Neurooncology Flashcards
1
Q
Which three tumors are astrocytomas?
A
- Pilocytic Astrocytoma
- Anaplastic Astrocytoma
- Glioblastoma
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)
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
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)
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
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
7
Q
What is the most common spinal cord glioma?
A
Ependymoma = #1 CNS cell tumor of spinal cord
8
Q
What are the two primitive neuroectodermal tumors?
A
- Medulloblastoma
- Retinoblastoma
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
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
11
Q
Pituitary Tumors:
- Most common type + treatment (2)
- Clinical presentation (2)
A
- prolactinoma; bromocriptine + transnasal resection
- HA, vision impairment
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
13
Q
Which brain mets are most likely to hemorrhage? (3)
A
- Renal
- Choriocarcinoma
- Melanoma