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147 Cards in this Set

  • Front
  • Back
Differential Dx of Basal Ganglia Lesions?
Infection
toxoplasmosis
cryptococcus
cjd

toxic/metabolic
epm
wilson's disease
leigh's disease

Ischemia
lenticulostriate infarct
hypoxic/ischemic encephalopathy
internal cerebral vein thrombosis

neoplasm
lymphom/leukemia
Differential dx for ring enhancing lesions
Metastases-mult g-w jxn

Abscess-+dwi, thin c+

Glioma-likes cc and deep wm

Infarct-usually gyriform c+, except cbl, and bg

Contusion-t1 shortening and susceptibility

Demyelinating disease-incomplete ring c+, little mass effect

Radiation necrosis-no perfusion

atypical infection-tb, neurocystercicosis, fungal

toxoplasmosis versus lymphoma-immune status
Cerebellopontine angle mass
Schwannoma
Meningioma
Ependymoma
Lymphoma
Inflammatory d/o
Metastases
Clival mass
Chordoma
Chondrosarcoma
Plasmacytoma
Metatases
Lymphoma
NOF
Diffuse marrow signal abnormality
Chronic anemia
infiltrative processes ie leukemia, lymphoma, and sarcoid
bone dysplasias
Most common neoplasms of the orbit
cavernous hemangioma
capillary hemangioma
lymphangioma
high signal intensity along apex of pituitary stalk at floor of third ventricle
tuber cinereum lipoma
absence of normal posterior pituitary high signal
lch
hemosiderosis
ectopic pituitary
connective tissue disorders associated with dislocations and/or subluxation of the lens
marfan's
ehrlos danlos
homocystinuria-inferior
parotid lesions
benign mixed tumor (pleomorphic adenoma)
warthins tumor (cystic/solid, parotid tail)
mets
mucoepidermoid carcinoma
adenoid cystic carcinoma (cn 7 spread)
Enhancing mass at jugular foramen
glomus jugulare
mets
schwannoma
nasopharyngeal carcinoma
meningioma
chondroid lesions or chordoma
Cyst in 3rd ventricle
ependymal cyst
arachnoid cyst
colloid cyst
cystersicosis
epidermoid cyst
cystic neoplasm
Hyperdense T1 lesions
cavernous malformation
hemorrhagic mets
metastatic melanoma
amyloid angiopathy-subcortical
htn
DAI-subcortical, hx of trauma
midline posterior fossa mass in kids
pnet
ependymoma
cerebellar astrocytoma
oligodendroglioma
tram track enhancement of the nerve sheath
meningioma
sarcoid
lymphoma
mets
pseudotumor
pituitary mass lesions in pituitary stalk
lch
germinoma
infection(meningitis/tb)
lymphoproliferative d/o
occ sarcoidosis
glioma
lymphocytic adenohypophysitis
expansile mass of the petrous apex
mucocele
cholesterol granuloma
multiple myeloma
mets esp renal/thyroid
chondrosarcoma
cn v schwannoma
enhancement of the optic nerve
optic neuritis
sarcoid
infection
primary tumor ie glioma or meningioma
mets
devics disease
basilar invagination
ra
fibrous dysplasia
pagets
renal osteodystrophy
cd
osteomalacia
platybasia
achondroplasia
osteogenesis imperfect
ro
pagets
cleidocranial dysplasia
down's syndrome
painless proptosis
thyroid opthalmopathy
cavernous malformation
mucocele or polyposis
painful proptosis
pseudotumor
abscess
cellulitis
lymphoproliferative lesions
thyroid opthalmopathy
sarcoidosis
wegeners
diffuse dural enhancement
mets
leukemia/lymphoma
granulomatous disease
-leukemia, sarcoid
-wegeners
-erdheim chester
-lipid granulomelosis
spontaneous intracranial hypotension
idiopathic hypertrophic pachymeningitis
ill-defined low attenuation mass lesion on ct
glioma
demyelinating disease
encephalitis
neoplasms that arise from the lateral ventricle along foramen of monroe or septum pellucidum
oligodendroglioma
central neurocytoma
fibrillary astrocytoma
pilocytic astrocytoma
ependymoma
hemangioma
subenpendymal gc astrocytoma
choroid plexus papillloma
pontine hyperintensity
ischemia
infection
brainstem glioma
demyelination
myelinolysis
pml
basal ganglia ca++
endocrine
metabolic
congenital/developmental
inflammatory
toxic
pediatric bg ca++
fahr's syndrome
hypo/hyperparathyroidism
MELAS
HIV
High density in subarachnoid space
blood

