Neurooncology Flashcards

1
Q

Which three tumors are astrocytomas?

A
  • Pilocytic Astrocytoma
  • Anaplastic Astrocytoma
  • Glioblastoma
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2
Q
Pilocytic Astrocytoma: 
Benin/ malignant? 
Which age group is affected? 
Location in the brain (2)? 
Path feature?
A
  • Benign cystic growths
  • Children/ Young adults
  • Ventricles + Cerebellum
  • Rosenthal fibers (red worm-like)
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3
Q

Anaplastic Astrocytoma:

  • Benign/ malignant
  • Prognosis
A
  • Malignant: higher grade w/ mitotic figures, cytopathic change
  • Aggressive, commonly morph into glioblastoma, death in 5 yrs
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4
Q

Glioblastoma Multiforme:

  • Benign or malignant?
  • How does it present (2)? Age?
  • Prognosis?
  • What is seen pathologically?
  • What is seen radiologically?
A
  • Most malignant brain tumor
  • Presents in 5th-7th decade with seizures or focal deficits
  • Responds poorly to treatment; death in 1 year
  • Pseudopalisading cells with necrotic center
  • Contrast enhancing (ring appearance)
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5
Q

Oligodendroglioma:

  • Location and clinical presentation? Age?
  • Prognosis?
  • Pathological findings?
A
  • Presents in 4th-5th decade of life as supratentoral tumor w/ seizures
  • Responds well to resection, radiation, chemo–survive 5-10 years after dx
  • “Fried egg” appearance of cells
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6
Q

Ependymoma:

  • Age? Location of tumor?
  • Common clinical presentation?
  • Pathologic appearance
  • Radiologic appearance?
A
  • Kids + YA; infra or supratentroal mass–> 4th ventricle (kids) or spinal cord (YA)
  • Obstruction of 4th ventricle–> Hydrocephalus–> Morning HA, vision changes
  • Perivascular pseudorosettes
  • Radiologically, look for them in the fourth ventricle or in the spinal cord
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7
Q

What is the most common spinal cord glioma?

A

Ependymoma = #1 CNS cell tumor of spinal cord

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8
Q

What are the two primitive neuroectodermal tumors?

A
  • Medulloblastoma

- Retinoblastoma

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9
Q

Medulloblastoma:

  • Most common location and age group
  • Common complication?
  • Prognosis?
  • Pathological appearance?
  • Radiological appearance?
A
  • Commonly occur during childhood; found in cerebellum
  • Drop metastasis to spinal cord due to CSF infiltration
  • Responds well to radiation; 5 yr survival 75% w/ tx
  • Homer-Wright Rosettes; small round blue cell tumor
  • Midline cerebellum or spinal cord tumors on radio
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10
Q

Retinoblastoma:

  • Age and location + pathogenesis
  • Clinical presentation
  • Pathological findings
A
  • Childhood, intraocular PNET
  • Deletion Rb tumor suppressor–> tumor–> monocular vision loss w/ loss of red reflex
  • TRUE rosettes
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11
Q

Pituitary Tumors:

  • Most common type + treatment (2)
  • Clinical presentation (2)
A
  • prolactinoma; bromocriptine + transnasal resection

- HA, vision impairment

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12
Q

Meningioma:

  • Type of cells + pathological finding (2)
  • Clinical présentation
  • How to ID on radiology
A
  • Arachnoid cells + PSAMMOMA BODIES
  • Can grow large without causing sx; commonly incidental finding
  • ID on radio w dural tail
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13
Q

Which brain mets are most likely to hemorrhage? (3)

A
  • Renal
  • Choriocarcinoma
  • Melanoma
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