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Highest incidence age is 3–12 y and 55–65 y.
Account for 80% of adult CNS tumors; incidence of primary tumor is ∼15–20:100,000 per y.
Account for one-third of childhood CNS tumors.
Increased ICP: Headache, seizures, neurologic deficit/dementia, visual and hearing changes, focal neurologic changes (hemiparesis, numbness, ataxia), and/or visual deficits if pituitary tumor present
Endocrinopathy, fluid, and electrolyte imbalance
AEDs: Dilantin, keppra, tegretol. Adequate levels needed to avoid postop seizures.
Raised ICP and brain edema: May lead to herniation (transtentorial [dilate ipsilateral] pupil), subfalcine (leg weakness), tonsillar (neck stiffness, spasticity, extensor-plantar response), and upward transtentorial (small pupils, extensor rigidity).
Dexamethasone Rx may lead to hyperglycemia.
Hyperglycemia may cause more retractor-induced ischemic injury to adjacent brain tissues.
Endocrinopathy, particularly diabetes insipidus, if near pituitary.
Portion of brain superior to tentorium cerebella.
13,000 deaths per y; third leading cause of death in pts 15–34 y of age.
Brain edema surrounding malignant tumors causes initial Sx; often improve initially after corticosteroids.
Seizures due to local neuronal irritation; 30–70% incidence related to tumor type.
Obstructive hydrocephalus if the tumor is near third ventricle or foramen of Monro.
In adults, 85% of primary tumors occur in anterior two-thirds of cortex (most benign): glioma (45–50%), medulloblastoma, ependymoma, low-grade lymphoma (children: astrocytoma, medulloblastoma). 15% are meningiomas. Common presentation age is 55–65 y (1% of all cancers).
Many supratentorial tumors are metastases (20–30%): Melanoma, breast cancer, small-cell lung, non-Hodgkin’s lymphoma, colon, renal, nasal/throat. 50% have multiple metastases (25% of all pts with cancer have brain metastases), usually located at white-gray border.
Associated Dx includes neurofibromatosis and von Hippel-Lindau syndrome.
Brain tumors rarely metastasize outside the brain.
Pediatric (uncommon >age 2) <1 y present when large (pliable skull, glioma 50%; (astrocytoma). Most are low-grade and deep midline; others are ependymoma, medulloblastoma, and PNET (primitive neuroectodermal tumors).
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