cellular material ie carcinomatosis, infection, sarcoid

iodinated contrast-ie in renal failure

CSF hypotension-check for sd collxns and large dural sinuses

anoxia-?dense venous stasis, see in leptomeninges as well, white cerebellar sign, bg indistinct
confluent white matter lesions in adult
demeylinating disease
neoplasm
PML
microvascular ischemic disease
autoimmune mediated vasculitis
confluent white matter lesions in a child
adem
ms
dysmeylinating disease (leukodystrophy)
pineal masses
pineal cyst
germ cell tumor
pineal cell tumor
meningioma
tectal plate glioma
sellar/suprasellar mass in child
craniopharyngioma
germ cell tumor
rathke cleft cyst
optic nerve/hypothalamic glioma
hypothalamic hamartoma
posterior fossa mass in an adult
infarction
mets
hemangioblastoma
vascular malformation
htn hemorrhage
posterior fossa cyst
mega cisterna magna
arachnoid cyst
dandy-walker malformation
joubert syndrome
csf fluid lined cortical defect
prior infarct
schizencephaly
porencephalic cyst
enhancing intramedullary spinal mass
ependymoma
astrocytoma
hemangioblastoma
mets
demyelinating disease
intradural extramedullary spinal mass
nerve sheath tumor
meningioma
csf mets
diffuse temporal lobe mass
herpes encephalitis
ischemia/infarction
gliomatosis cerebri
limbic encephalitis
status epilepticus
increased T2 signal intensity in the basal ganglia/thalami in child
ischemia
co poisoning
wilson's disease
mitochondrial disorder
kernicterus
osmotic demeylination
intraparenchymal hemorrhage
htn infarct-basal ganglia, pons, cerebellum
vascular malformation
hemorrhagic infarct-lobar, venous
hemorrhagic neoplasm
contusion
cerebral amyloid disease-typically lobar
corpus callosum lesion
gbm
lymphoma
demeylinating disease
dai
marchiafava bignami disease
subependymal nodules
ts
heterotopic gray matter
torch
mets
mass supratentorial csf collection in newborn
massive hydrocephalus
hydrancephaly
alobar prosencephaly
agenesis of cc with midline interhemispheric cyst
bilateral open-lip schizencephaly
intraventricular mass
meningioma
choroid plexus tumor
central neurocytoma-enhances
ependymoma/subependymoma-subep doesn't enh
colloid cyst
subependymal gc astrocytoma
cerebellar atrophy
alchohol abuse
anticonvulsant therapy
paraneoplastic syndrome
sporadic olivopontocerebellar atrophy etc
spinal cord signal abnormality
demyelinating disease
cord contusion
intramedullary neoplasm
transverse myelitis
cord ischemia
cortically based enhancing neoplasm
oligodendroglioma
astrocytoma
ganglioglioma
dysembryoplastic neuroepithelial tumor
desmoplastic infantile glioma
epidural spinal mass
disk extrusion
epidural hematoma
epidural abscess
mets
epidural lipomatosis
synovial cyst
prominent periventricular/basal ganglia cystic lesions
virchow-robin spaces
lacunar infarct
infection
cystic neoplasm
neuroglial cyst
Approach to CNS infections
extra-axial
ring enhancing
temporal lobe
basal ganglia
white matter

imaging characteristics

clinical history, immune status, age, chronicity of symptoms, geographic region
ddx subdural epyema
effusion-nml dwi, no c+

chronic sdh - susceptibility on MR

hygroma-trauma history
ddx bright sas on flair
tumor
meningitis (pus)
sah (blood)
slow flow-ie pial collateral with carotid stenosis
oxygen therapy
ddx basilar C+
tb
fungal
sarcoidosis
acute bacterial or viral leptomeningitis
c+ over cerebrum
chronic fungal or tb
c+ basilar cisterns
pachymeningeal enhancement
idiopathic hypertrophic cranial pachymeningitis
intracranial hypotension
dural metastasis
infection
sarcoidosis
leptomeningeal enhancement follows sulci and basilar cisterns
meningitis
leptomeningeal tumor
sarcoid
Stages of neurocysticercosis
vesicular-larva in a clear cyst (cyst with dot), no edema
colloidal vesicular-scolex degen, edema, c+, t2 hyperintense with dark rim
granular nodular-cyst wall thickens, decreased inflam
nodular calcified-lesion mineralizes, no edema
ddx temporal lobe lesions
mca infarct
low grade glioma
gliomatosis
ddx white matter abn
chronic small vessel disease
radiation/chemo
transependymal csf
ms/adem
hiv encephalopathy
cmv
pml
subdural hematoma
stops at midline
crosses sutures
don't see dura

