Neuro Flashcards
(242 cards)
patterns of PRES
- parieto-occipital lobes
- holohemispheric at watershed zones
- superior frontal sulcus
difference between porencephaly & schizencephaly
- porencephalic cyst CSF filled lined with reactive gliosis
2. schizencephaly lined by grey matter
carbon monoxide poisoning
bilat globi pallidi necrosis
what lines virchow-robin spaces
pia
HIV encephalitis
- progressive atrophy and symmetric, periventricular or diffuse patchy/confluent white matter disease
- characteristic sparing of the subcortical-U fibers
cribriform plate is in the superior aspect of what bone?
ethmoid
which show restricted diffusion?
medulloblastoma, ATRT, ependymoma
medulloblastoma
ATRT
contents of meckels cave
CSF (90%)
fascicles CN V
trigeminal/semilunar/Gasserian ganglion
(posterolateral to cavernous sinus)
only nerve to exit dorsal brainstem
CN IV
trochlear
tram track calcification along optic nerve
optic n meningioma
recurrent laryngeal nerve sits in here bilaterally
tracheoesophageal groove
bilat vestibular schwannomas
NF2
NF2 mutation
22q12
artery of percheron infarct
central midbrain
medial thalami
NF 1 mutation
17q11.2
auto dom
100% penetrance
antibody in neuromyelitis optica
anti NMO IgG
against aquaporin 4
CN nuclei in the medulla
CN 9, 10, 11, 12
CN 7 nuclei
mid pons
normal T1 signal vertebral bodies
brighter than disc
stages of neurocysticercosis
- Vesicular (viable larva): small 10mm cysts w scolex, follows CSF, no edema
- Colloidal (dying larva): inflammation, hyperintense to CSF, enhancement, surrounding edema
- Granular nodular (healing): cyst involutes, wall thickens, edema ↓
- Nodular calcified (healed): no edema, MR black dots
cause of neurocysticercosis
taenia solium
findings of NFI
‘substance’
- waxing/waning WM lesions (UBO, FASI)
- optic n glioma
- optic pathway glioma
- brain gliomas (brainstem, cerebral, basal ganglia)
- [plexiform] neurofibroma
- vascular dysplasia
- cafe au lait spots
- dysplastic skeletal lesions
findings of NFII
‘layers’
- multiple CN schwannomas
- meningiomas
- spinal tumors/ependymomas
MISME - multiple inherited schwannomas meningiomas and ependymomas
clinical criteria of NFI
2+ of:
≥ 6 café au lait spots ≥ 15 mm adults or 5 mm children
≥ 2 neurofibromas or 1 plexiform neurofibroma
Axillary/inguinal freckling
Visual pathway glioma
≥ 2 iris hamartomas (“Lisch nodules”)
Distinctive bony lesion (sphenoid wing dysplasia, thinning of long bone ± pseudoarthrosis)
1st-degree relative with NF1