31A Adult Brain Tumors Flashcards
What is the plateau wave phenomenon?
- with tumor growth, cranial pressure incr
- eventually, small changes in MAP (due to volume or pressure) = large incr in ICP
- this will affect perf –> focal deficits, MS changes, seizures, etc
General signs/symptoms of CNS tumors?
- HA (incr ICP)
- vomiting (+/- nausea)
- MS changes (depr, apathy, irritability)
- papilledema (MC in kids, young adults)
- seizures
- focal deficits
What HA symptoms should prompt tumor concerns?
- new onset at any age
- worse on wakening, gone in ~hr
- change in character or severity (if chronic)
What vomiting symptoms should prompt tumor concerns?
immediately follows HA onset
What causes the signs/symptoms associated with CNS tumors?
- invasion of neural or vasc structures
- compression of adjacent neural or vasc structures
- Obstr of CNS pathways –> hydrocephalus (incr ICP)
- herniation from mass effect
- cerebral hypoperfusion (incr ICP)
Involvement and pressure on blood vessels can result in:
hemorrhage or CVA
Subfalcine herniation of cingulate gyrus may compress:
anterior cerebral artery and CVA
Diencephalic downward herniation can compress:
Symptoms?
upper brainstem
drowsiness + Horner’s
Uncal herniation causes:
ipsilateral oculomotor nerve palsy and contra or ipsilateral hemiparesis
Upward herniation through tentorium may cause:
ipsilateral oculomotor, Horner (mid position unreactive pupil) and contralateral hemiparesis
Tonsillar herniation causes:
BP changes, weakness, respiratory disturbance, weakness and Horner syndrome
Study of choice when tumor is suspected?
MRI
but CT is more helpful in defining tumor pathology
In T2 MRI, (edema/tumor) spares the cortex
edema
MC 1’ adult tumor?
gliomas
Subtypes of glioma?
astrocytoma, oligodendroglioma, ependymoma
Grade 1 glioma?
Grade 2?
Grade 3?
Grade 4?
1 = juvenile pilocystic astrocytoma 2 = low grade astrocytoma 3 = anaplastic astrocytoma 4 = glioblastoma multiforme
MC type of glioma?
glioblastoma multiforme
Low-grade tumors are MC in:
High-grade tumors are MC in:
younger pts
>50 yo
Grade 1 Glioma:
Malignancy?
Histo?
Trx?
least malig and slow growing
non-infiltrative, ~nml
resection (likely curative)
Grade 2 Glioma:
Malignancy?
Histo?
Trx?
~ slow growing
more abn w/ Rosenthal fibers, can infiltrate
resection, but can recur–sometimes higher grade
(cure unlikely, but survival over many yrs)
Grade 3 Glioma:
Malignancy?
Histo?
Trx?
malignant, fast growing
abn cells, infiltrate adjacent tissue
resection, but tend to recur at higher grade
(cute unlikely, 2-3yr survival)
Grade 4 Glioma:
Malignancy?
Histo?
Survival?
malignant, rapid growing
pseudopalisading pleomorphic appearance, widely infiltrating, neovasc with central necrosis
months
Genetic factor associated with improved survival in oligodendroglioma?
1p and 19q deletions
Epidemiology of meningiomas?
45 y/o F
Meningiomas are derived from:
arachnoid membrane
Locations of meningiomas?
convexity, parasagittal, optic sheath
Prognosis of meningiomas?
Benign, resection often curative
Histo of meningiomas?
spindle cells in whorled pattern, psammoma bodies
Pituitary tumors are MC derived from:
ant pituitary
Pituitary tumors are more likely to secrete hormones if:
<1cm
Pituitary tumors signs/symptoms?
HA
endo dysf
visual defects
facial numbness
What causes facial numbness associated with pituitary tumors?
invasion of cavernous sinus –> CNV compression
What causes bitemporal hemianopsia associated with pituitary tumors?
compression of optic chiasm, starts in upper quad
What causes unilateral blindness associated with pituitary tumors?
optic n compression
What causes diplopia associated with pituitary tumors?
invasion of cavernous sinus –> CN III, IV, VI compression
Origin of auditory neuroma?
Schwann cells surrounding vestibular portion of CNVII
MC locations of auditory neuroma?
int auditory canal or cerebellopontine angle
Epidemiology of auditory neuroma?
middle age (M=F)
Prognosis of auditory neuroma?
benign, slow growing
Signs/symptoms of auditory neuroma?
hearing loss, tinnitus, HA, dizziness, facial numbness or weakness
Bil auditory neuromas =
neurofibromatosis type 2
CNS lymphoma most commonly affects:
leptomeninges + deeper periventricular brain parenchyma
CNS lymphoma trx:
steroids (oncolytic)
Methotrexate (crosses BBB)
CNS lymphoma possible etiology?
EBV in ICH
MC CNS tumor?
mets
MC type of brain mets in males? In females?
lung CA
breast CA
What type of cancer has the highest propensity to met to brain?
melanoma
Prognosis of brain mets?
Untreated = 4wks
Steroids only = 8 wks
Other = up to 1yr
Ddx of ring enhancing lesions?
- mets
- abscesses
- CVA
- high grade glioma
- lymphoma
- demyelination (open/inc)
MC type of extradural spinal cord tumor?
met from breast, lung, prostate, renal CC, lymphoma, sarcoma
MC type of intradural medullary spinal cord tumor in adults? In kids?
ependymoma
astrocytoma