–92.Google Scholar
2. Silve, C, Juppner, H. Ollier disease. Orphanet J Rare Dis. 2006;1:37.Google Scholar
3. D’Angelo, L, Massimi, L, Narducci, A, Di Rocco, C. Ollier disease. Childs Nerv Syst. 2009;25:647–53.Google Scholar
4. Amary, MF, Damato, S, Halai, D, et al. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nat Genet. 2011;43:1262–5.Google Scholar
5. Sarwar, M, Swischuk, LE, Schecter, MM. Intracranial chondromas. AJR Am J Roentgenol. 1976;127:973–7.CrossRefGoogle ScholarPubMed
6. Duan, F, Qiu, S, Jiang, J, et al. Characteristic CT and MRI findings of intracranial chondroma. Acta Radiol. 2012;53:1146–54.Google Scholar