CNS Flashcards

1
Q

maturation pattern in neonate

A

reach adult T1 in 1 yr
adult T2 in 2 yr

inf > sup
post > ant
cent > periphr
sens > motor

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2
Q

what is the last part of the brain mylinate

A

subcortical WM.
occipt > 12 mo
front > 18 mo
FT finsih > 40 mo

PS: BS and post IC > mylinated at birth

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3
Q

MC anomaly ass w/ ACC

A

IH lipoma

mcl: IH 2nd: Quadriq cistern
not tru neoplasm. cong

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4
Q

Iniecephaly

A

extreme retrofelx of the head = star gazing fetus
large for mag
visceral anomaly
short neck

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5
Q

Rhombencephalosynapsis

A

absence of the vermis and continuity of the cerebellar hemispheres, dentate nuclei, and superior cerebellar peduncles.

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6
Q

DW varient vs DWM

A

vermis is hypoplastic in both

vs. DWM:
cerebellum is hypoplastic
no marked hydro
post. fossa is normal in size

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7
Q

meckel gruber syndrome

A

occiptal enchepahlocele
polycystic kid
polydactyl
holoprosnch

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8
Q

azygous ACA

A

lobar HPE

SOD

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9
Q

SOD

A

ab. SP
ab. optic tract
schizencephaly

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10
Q

Dyke-Davidoff-Masson syndrome

A

unlike Ramussen’s encph

there is calv expansion and sinuses pneumotization

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11
Q

mildest form of lissencphaly

A

double cortex band hetrotopia
Xlinked, F>M

classic one is autosomal. M=F, CMV

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12
Q

cobblestone lissencephaly

A

overmigration.
ass w/ congenital muscular dysplasia
retinal detach

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13
Q

hydranencephaly causes

A

HSV is the mcc

2nd: toxo, CMV

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14
Q

IH hypotension

A
Downward displacement of brain through incisura (brain "sagging")
Diffuse dural thickening/enhancement
Veins, dural sinuses distended
Engorged pituitary gland
Subdural hygromas/hematomas
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15
Q

mcl of arachniod cyst

A

middle cranial fossa

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16
Q

NB mets in kids

A

orbit
skull
dura
NOT BRAIN

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17
Q

Pleomorphic Xanthoastrocytoma

A
cortical based, periphral, solid and cyst
Temporal lobe mcl
Supratentorial 
enhancing dural tail, no T2 edema
peds
= DIG
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18
Q

Dysembryoplastic neuroepithelial tumor (DNET)

A
Benign mixed glial-neuronal neoplasm
focal cortical dysplasia
T lobe >> drug resistant seizure 
bubbly appearance  > NO C+
peds < 20
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19
Q

Oligodendroglioma

A

F lobe
1p/19q deletion > gd px
IDH1 > T2/flair mismatch

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20
Q

medulloblastoma ass w/

A

Turcot syn: GBM

Gorlin syn: basal cell navus skin ca, odontogenic cyst

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21
Q

mcc of IV mass in adult

A

central neurocytoma

|&raquo_space; calcify, hetrogen, cystic and solid

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22
Q

mcl of subependymoma

A

4th vent, foramen of monro
homogen C+
might not enhance
soft&raquo_space; no hydro

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23
Q

choriod plexus pap/ca

A

ca only in kids.

