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49 Cards in this Set
- Front
- Back
What's a tumor involving neurons and neuroglial cells?
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Ganglioneuroma
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Name the 4 Primitive neuroepithelial neoplasms
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Medulloblastoma
Pineoblastoma Ependymoblastoma Medulloepithelioma |
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What's the most common type of tumor you see in the brain?
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Metastatic
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Which of the 4 CNS malformative tumors mentioned happens in the young? What are the other 3?
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Young = Colloid Cyst
Craniopharyngioma Epidermoid cyst Dermoid cyst |
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What's biologic malignancy refer to?
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Histologically benign brain tumors may be fatal because their location precludes resection and the margins are not grossly visible
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2 major mechanisms of CNS tumor spread?
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Local extension
Intraneural seeding via meninges and ventricles |
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Do CNS tumors met outside the CNS?
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Only very rarely
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What are the factors that determine the clinical effect and prognosis of a CNS tumor?
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Growth rate (fast = bad)
Location (helps determine sx) Pt age (the older you are the worse it is) |
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Location, frequency and age group affected by fibrillary/diffuse astrocytomas?
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Common (most common glioma). Typically in the cerebral hemispheres (white matter) of adults.
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Gross appearance of fibrillary/diffuse astrocytomas?
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margins poorly defined
solid distort architecture |
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What's the grading system for astrocytomas?
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I-IV based on differentiation (IV is the worst)
Astrocytoma = I or II anaplastic astrocytoma = III glioblastoma multiforme = IV |
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Peak incidence and origin of glioblastoma multiforme?
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Peak incidence 40-60 years
May arise from dedifferentiating astrocytoma (or any glioma, really) or de novo |
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Gross appearance of a glioblastoma multiforme?
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cystic/solid (well demarcated), necrotic and hemorrhagic, found in the cerebral hemispheres (likes to cross corpus callosum)
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Micro appearance of a glioblastoma multiforme?
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dedifferentiated and cellular with palisading (picket fence) necrosis and microvascular proliferation (bad sign)
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Prognosis of a glioblastoma multiforme?
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Mean length of survival after diagnosis is 15 months
Only 25% alive after two years |
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Who gets pilocytic astrocytomas? Where do they appear?
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More common in children
common locations = Cerebellum (= mural nodule in a cyst), chiasm, hypothalamus |
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Prognosis of pilocytic astrocytomas?
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depends on resectability, usually better than fibrillary astrocytoma
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Micro appearance of pilocytic astrocytomas?
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“hairlike” cellular processes
not very cellular |
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Frequency of oligodendrogliomas? Where do they appear and who gets them?
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5-15% of gliomas
Adult Cerebral hemispheres |
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Prognosis of oligodendrogliomas?
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Average survival 5-10 years (not really correlated with histology)
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What's an oligodendroglioma that's associated with an astrocytoma called?
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oligoastrocytoma
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What feature helps improve the prognosis of an oligodendroglioma?
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1p/19q deletion tumors respond well to treatment and have a better prognosis, irrespective of histology
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Gross appearance and behavior of an oligodendroglioma?
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Calcification frequent
Many are very slow growing - Survival doesn't correlate as well with histology as astrocytomas |
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Where do ependymomas appear and who gets each type?
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Brain (4th ventricle)- pt usually under 20 years
Spinal cord - adults |
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Incidence of ependymomas?
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Uncommon (5-10% of gliomas)
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Morphology and behavior of ependymomas in the brain?
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Arise from ependymal lining of the 4th ventricle Solid or papillary
Dangerous due to proximity to vital brainstem nuclei and propensity to spread through CSF |
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Micro appearance of ependymomas?
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rosettes (malignant epidenymal cells line around white matter/neural processes) and pseudorosettes (cells lining blood vessels)
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Morphology of ependymomas in the spinal cord?
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Myxopapillary, arising from filum terminale
May be well demarcated from normal tissue |
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Prognosis of ependymomas in the spinal cord?
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depends on completeness of resection
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Signs/symptoms of ependymomas based on location?
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Fourth ventricle: hydrocephalus sxs
Cauda equina: radicular pain, sensory loss, motor weakness or paralysis, fasciculations |
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Prognosis of ependymomas in the brain?
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50-70% 5 yr survival - depends on CSF dissemination and resection completeness
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Incidence of Choroid plexus papillomas? Who gets them and where?
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Uncommon
More frequent in children (typically in lateral ventricles) Less frequent in adults (typically 4th ventricle) |
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Morphology and behavior of Choroid plexus papillomas?
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Morphologically similar to normal choroid
Produce CSF—can cause hydrocephalus |
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Who gets colloid cysts of the third ventricle?
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Young adults
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Clinical presentation of colloid cysts of the third ventricle?
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Clinical: headaches, coma, death
(if it obstructs the foramina of Munro) |
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Gross morphology of colloid cysts of the third ventricle?
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thin walled cyst with gelatinous material
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Who gets medulloblastomas? Where do they occur?
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Pts < 20 y/o
Mostly in the cerebellar vermis |
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What's the prognosis of medulloblastomas?
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Highly malignant but responds well to tx
5 year survival = 75% |
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Symptoms of medulloblastomas?
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Symptoms of increased CSF pressure and cerebellar damage
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Gross morphology of medulloblastomas?
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Small cell tumor
Gross: fleshy |
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Micro appearance of medulloblastomas?
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Very cellular and undifferentiated with Homer Wright rosettes (look like poorly differentiated ependyomas)
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Who gets primary CNS lymphomas? Behavior of this neoplasm?
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AIDs defining condition.
Usually B cell with angiocentric growth (grows along blood vessels). Same classifications as peripheral |
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What's a meningioma? Where do they occur?
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Benign tumor of meninges arising from meningothelial cell
Common in dorsolateral convexities, olfactory region, or foramen magnum |
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Incidence of meningiomas? Who gets them? Do they normally come in multiples?
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Very common - usually in adults
Inc incidence in females due to progesterone receptors Solitary except in patients with neurofibromatosis |
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Signs/sx of meningiomas?
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Generalized or local signs
(can be undetected for years depending on loction) |
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Prognosis of meningiomas?
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Prognosis depends on surgical accessibility, location, microscopic appearance - Usually do well but can recur
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Morphology of meningiomas?
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Well demarcated, Firm
Attached to dura anywhere in CNS |
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Where do most mets to the CNS come from?
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80% from: lung, breast, melanoma, kidney, GI
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Where do CNS mets usually go? What's a common complication?
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Can be parenchyma or meninges
Frequently multiples = can cause considerable surrounding edema |