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65 Cards in this Set
- Front
- Back
Most common form of primary brain cancer.
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meningioma
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Most common primary tumor in children
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Medulloblastoma
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Which population are menigiomas more common?
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women and older populations
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Meningiomas are commonly seen in this genetic disease.
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NF-2
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Menigiomas arise from which cells?
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arachnoid cap cells
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Histiologic appearance of meningiomas.
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whorls of tightly packed cells around calcified acellular material called psammoma bodies
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Primitive neuroectodermal tumors (PNETs) usually arise ?
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posterior fossa
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Medulloblastoma can metastasize to ?
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bone
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Symptoms of PNETs?
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related to mass effect in posterior fossa: ataxia, balance and equilibrium disturbances, cranial nerve palsies
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Which pathway may be involved in the development of medulloblastomas?
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Sonic Hedgehog
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Histological appearance of medulloblastoma.
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prominent nuclei w/ little cytoplasm; very uniform sheets of cells
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Oligodendrogliomas are often ___ and patients often present with ___.
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calcified, seizures
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Oligodendrogliomas are more ____ based as opposed to astrocytomas which are ____.
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cortically, deeper
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Histology of oligodendrogliomas.
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"fried egg" appearance, very fine vascular pattern described as a chicken wire appearance
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Loss of what parts of chromosomes is associated w/ oligodendrogliomas and portends a favorable prognosis.
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1p and 19q
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The majority of primary CNS lymphomas fall into the ____ category
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large B cell
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Treatment of CNS lymphoma:
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methotrexate to inhibit dihydrofolate reductase; leukovorin rescues purine synthesis pathway in the rest of the body
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Which CNS neoplasm is the most malignant?
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Astrocytoma (type IV, GBM)
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Histologically the main difference between grade III and grade IV astrocytomas.
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necrosis and neovascularizaiton
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If this gene is silenced by methylation then a patient will respond better to treatment with temozolomide.
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MGMT
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De novo GBM is associated with amplification of ___ and loss of ___.
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EGFR, PTEN
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Intermediate filament found in the cytoplasm of normal astrocytes, reactive astrocytes, and astrocytic tumors.
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GFAP
"Good For Astrocyte Peeking" |
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Grade II and III frequently have a mutation in ___.
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p53
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Viable tumor cells around necrosis; seen in GBM.
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pseudopallisading necrosis
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Better prognosis: Secondary or Primary GBM?
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Secondary, but still poor
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Mutations in Secondary GBM
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p53 & Rb loss
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Mutations in Primary GBM
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EGFR amplification, p16 deletion, PTEN deletion
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Typical histological finding in ependymal tumors
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rosettes around blood vessels
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Defective oncogene seen in sporadic menigiomas.
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merlin from monosomy of chromosome 22
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Histological appearance of CNS lymphoma.
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Angiocentric pattern, with lymphocytes expanding hte Virchow-Robin space
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Most common CNS tumor in children.
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Piliocytic Astrocytoma
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Acellular eosinophilic material with a glassy appearance often found in pilocytic astrocytomas.
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Rosenthal fibers
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Tumor cells surround acellular material, seen in medulloblastomas.
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Homer-Wright rosettes
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Benign tumors found in the sella turcica, compress the pituitary and optic chiasm.
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Craniopharyngiomas
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Histology of craniopharyngiomas.
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Multiple cysts. Tumor cells show evidence of squamous differentiation w/ keratin formation.
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PNS, numerous Schwannomas and subcutaneous neurofibrommas.
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NF-1 (Von Recklinhausen's disease)
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NF-1 inheritence.
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Autosommal dominant
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NF-1 is due to ______/
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Deletion of gene on chromosome 17 for protein that inactvates Ras.
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Difference between neurofibroma and Schwannoma.
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Schwannoma only involves some of the nerve rootlets. Neurofibroma is more invasive and whole nerve will be sacrificed.
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CNS, bilateral acoustic Schwannomas, increased incidence of astrocytomas and meningiomas.
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NF-2
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NF-2 caused by deletion of gene ____.
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merlin on chromosome 22.
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Visceral schwannomas and neurofibromas and of adrenal gland.
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NF-3
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Inheritence of NF-2
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Autosommal dominant.
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Histology of schwannoma.
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Elongated nuclei, stack on top of each other forming Antoni type A or Verocay bodies.
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Two genes involved in tuberous sclerosis:
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TSC-1 on chromosome 9 (hamartin) and TSC-2 found on chromosome 16 (tuberin)
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Inheritence of tuberous sclerosis:
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AD
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Lesions seen in Tuberous Sclerosis:
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glial hamartomas, subpendymal giant cell astrocytomas
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Common location of schwannomas.
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cerebellar pontine angle involving CN VIII
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Common clinical presentation of an astrocytoma.
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headache
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Two tumors from neural CREST origin.
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menigiomas and schwannomas
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Where are more pediatric brain tumors distributed compared to adult brain tumors?
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posterior fossa
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What is the importance of doing a T1 MRI WITH CONTRAST?
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contrast can get to areas where the BBB has been breeched (e.g. a tumor!)
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Imaging of low grade astrocytoma.
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CT- low density, non enhancing
MRI - iso/hypointense on T1, hyperintense on T2 PET - hypometabolic |
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Imaging of Grade III astrocytoma.
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CT - frequent mass effect
MRI - inhomogeneity, T2 diffuse area of edema PET - hypermetabolic |
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Imaging of GBM.
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CT & MRI - inhomogenous T2 hyperintense, hetergeneously enhancing b/c of necrosis
PET - hypermetabolic |
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Imaging of meningioma.
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CT - iso/hypointense, homogenous, can be calcified
MRI - iso/hypointense on T1, variable on T2 |
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Imaging of metastases.
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CT - discrete and noninfiltrative, edema
MRI - low attenuation on T1, little attenuation on T2, often cystic or necrotic center PET - hypermetabolic |
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Imaging of medulloblastoma.
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CT - iso/hypointense w/ edema, homogenous
MRI - hypointense on T1, variable on T2, 4th ventricular extension |
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Positive prognostic factors for higher grade astrocytomas.
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Grade III better than IV.
Younger patients do better. Healthier patients do better |
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Whole brain radiotherapy is appropriate in patients with greater than ____ metastatic lesions.
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3
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Gold standard to determine between a tumor and radiation necrosis.
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resection/biopsy
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What is used to prevent seizures during interoperative mapping?
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iced ringers lactate
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Balloon filled with radioactive liquid placed in the brain.
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Brachytherapy
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Gamma knife is most often used for which tumors?
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metastatic brain tumors
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Which cancer has the highest propensity to metastasize to the brain?
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Melanoma
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