adult = 4th vent

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24
Q

Meningoma in nuke

A

+ octerotide

+ Tc-MDP

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25
mcl of dermiod cyst
1st: supracellar cistern 2nd: post. fossa NF-2
26
Hemangiopericytoma
sarcoma mimic aggressive mening invade skull>> but no calc no hyperostosis
27
dysmoplastic infantile ganglioma
large cystic supraten < 1yr. one lobe
28
NPH
> 0.3 evans index | LP: drainage of 30-40 ml
29
porenchephalic cyst
WM lining the cyst | mcc: 2/2 to periventricular hge infarct
30
perivent leukomalacia
wavy countors of lat ven low vol of WM ab SI
31
Joubert synd
ARD molar teeth is high Sn but not Sp. for joubert molar teeth means >> ataxia, develop delay and hypotonia
32
ACC is WNL
- up to 18 wk GA. you cant Dx ACC before that | - agyric smooth app of the brain WNL until 26 GA
33
psuedotum cerebri LP pressure
> 25 mmHg | TRV sinus stenosis is seen up 90%mc
34
mc ass w/ SOD
schizonepchaly
35
earliest manifestation of osmotic demylination
+DWI pons | extrapontine loc might be seen: BG, EC, amygdala, cerebellum
36
Marchiafava-Bignami disease (MBD)
- is a rare CNS disorder alcoholism and malnutrition. - classically involves the corpus callosum with necrosis and demyelination. no ME. - notice WE does not involve CC
37
methanol toxcity
optic nerve atrophy hge putamen WM necrosis
38
CO
GP hypoHU. | T2 bright
39
mc CNS tumor post RTX
meningoma
40
mc brain changes post RTX
vascular mal | cavernoma/teleangectasia
41
Chasing the dragon
Herion | semiovale WM. PL of IC, deep cerebellum WM
42
mcl of MS in children
post. fossa. | M = F
43
most Sn seq for spine and infratent MS
T2
44
subcortical arteriosclerosis encephalopathy
multi infarct dementia that involves the WM. spares U fibers old HTN
45
CADASIL
``` < 40 YO mc heredidatry stroke T lobe >>> classic F and P lobes can be + spares occipital L. ```
46
Hurler's diz
``` lysosomal beaked L1 VB metopic carcniosyn prominant perivascular space macrocephaly ```
47
MELAS
maternally inhertied mitoch dis elev lactate in spectro involves P-O lobes
48
metachromatic leukodystrophy
AR lysosomal | non SP WM + spares U fibers
49
X-linked leukodystrophy
P-O WM
50
canvan diz
``` AR, neonate, poor head control, hypotonia High NAA diffuse WM involve GP thalami spares putamen ```
51
congenital HIV
BG Ca⁺⁺ in (not in adult) Cerebral atrophy >> frontal fusiform vasculopathy stroke subarachnoid hemorrhage
52
congenital HSV encephalitis
hge encephalitis vs Rubella >> ischemia
53
cryptococcus
Dilated PVSs in deep gray nuclei of AIDS patient, no enhancement
54
Brain TB
basilar C+ hydrocephalus vasculitis >> infarct CN involve
55
Most Sn seq for HSV
DWI > T2 you might see bleeding in the adult type
56
west nile
T2 bright BG and thalamus hge pt from saudi
57
CJD = prion diz
Pulvinar sign: post thalamus Hockey stick sign: dorsomedial tthalamus rapidly progressive atrophy gyriform DWI+
58
mcc of epi/subdural empyema
frontal sinusitis
59
cephalohematoma
subperiosteal hematoma elevate the periostum. limited by stutures no CL Sg. mcl: P and O lobes
60
subgalaeal hematoma
not limited space. | underneath galeal aponiorosis
61
sutural diastesis comp in adult
dural venous sinus thrombosis | kids: leptomeningeal cyst
62
mc parasitic diz of the CNS
neurocystoscreosis stage I vesicular: no edema or C+, cystic stage II colliodal: edema C+ stage III grandular less edema and C+. start to calc stage IV: nodular calcified: calc
63
non ketoic hyperglycemia
BG and BS CT hyperdensity T1: high no ME, no C+ looks similar to HE. look at Hx
64
WE
spares BG in adult | common in children
65
opioid overdose, methanol tox
putamen hge necrosis SPARES GP optic nerve atrophy NO tox similar to B12 deficiency >> post col.
66
putamen hge necrosis seen in
methanol cynaide opiod
67
PRESS
involves both cortical and subcortical. P and O lobes DWI is -ve. but sever diz might be +ve
68
HE
acute: b/l symmetric insular and cingulate DWI+ve Bilateral T1WI hyperintensity in basal ganglia (BG), particularly globus pallidus (GP)
69
hypo glu injury
GM > WM CC and IC hippocampus BS, thalami and cerebllum >> spared
