11-05 Nervous System Tumors Flashcards

1
Q

1 most important prognostic feature in CNS tumors

A

tumor’s “grade” as determined by Path

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2
Q

define the different grades of CNS tumors

A
I – benign, unlikely to recur or spread
II – slow growing, but will come back
III – aggressive, requires therapy more
than surgery alone
IV – anaplastic, malignant, lethal
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3
Q

most common intracranial tumor

A

meningioma

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4
Q

germ cell tumors

A

any tumor that can occur in testes or ovaries can occur in CNS as a 1° tumor!

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5
Q

consequences of brain hernations

A

—Necrosis of that area
—infarction b/c blood supply compressed
—nerve compression (esp CNs)
—death due to b.s. compression in tonsillar hernia

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6
Q

When CN III is compressed what f(x) 1st affected?

A

para-sympathetics are on the outside so blown pupils?

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7
Q

What syndrome is associated with CN VIII Schwannoma?

A

NF2

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8
Q

What syndrome is associated with Cerebellar Gangliocytoma?

A

Cowden’s syndrome (tumors in many different systems)

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9
Q

What syndrome is associated with Cerebellar Hemangioblastoma?

A
von Hippel-Lindau syndrome: a rare, autosomal dominant genetic condition that predisposes individuals to benign and malignant tumours most commonly: 
—CNS and retinal hemangioblastomas
—clear cell renal carcinomas
—pheo
—pancreatic neuroendocrine
—pancreatic cysts
—endolymphatic sac tumors
—epididymal papillary cystadenomas
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10
Q

Astrocytomas 101

A

—Some low-grade, some high-grade
—Astrocytes = cell type of the tumor
—Diffuse, infiltrative tumor boundry; No surgical border (true of all glial tumors)
—“Naked nuclei” (large irreg nuc; cell has seemingly no cytoplasm)
—production of GFAP (glial fibrillary acidic protein)

Gradient of WHO Grades of Astrocytomas:
—Grade I: Pilocytic (“thread-like”) type (w/ “Rosenthal material” = fibers) are usually very low-grade and are common in KIDS
—Grade IV: GBM (see sep slide)

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11
Q

Glioblastoma Multiforme Astrocytoma 101

A

AS WITH ALL ASTROCYTOMAS:
—Naked nuclei
—No tumor boundries

UNIQUELY:
—Necrosis with pseudopallisading
—Endothelial proliferation
—Highly anaplastic (wild, wild cell types)
—Diffuse brain infiltration

WHO GRADE IV =(

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12
Q

Oligodendroglioma

A

—”Fried egg” morph
—Delicate “chicken wire” capillaries
—Monomorphic cell forms (vs. highly anaplastic GBM)
—Co deletion of 1p & 19q —> better prognosis that it will respond to chemo

WHO GRADE II-III

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13
Q

Ganglioglioma

A

Tumor of 2 cell types:
—glial tumor in background plus
—Big, funny, occasionally binucleate neuronal forms in tumor
—causes seizures, but favorable outcome w/ surg

WHO GRAD I

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14
Q

Ependymoma

A

—very boring, monomorphic, monotonous cells (not very dysplastic); round, easy to confuse w/ oligodendroglioma or pit. adenoma
—Cells form perivascular formations with nuclear-free area around vessels

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15
Q

PNETs

A

Primitive NeuroEctodermal Tumors (the MEDULLOBLASTOMA family of tumors)

—”small blue cell” CNS tumors
—debate as to how different each type is

Medulloblastomas common in kids
—posterior fossa
—show rosettes histo
**also in this fam: retinoblastoma, pineoblastoma

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16
Q

Meningioma

A

—Psmomma bodies (round collection of calcium; look like tree rings)
—round, pretty, concentric whorls of cells
—pseudo-inclusions in the nucleus
—arise from the arachnoid (e.g. falcine meningioma)
—suprasellar ones killer b/c presses on ICA and CN’s

17
Q

Schwannoma

A

—spindle cell tumor
—lymphocytes involved
—thick-walled BVs
—assoc’d w/ cranial and spinal nerves
—”Verocay bodies” looks to me like necrosis with pseudopallisading but not
—cigar-shaped nuclei
—very indolent, good prognosis; resectable
—often = acoustic neuroma when on CN VIII

18
Q

Path Characteristics of Mets to CNS

A

—sharp edges distinct from brain
—brain/meninges react strongly
—common =(
—can show hemorrhage/necrosis

19
Q

Pituitary adenoma

A

—another fried egg’er (like oligodendroglioma and ependymoma)
—in area of pituitary
—uniform round nuclei w/ abundant cytoplasm
—neuroendocrine symptoms: either abnl or decr hormone release
—bitemporal hemianopsia b/c pushes down on optic chiasm