-
Journal of neurosurgery · Jul 2003
Review Case ReportsMagnetic resonance imaging of intramedullary spinal cord schwannomas. Report of two cases and review of the literature.
- Cesare Colosimo, Alfonso Cerase, Luca Denaro, Giulio Maira, and Romano Greco.
- Department of Clinical Sciences and Bioimaging, Neuroradiology Section, Institute of Advanced Biomedical Technology, "Gabriele d'Annunzio" University of Chieti, School of Medicine, Chieti, Scalo, Italy. colosimo@radiol.unich.it
- J. Neurosurg. 2003 Jul 1; 99 (1 Suppl): 114-7.
AbstractIntramedullary spinal cord schwannomas are rare benign tumors for which resection is possible and safe. The purpose of this paper is to present the magnetic resonance (MR) imaging features in two cases of intramedullary spinal cord schwannoma to assist both neurosurgeons and pathologists in preventing misdiagnosis and resultant partial resection. The MR imaging evidence of a small- or medium-sized well-marginated intramedullary spinal cord tumor in a patient in whom no syringomyelia is present but in whom moderate edema with marked Gd enhancement can be seen shouldbe considered in the differential diagnosis of intramedullary spinal cord schwannoma. In cases in which an associated thickened Gd-enhancing spinal nerve root is seen the diagnosis of schwannoma should be assumed.
Notes
Knowledge, pearl, summary or comment to share?You can also include formatting, links, images and footnotes in your notes
- Simple formatting can be added to notes, such as
*italics*
,_underline_
or**bold**
. - Superscript can be denoted by
<sup>text</sup>
and subscript<sub>text</sub>
. - Numbered or bulleted lists can be created using either numbered lines
1. 2. 3.
, hyphens-
or asterisks*
. - Links can be included with:
[my link to pubmed](http://pubmed.com)
- Images can be included with:
![alt text](https://bestmedicaljournal.com/study_graph.jpg "Image Title Text")
- For footnotes use
[^1](This is a footnote.)
inline. - Or use an inline reference
[^1]
to refer to a longer footnote elseweher in the document[^1]: This is a long footnote.
.