crescent shaped
countrecoup

4 bad signs
heterogenous
increased mass effect
convex
SAH
epidural hematoma
heterogeneity-ie low density means active bleeding, ie swirl sign
enhancing traumatic hematoma
clues-bilateral, orbitofrontal, hemosiderin ring, other injuries, can enhance
coup-contrecoup injury
coup site-fracture, edh

contrecoup-sah, sdh, brain injury
DAI
grade 1-lobar white matter

grade 2-splenium of corpus callosum

grade 3-triad
lobar wm
corpus callosum
dorsolateral brainstem
venous htn + hemorrhagic CVA
can mimic DAI
important skull fractures
overlies a dural venous sinus-hem infarct

overlies the MMA-epidural hematoma

overlies eloquent cortex

depressed>table width

open/compound- ie get infected

tranverses ICA canal-pseudoaneurysm, dissection

temporal bone fracture
carotid cavernous fistula
proptosis

enlarged EOM

convex cavernous sinus

enlarged superior opthalmic vein

retrobulbar fat stranding

can get hemorrhagic venous infarcts
traumatic CCF
high flow shunt with direct connect between ica and cavernous sinus

chemosis, proptosis, bruit, cranial nerve pasly, decreased vision, ha

tx-manual cratoid jugular compression; transarterial endovascular embolization (balloon>coils>NBCA)
early nct signs of stroke
losss of gray-white matter differentiation
cortical (insular) ribbons sign
basal ganglia effacement
hypodensity
dense artery sign
look up stroke changes per hours
?
vascular territories
aca-supplies cingular and superior frontal gyrus

mca
deep-lenticulostriate from m1 segment which supply basal ganglia
superifical-frontal, parietal, temporal lobe and insula

pca-thalamus, mesial temporal lobe, occipital lobe in calcarine region, doesn't extend about ventricles

basilar-posterior fossa, bilateral cerebellar hemispheres, pca territories

anterior choroid artery-amygdala, hippocampus, internal capsule up to the ventricles, suspect when face, arm, leg all affected
carotid dissection
proximal
progression of aortic dissxn
common carotid artery
ica extension uncommon
false lumen
asx or symptomatic

distal
mid to distal ica
carotid bulb spared
no false lumen
subintimal hematoma
symptomatic
hemorrhagic venous infarcts vascular territories
patchy areas of hemmorhage surrounded by edema

superior sagittal sinus and cortical vein-parietal lobe

staight sinus, internal cerebral veins-bilateral thalamus

transverse sinus + vein of labbe-temporal lobe

cavernous sinus
simplified histologic subtypes of brain tumors
primary tumor of brain-glioma

primar tumor of brain coverings-meningioma

primary neuronal tumors-neurocytoma

primary tumors of primitive cells (medullo, PNET)

secondary tumors (mets)
look for tumor related complications
hydrocephalus
hemorrhage
herniation
cyst with noduel and minimal surrounding edema lesions
pilocytic astorcytoma
ganglioglioma
pxa
hemangioblastoma
imaging of tumors
glioblastoma multiforme
most common primary glioma

who grade IV

older

supratentorial white matter

irregularly enhancing mass with central necrosis and edema

poor px

highly vascular and infiltrative
fibrillary astrocytoma
low grade vs anaplastic
better px than gbm
usually younger for low grade
eventually degenerate

who grade 2-no enhancement

who grade 3-some enhancement
juvenile pilocystic astrocytoma
who grade 1
peds or young adults
excellen px dep on location

well circum with cyst and min edema
pleomorphic xanthoastrocytoma
rare, distinc astrocytoma subtype, who grade 1

indolent, benign tumor

children, young adults

superficial cortical location

temporal lobe most comon

cyst with mural nodules, minimal edema

good px
oligodendrogliomas
low grade and anaplastic

younger patients

better px than astrocytoma

1p 19q deletion

fronta lobe most common

cortical involvement common, expanding cortex, var enhancement

ca++ common

can appear aggressive
intracranial tumors with ca++
ddx
oligodendroglioma
ependymoma
craniopharyngioma
choroid plexus tumor
meningioma
ependymoma
third most common ped brain tumo

