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| __NOTOC__ | | __NOTOC__ |
| {{CMG}}
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| {{Oligodendroglioma}} | | {{Oligodendroglioma}} |
| | {{CMG}}{{AE}}{{S.M.}}{{SR}} |
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| ==Overview== | | ==Overview== |
| | There is no established [[system]] for the [[Staging (pathology)|staging]] of [[oligodendroglioma]]. |
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| ==Staging== | | ==Staging== |
| ===Histopathological Grading===
| | There is no established [[system]] for the [[Staging (pathology)|staging]] of [[oligodendroglioma]]. |
| The histopathologic grading of oligodendrogliomas is controversial. Currently the most commonly used grading schema is based on year 2007 [[World Health Organization]] (WHO) guidelines. Oligodendrogliomas are generally dichotomized into grade II (low grade) and grade III (high grade) tumors. The designation of grade III oligodendroglioma (high grade) generally subsumes the previous diagnoses of anaplastic or malignant oligodendroglioma.
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| Unfortunately, the WHO guidelines include subjective criteria in differentiating grade II and grade III tumors including the appreciation of “significant” hypercellularity and pleomorphism in the higher grade lesion. In addition, the presence of low mitotic activity, vascular proliferation and necrosis, including pseudopallisading necrosis are insufficient by themselves to elevate the grade of these tumors. This leads to inevitable interobserver variability in diagnosis by pathologists. The ultimate responsibility for making treatment decisions and interpretation of these diagnoses lies with the oncologist in consultation with the patient and their family.
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| It has been proposed that [[World Health Organization|WHO]] guidelines should contain a category for grade IV oligodendrogliomas which essentially appear to be glial neoplasms with overwhelming features of [[glioblastoma multiforme]] (GBM) arising from known lower grade oligodendrogliomas or GBM with a significant proportion of oligodendroglial differentiation. The diagnostic ultility of this latter category is uncertain as these tumors may behave either like glioblastoma or grade III oligodendrogliomas. As such, this is an exceptionally unusual diagnosis.
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| The updated WHO guidelines published in 2007 recommends classifying such tumors for the time being as ‘glioblastoma with oligodendroglioma component’. <ref>{{cite journal |author=Louis D, Ohgaki H, Wiestler O, 'et al'' |title=The 2007 WHO Classification of Tumours of the Central Nervous System |journal=Acta Neuropathologica |volume=114 |issue=2 |pages=97-109 |year=2007 |pmid=17618441 |doi=10.1007/s00401-007-0243-4}}</ref> It remains to be established whether or not these tumors carry a better prognosis than standard glioblastomas.
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| ==References== | | ==References== |
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| [[Category:Types of cancer]] | | [[Category:Types of cancer]] |
| [[Category:Neurosurgery]] | | [[Category:Neurosurgery]] |
| [[Category:Oncology]]
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| [[Category:Disease]] | | [[Category:Disease]] |
| [[Category:Mature chapter]] | | [[Category:Mature chapter]] |
| [[Category:Needs content]] | | [[Category:Up-To-Date]] |
| | [[Category:Oncology]] |
| | [[Category:Medicine]] |
| | [[Category:Neurology]] |
| | [[Category:Neurosurgery]] |