70
artery of percheron
paramedian thalami DWI+
71
Recurrent artery of Heubner infarct
Caudate and IC infarct The recurrent artery of Huebner is a br off the ACA. might get clipped during ACOM aneurysm Rx.
72
risk of IC aneurysm rupture
post circ > ant | > 10mm 1% risk of rupture
73
risk of AVM rupture
small small draining v aneurysm BG loc
74
mcc of IC vasculitis
PAN
75
mcc of CVD in the brain
SLE
76
sinonasal polyoposis pattern RF
CF | ASA sensitivity
77
epistaxis
ant nasal septum In max a might be anastomosis between In max a and opthalmic a. pay attension to the eye
78
Parotid gland duct | Stenson
arises from the anterior surface of the gland, traversing the masseter muscle. The duct then pierces the buccinator, moving medially. It opens out into: the second upper molar.
79
Submandibular duct | Wharton's duct
allows the passage of saliva from the submandibular gland to the sublingual papilla located anteriorly. ... It runs forward with lingual nerve and vein and hypoglossal nerve and opens into the sublingual papilla at the side of the frenulum of the tongue.
80
torus palatinus
bony exostosis off the hard palate. WNL
81
Dentigerous cyst = follicular cyst
Benign developmental jaw cyst associated with crown of unerupted tooth 3rd molar >> MCL
82
Keratocystic odontogenic tumor
B9 cystic neoplasm of jaw with aggressive behavior and high recurrence rate no cortical destruction mcc mand tumor
83
Ameblastoma = adamantinoma
``` expansile multiloculated mixed cystic & solid mandible mass, usually near 3rd molar 2nd mcc of mabible tumor arise from dentigerous cyst 5-20% painless ADULT ```
84
odontoma
mcc mand tumor. hamartoma mature solid tum w/ lucent border
85
tornwoldt's cyst
Ovoid, cystic mass in midline nasopharyngeal mucosal space | between longus coli ms
86
warhtin's tum on nuke is +ve on
FDG Tc-Pert Tc-MDP
87
mcc malg partiod tum
mucoepidermiod 2nd: ACC >> perineuoral spread ( melanoma too)
88
Rx of tonsillar ab
ABx PTA: I&D RP abscess >> Sx drainge
89
mcc of cong neck cyst
TGD cyst
90
mcc of 1ry mass in the prestyliod parapharngyeal space
salv gland BMT | mcc lesion is extension from adjacent space
91
pott puffy tumor
OM frontal sinusitis epidural abscess pic
92
nasal glial hetrotopia loc
no connecton w/ IC component | dont C+ much
93
chonal atresia
bony comp is almost alwz | pyriform aperture , 4 mm
94
Dx of CNS vasculitis
Sx BX
95
mc features of VA dissection
arterial stenosis gold Dx: DSA RX; AC if no hge infarct ENV coil, or Sx embolization
96
rever cerebral vasocons synd: RCVS
female SAH >> HA vasospasm of small and med vessels resolve both S&S and img within 3 mo
97
Mx of Cartiod cav fistual
direct: coil, stent or ballon or surgical ligation indirect: conservative
98
moya moya is known as
pial vascular engorgement >> Ivy sign Rx: conservatove, ASA in mild cases. ECA and MCA anastimosis in sever cases
99
venous infarct SI
DWI might be -ve
100
most deadly comp of SAH
vasospasm Dx: angiographic fisher scale Rx; NSAID, CCB, endovasc
101
MCC of septic CS thrombosis
S.aurus fungal in immunocomp Mx: ABx, AC, I&D if needed SOV prominance seen in both CST and CCF
102
IC Amyloid affect which vessels
small and med size vs. MRI is the SOC. sporadic > hereditary ADD
103
Rathke cleft cyst T2 SI?
T2 : hyperintense cyst with a hypointense, intracystic nodule
104
what are the types of hypothalnic hamartoma
parahypothalamic: precausious puberity intrahypothalamic: galaztetic seizure all F/U GM SI. no C+
105
Lymphocytic hypophysitis RF?
1- ipilimumab for metastatic melanoma. immuno Rx 2- Preg 3- post partum so both men and women can get it enlarged. Enhances intensely, uniformly S&S depends on which seg is affected,
106
mcc of Jagular foramne mass
1st: paragan 2nd: shawanoma>> cystic, hge, no bone destruction 3: meningoma >> skull hyperostosis mc nerve > 9
107
inverted pap
more in male high rate of recurrence if not comp resected rare transfor >> SCC
108
where do u measure nuchal thickness?
measured at cerebellum and thalamus | >5 mm 97% Sp for Down
109
features of pulm nodules ass w/ malg
