Ependymoma surgery: Difference between revisions
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*Complete surgical removal is often curative. Some subependymomas are considered incidental findings and observed without intervention. | *Complete surgical removal is often curative. Some subependymomas are considered incidental findings and observed without intervention. | ||
*Extensive surgical resection in attempt to maximal tumor reduction | *Extensive surgical resection for anaplastic ependymoma ([[WHO]] grade III) in attempt to maximal tumor reduction is related to improved survival rate.<ref name="pmid827-35">{{cite journal| author=Tennyson VM, Mytilineou C, Heikkila R, Barrett RE, Cohen G, Côté L et al.| title=Dopamine-containing neurons of the substantia nigra and their terminals in the neostriatum. | journal=UCLA Forum Med Sci | year= 1975 | volume= | issue= 18 | pages= 227-64 | pmid=827-35 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=827 }} </ref><ref name="pmid258-66">{{cite journal| author=Zourlas PA| title=Response to exogenous gonadotropins in the unresponsive ovary syndrome. | journal=Int J Gynaecol Obstet | year= 1975 | volume= 13 | issue= 1 | pages= 23-8 | pmid=258-66 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=258 }} </ref> | ||
==References== | ==References== |
Revision as of 18:08, 8 October 2015
Ependymoma Microchapters |
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Ependymoma surgery On the Web |
American Roentgen Ray Society Images of Ependymoma surgery |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Surgery is the main stay of treatment for myxopapillary ependymoma (WHO grade 1), myxopapillary ependymoma (WHO grade 1), ependymoma (WHO grade I), and anaplastic ependymoma (WHO grade III).
Surgery
- Anecdotal experience suggests that surgery alone for completely resected supratentorial nonanaplastic tumors and intradural spinal cord ependymomas may be an appropriate approach to treatment for:[1]
- Newly diagnosed myxopapillary ependymoma (WHO grade 1)
- Newly diagnosed myxopapillary ependymoma (WHO grade 1)
- Newly diagnosed ependymoma (WHO grade I)
- Newly diagnosed anaplastic ependymoma (WHO grade III)
- Complete surgical removal is often curative. Some subependymomas are considered incidental findings and observed without intervention.
- Extensive surgical resection for anaplastic ependymoma (WHO grade III) in attempt to maximal tumor reduction is related to improved survival rate.[2][3]
References
- ↑ Ependymoma http://www.cancer.gov/types/brain/hp/child-ependymoma-treatment-pdq/#cit/section_7.1 URL Accessed on 10 8 2015
- ↑ Tennyson VM, Mytilineou C, Heikkila R, Barrett RE, Cohen G, Côté L; et al. (1975). "Dopamine-containing neurons of the substantia nigra and their terminals in the neostriatum". UCLA Forum Med Sci (18): 227–64. PMID 827-35 Check
|pmid=
value (help). - ↑ Zourlas PA (1975). "Response to exogenous gonadotropins in the unresponsive ovary syndrome". Int J Gynaecol Obstet. 13 (1): 23–8. PMID 258-66 Check
|pmid=
value (help).