60% infratentorial (4th vent)

when supratentorial, extraventricular location common

ca++ common

anaplastic variant has poor px
meningioma
most common extraaxial tumor

middle aged women

excellent px except anaplastic variant

can be multiple (meningiomata, neurofibromatosis)

can be intraventricular (trigone, most common) or intraosseous

ddx
dural based mets
hemangiopericytoma
solitary fibrous tumor
chondrosarcoma
hemangiopericytoma
rare hypervascular extra-axial tumor

arises from outer layer of meninges, ie pericytes of zimmerman

can occur anywhere in body

tend to be more aggressive than meningioma

usually no dural tail
primary cerebral lymphoma
usually nonhodkin, b cell

usually adults

multiple enhancing masses in deep gray or white matter and periventricular location

maybe centrally necrotic in immune compromised patients

tends to involve same place as glioma

tend to have fairly low t2 signal int and mildly reduced diffusion
brain tumors with low t2 signal
cellular tumors and high nuclear to cytoplasmic ration

ddx
lymphoma
pnet, medullobllastoma
meningioma
mucinous adeno met
intraventricular mass with attacment to septum
central neurocytoma-enhances, vascular

subependymoma-doesn't enhance
pediatric brain tumors
medulloblastoma-tends to met early on

juvenile pilocytic astrocytoma

choroid plexus papilloma

craniopharyngioma

pleomorphic xanthoastrocytoma
csf dissemination
pnet
medulloblastoma
pineoblastoma
ependymoma
choroid plexus ca
choroid plexus papilloma vs carcinoma
usually in young children

lateral ventricle in children, fourth ventricle in adults

avid enhancement and ca++ common

hydrocephalus
diffusion positive mass lesions
ddx
epidermoid

mucinous adeno ca met

abscess

cellular tumors ( ie lymphoma, pnet, meningioma)
epidural empyema (or abscess)
extension from sinus
bony erosion
valveless bridging veins
lentiform shape
frontal sinus most common
complications
dural sinus thrombosis
osteomyelitis
meningitis
subdural empyema
high mortality

10% brain abscess, sinus thrombosis

young kids-meningitis

adults-paranasal sinuses

bright dwi

location
convexity 50%
parafalcine 20%

ddx
effusion-nml dwi, no c+
chronic sdh-suscept on mr
hygroma-trauma hx
complications of meningoencephalitis
infarct
hydrocephalus
subdural empyema
dural sinus thrombosis
leptomeningitis
ct
insensitive, pre-LP

mri
flair and gad-sas abn
dwi-infarct and subdural emphyema
factors favoring abscess over neoplasm
asymmetric collagen dep->thinner rim c+ toward ventricle->propensity for iv rupture

daughter cysts

light bulb bright diffusion

thin smooth c+ rim

t2 hyperintense center with dark rim (free radicals)
caseating brain tuberculoma
dark t2 signal, abn chest xray
ADEM
multifocal BG and WM

10-14 days after infection/vacc

maybe tumefactive

minimal mass effect

punctate, ring, and incomplete enhancing
invasive aspergillosis of the brain
enhancement
immunocompromised-min
immunocompetent-ring c+

angioinvasion by hyphae
hemorrhage, septic infarcts, aneurysms
dark t2 hemorrhage

minimal mass effect

direct from sinuses or hematogenous ie lungs

dwi variable
hsv encephalitis
mesial temporal lobe->limbic system
insula, inferior frontal, cingulate, spares bg

bilateral, asymmetric

patchy c+ early, and gyriform c+ later

dwi+
progressive multifocal leukoencephalopathy
subacute demyelinating
jc virus
asymmetric
subcortical U, deep wm
dark t1 signal
location
parieto-occipital
bg, brainstem, cerebellum
cmv
ventriculoencephalitis
cd4<50
chorioretinitis in 25% aids
mri-thin pvwm t2 and subependymal c+
cryptococcus
meningitis
5-10% aids
gelatinous pseudocysts
dilated vr spaces
nonenhancing
bg and thalami
ica dissection
neck pain, embolic events, horners, cn12 palsy

