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| Oligodendroglioma |
| Etiology The etiology of the oligodendroglioma is unknown but most tumors show abnormalties of chromosome 19 and 1. |
| Pathogenesis See Etiology., |
| Epidemiology Oligodendrogliomas make up about 5% of intracranial tumors and 10% of gliomas. They are relatively slow growing except for the anaplastic variety which is rare. |
| General Gross Description Oligodendrogliomas are grey gelatinous masses in the brain that act as mass lesions. They are more comman in the cerebral hemispheres. |
| General Microscopic Description The tumor is made up of uniform oval cells with clear to pale pink cytoplasm and relatively uniform oval to round nuclei that have a fried egg or "box like" appearance. The stroma is made up of capillaries having a chickenwire appearance between groups of tumor cells. There is no good grading system and no specific immunoperoxidase stain to identify them. |
| Clinical Correlation Oligodendrogliomas act as mass lesions, infiltrating areas of brain. If they infiltrate the motor area, there are seizures of a focal motor type or hemiparesis. Infiltrating sensory regions may produce sensory symptoms or misinterpretations. They also are associated with edema so can produce herniation. |
| References Cotran RS, Kumar V, Robbins SL: Robbins Pathologic Basis of Disease. 5th ed. Philadelphia, W.B. Saunders, 1994, pp. 1343-1345. Poirer J et.al. Manual of basic neuropathology. Philadelphia: Saunders, 1990, pp.26-27. |
| Oligodendroglioma |
| Synopsis by: Dr ML Grunnet (TX2000M94503)[493] |
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