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Adult primary brain tumors are classified based on their origin, histology, and clinical behavior. The following is a breakdown of common primary brain tumors in adults, including descriptions, histological features, and clinical characteristics.
Tumor Type | Origin | Location | Clinical Features | Histological Features |
---|---|---|---|---|
Glioblastoma | Astrocyte | Cerebral hemispheres | Poor prognosis, median survival ~1 year | GFAP+, pseudopalisading cells, necrosis, hemorrhage |
Oligodendroglioma | Oligodendrocyte | Frontal lobes | Slow-growing, often calcified | Fried egg cells, chicken-wire capillary pattern |
Meningioma | Arachnoid cells | Near brain surfaces, parasagittal region | Seizures, focal neurologic signs | Whorled pattern, psammoma bodies |
Hemangioblastoma | Blood vessels | Cerebellum | Secondary polycythemia, associated with von Hippel-Lindau syndrome | Thin-walled capillaries, minimal intervening parenchyma |
Pituitary Adenoma | Endocrine cells | Pituitary gland | Visual disturbances (bitemporal hemianopia), prolactinoma symptoms | Hyperplasia of pituitary cells, prolactin, GH, ACTH |
Schwannoma | Schwann cells | Cerebellopontine angle, CN VIII | Hearing loss, tinnitus, NF-2 association | Biphasic pattern, S-100+ |