t1-fs

spontaneous or posttraumatic

ica (spont)-above bifurcation

ica (traumatic)-distal cervical and skullbase

vert c1/c2

irreg in sites unusual for athero
string sign
aneurysmal dilatation
occlusion
intimal flap
nontraumatic intraparenchymal hemorrhage
underlying lesion
tumor-solic c+
avm-cta
cavernoma-look for dva
aneurysm-cta
amyloid angiopathy-spares bg
dural venous sinus-subcort. wm
hypertension-bg, pons, cbl
coagulopathy
multiple brain ca++
cavernomas
neurocysticercosis
prior infection ie toxo
multiple foci of susceptibility in the brain
amyloid angiopathy
htn
cavernomas
shear injury
cavernomas
discrete collection of endothelial lined sinusoids "caverns"
no intervening brain
recurrent intralesional hemr.
vascular hamartoma
0.25-1%/year hem risk
75 sporadic
10-30% familial
angiographically occult
assoc DVA

mr
hemosidern ring "black halo"
popcorn t2 hyperintensity
t1 hyper and hypo locules
minimal or no c+

ct
>50% calc
dva
no mass effect
capillary telangiectasia
brainstem
assoc with radiation
no t2 signal usually, unless big
brush c++
dark GRE
don't touch
spetzler-martin grading
size of avm nidus (compact or diffuse)
<3cm-1pt
3-6cm-2pts
>6cm-3pts

eloquence of adj brain
eloquent-1 point

pattern of venous drainage
superficial-0
deep-1

tx
surgical resection
gamma knife <3cm
embolization
classic avm
98% solitary or sporadic
2% multiple and syndromic (hht)

1-4% bleeding risk per year

increased bleeding risk with
feeding artery 15%, nidus aneurysm 50%
venous stenosis
deep location or drainage
smaller nidus

ct
25-30% ca++
iso/hyperdense vessels

mri
bag of worms
no mass effect
t2 gliosis
ICA and ECA anatomy
look up ct, mr, angiogram
pcomm aneurysm/sah
cta to find aneurysm

look for 2nd and 3rd aneurysms

3rd nerve palsy

complications
hydrocephalus
vasospasm
intracranial aneurysm risk factors
smoking, cocaine, >50, f

family hx

fibromuscular dysplasia

anatomic variants (ie trigeminal artery)

type IV ehlers-danlos

nf1

adpckd
perstistent trigeminal artery
fetal connection of cavernous carotid to upper 1/3 basilar artery

ddx
fetal pca-supraclinoid ica above sella
dural sinus thrombosis
ct-hyperdense and expanded sinus, empty delta sign post c+

mr-loss of normal flow void
flair pitfall-acute dst dark
tof mrv pitfall-t1 shortening

pattern of venous ischemia
sss-parasagittal
tranverse-temporal lobe
deep-bithalamic
venous infarcts
subcortical white matter
hemorrhage
doesn't follow arterial dist
+/- reduced diffusion
maybe mass like and mimic
neoplasm
moya moya
idiopathic progressive arteriopathy of childhood

occ of supraclinoid IC and prox cow

moya moya like-sickle cell, NF, radiation, atherosclerosis, drugs

angio-puff of smoke, cloudlike lenticulostriate collaterals

ct/mr-bg and leptomeningeal c+ due to collateral slow flow

peds-ischemia

adults-hemorrhage
indirect CCF
low flow
meningeal branches
dAVF
spontaneous, can be observed
direct CCF
high flow
tramua, aneurysm rupture
direct
usually needs more direct tx
elevated ICP
primary (idiopathic)
idiopathci intracranial hypertension
aka pseudotumor cerebri

secondary
intracranial mass
diffuse cerebral edema
dural sinus thrombosis

nl csf pressure-80-150 mmh20
idiopathic intracranial htn
mostly women, 3rd decade

obese, recent weight gain

maybe med induced

papilledema->optic neuroopathy

headaches, transient visual obscurations, diplopia, pulsatile tinnitus

empty sella
narrowed mid transverse sinuses

slitlike ventricles
infarcts in young patients
cardiac-ie congenital hd, valve dz, la myxoma

prothrombotic d/o-ie ss, protein s or c, or antithrombin deficiencies, factor 5 leidin, lupus anticoagulant, polycythemia, platelete disorders, leukemia, chemotherapy related

inherited-
vascular-neurocutaneous synd, cadasil
metabolic-melas, homocystinuria

acquired vascular d/o
dissection, NAT, moya moya, systemic or cns angiitis, migraines
ocp, street drugs
MELAS
mitochondrial myopathy
encephalopathy
lactic acidosis
stroke like episodes