1- semi sold 2- irrg 3- slow doubling 4- lack of calc
110
mc cause of CJD
sporadic | rarely zoontic
111
pointing toward the ventricle GM based mass
DNET >> no C+ | if there DDxL gamglioma, oligo
112
most reliable sign of ch DVT
prior US
113
chrionic pumb ass w/ ?
increased miscarriage X2
114
what is blake's pouch cyst
infravermian cyst that communicates with fourth ventricle
115
dehiscent jugular bulb
sigmoid plate between a high riding jugular bulb and the middle ear is absent, allowing the wall of the jugular bulb to bulge into the middle ear cavity.
116
esthino NB Px ?
good relative to othet H&N ca arise from olf bulb Mx: Sx and Rtx
117
how to differ b9 from path spine fracture ?
``` BM STx post element involve hx of OP but C+ is the least helpful features as both non healed fracture and ca will C+ ```
118
eagle syndrome ? patak syndrome
elongated styliod > 3 cm or cacl styliohyiod lig. CN comp
119
DJD post spinal fusion most common loc ?
mcl >> lumber spine above > lower level of fusion least common T spine 10% of ppl get it
120
normal length of the styliod process ?
2.5 cm | ]> 3 cm Eagle syndrome
121
Esinthenomueroblastoma time of onset ?
2nd and 6th decades peritumor cysts GD px !!!!
122
CADASIL MCL
ant temp lobe
123
MCL of spinal hemangioblastoma
thoracic. eccentric
124
MCL of giant perivascular space
1st: mesoncephalothalaic 2nd: WM
125
earliest finding of Osm demylination
DWI of the pons
126
MCL of inverted pap
lat wall of the nasal cavity, middle turbinate and max ostioum.
127
MCL of allergic fungal sinistis
ethmiod
128
CPA facial nerve shawanoma
super rare. | MCL >> middle ear. dont call CPA mass CN VII shawanoma
129
NF1 mode of inheritance
50% genetic | 50% acquired mutation
130
major reason of M&M w/ SAH
vasospasm
131
Enphesamtous OM organism ?
FusobCetrium Clostridium Enterobacteria GNR
132
MCL of spontaneous RP hge
Psoas ms
133
MCC of B9 cong orbital mass ?
Dermoid > extraoccular
134
MCC extraoccular orbital ca in kids?
rhabdo RB >> INTRAOCCULAR
135
Tolso Hunt dis
IgG4 of the cavernous sinus
136
MCC of spontanous orbital hge
variz
137
MCC of orbital malg
mets
138
MCC of exopthalmus
graves
139
arachnioditis Mx?
``` intrathecal steriod adhesion lysis MCL: L/S pseudomass on myeolgram archnioditis ossificans ```
140
RA vs CPPD
RA: no calc. disc is normal. +ve lig laxity and ADI widening. invagination of the foramnen mag CPPD: calc. psueodumass
141
Wt is the MCC of inherited polyneuropathy?
charcort Marrie tooth diz. type 1: MC one, ADD type II: 2nd mc, Xlinked both motor and senor polyneurpathy fusiform nerve enlargement NNO NO NO C+ Vs: NF1, lymphoma, amyliod or sarciodosis
142
Mx of chrodoma?
Sx + RTx
143
MCC of extradural mass?
mets
144
MCC of intradural extramed?
1st: shawanoma 2nd: menin: MCL: T>C>L
145
shawanoma:
NF2- no malg degen hge + cystic changes common NEVER degen >> ca
146
neurofibroma
target >> non Sp. might undergo malg degen NF1
147
MTx of PNST?
Sx but reccurance is high w/ NF1/2 | presents w/ pain > weakness 2/2 DRG
148
MCL of OO in the spine
L/S
149
VHL Chr?
ADD | Ch.3p
150
MCL of astrocytoma?
T > C long segm 4-7 VB eccentric inflitrative
151
MCL of epend?
C>T | central
152
Rx of aggressive spine hemang?
``` transarterial embol RTx veretroplasty ethanol inj Sx ```
153
MCC of Spine diz in HIV pt?
HIV myelitis T > C. ATROPHY POST col.
154
MCC of CN ab ass/ GBS?
CN VII
155
MCL loc of spine hemangioblastoma
T > C
156
Type I caudal regression?
Sacral agensis > S1 | cord terminates at T11-T12, blunted
157
type II caudal reg?
cocyx agenisis | conus terminates at L3-L4
158
Cong ab ass/ w/ caudal regression
MC GU: renal agensii and hydro MC GI: anal atresia, imper anus VB seg anomaly
159
Wt is block VB?
fusion w/ disc
160
Normal C+ of CNVII?
labyrnith, tympnaic, Ganiculate, mastiod AB: cancicular, cictsernal and extratemporal
161
Weekly QC mr ?
``` Center fr Table position Setup and scanning Geometric accuracy High And low contrast resolution >> phantom Artifact analysis Film quality control Visual check list ```
162
Annual QC mr
B0 homogeneous Slice thickened accuracy and position RF coil Display monitor