A rare brain tumour that develops from cells which make up the supporting connective tissue around brain nerve cells. Symptoms will depend on which area of the brain the tumor is present in. Oligodendrogliomas are more common in adults than children and more common in males than females. There is no known cause of the tumors. ...more »
Symptoms of Oligodendroglioma
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symptoms of Oligodendroglioma
Treatments for Oligodendroglioma
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Home Diagnostic Testing
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Wrongly Diagnosed with Oligodendroglioma?
Oligodendroglioma: Related Patient Stories
Diagnostic Tests for Oligodendroglioma
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Causes of Oligodendroglioma
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Disease Topics Related To Oligodendroglioma
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Oligodendroglioma: Undiagnosed Conditions
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Misdiagnosis and Oligodendroglioma
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because he suffered from sudden...read more »
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Oligodendroglioma: Rare Types
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Research about Oligodendroglioma
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Clinical Trials for Oligodendroglioma
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and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Oligodendroglioma include:
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Clinical Trials for Oligodendroglioma
Statistics for Oligodendroglioma
Oligodendroglioma: Broader Related Topics
Types of Oligodendroglioma
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Definitions of Oligodendroglioma:
Oligodendroglioma is a well-differentiated (WHO grade II), diffusely infiltrating tumor of adults, typically located in the cerebral hemispheres and composed predominantly of cells which morphologically resemble oligodendroglia. They are moderately cellular and composed of tumor cells with rounded, homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). Oligodendrogliomas generally recur locally, with median post-operative survival times ranging from 3 to 5 years for patients with all histological grades. (Adapted from WHO.)
- (Source - Diseases Database)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Oligodendroglioma as a "rare disease".
Source - Orphanet
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