2nd dec

headache, psychosis, acute stroke like cortical lesions that cross usual vascular territories
most often parietal and occipital

dwi variable
strokes, seizures

mrs-inc lactate in csf and in "normal" brain
PRES
acute encephalopathy

ct
bilateral white matter hypodensity

mr
bilat predom white matter hyperintensity
post fossa, parietal, occipital, and posterior frontal and temporal lobes
neg dwi indicates that this is vasogenic edema

assoc conditions
htn
eclampsia/pre-eclampsia
acute gn
hus
ttp
cvd
seizures
drug toxicity
tacrolimus fk506
cyclosporine
erythrpoietin
cisplatin
myelination pattern
caudal to cephalad
dorsal to ventral

t1 changes before t2
t1 mature by 8 mo
t2 mature by 2 y
agenesis of corpus callosum
medial sulci radiate to high riding 3rd ventricle

everted cingulate gyri

dilatation of the lateral ventricles, without true hydrocephalus
hypogenesis of the corpus callosum
corpus develops from front to back
midline lipomas
dont touch

interhemispheric

quadrigeminal plate/supracellar cistern

suprasellar/interpeduncular cistern

cerebellopontine angle

sylvian cistern

signal suppresses with fat sat
hypothalamic hamartoma
insointense to gray matter, nonenhancing

present with precocious puberty, gelastic seizures
complete lissencephaly
agyria, assoc with chromosomal anomalies
incomplete lissencephaly
pachygyria

chromosome anomalies
band heterotopia
band of neurons located in white matter, follows gray matter signal intensity on all sequences and separated from cortex by myelinated white matter

sons can get classical lissencephaly
polymicrogyria
disorganization or absence of layers of cortex

look like thickened cortex, but has multiple small gyri

perisylvian/sylvian regions on sagittal images which are abnormally deep

seizures +/- focal deficits/developmental delay

genetic or acquired (in utero ischemia, infection)
periventricular nodular heterotopia
isointense to cortex, nonenhancing

smooth, line ventricle

if ovoid, long axis is parallel to ventricle

may project into lumen of lateral ventricle
schizencephaly
communication b/w sa space and ventricle

lined by dyplastic gray matter, polymicrogyria

open lip when walls of cleft are separated versus closely opposed


bilateral
congenital or acquired
often septum pellucidum absent


unilateral or bilateral

worse outcome when bilateral, open lip
alobar holoprosencephaly
monoventricle

nonseparation of forebrain
semilobar holoprosencephaly
lack of separation of forebrain

callosal hypogenesis

only condition where posterior callosum maybe formed without anterior callosum
chiari 1 malformation
low position of cerebellar tonsils (5mm below foramen magnum)

pointed morphology

r/o other causes of tonsillar descent-intracranial hypotension, mass, increased intracranial pressure

look for associated syrinx
chiari 2 malformation
small posterior fossa

myelomeningocele

hydrocephalus after closure of MMC

tectal beaking

interdigitation of gyri

callosal hypo/agenesis

cortical malformations
dandy walker malformation
large posterior fossa

hypogenesis/agenesis of the vermis

cystic dilatation of the 4th ventricle

continuum with mega cisterna magna (normal vermis)

dwm
hydrocephalus
callosal hypo/agenesis
occiptal encephaloceles
cortical malformations
syrinx
pediatric sellar/suprasellar masses
glioma
craniopharyngioma
germ cell tumor
histiocytosis
hypothalamic hamartoma of tuber cinereum
pit adenoma
rathke cleft cyst
orbital masses in children
abscess

pseudotumor

benign tumors
dermoid, epidermoid, teratoma, neurofibroma

malignant tumors
rhabdomyosarcoma, retinoblastoma, optic glioma, lymphoma/leukemia, histiocytosis, mets

vascular malformation

fibrous dysplasia

graves disease