RITE Images 2002 Flashcards

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Demyelination – MS

Gray hue b/c of loss of myelin

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2
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Wet keratin – adamantinomatous craniopharyngioma

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3
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Subacute form of AIDS

Axial T2 weighted image showing diffuse high signal intensity throughout white matter

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4
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Aneurysm – sagittal T1 flow void

Diff dx – pituitary adenoma, meningioma, aneurysm

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5
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Radiation injury vs. recurrent brain tumor -> do FDG PET or Thallium SPECT to differentiate tumor from radiotherapy injury

**The lesion crosses ACA & MCA vascular boundaries & spares the cortex -> not a stroke!

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6
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Ragged red fibers – usually seen in mitochondrial myopathies
Kearns-Sayre myopathy

Werdnig-Hoffman – motor neuron
Duchenne’s – Dystrophin
Central core myopathy – genetic

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7
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Open ring sign w/ enhancement on GAD -> Demyelinating lesion

White matter affected

**Closed rings – GBM, lymphoma, abscess

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8
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Lesion lies in the MOTOR cortex -> frontal lobe

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9
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SDH

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10
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Spinal stenosis – narrowing of dural sac on AP & lateral contrast myelogram

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11
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Pachygyria – cortex is thick

Frontal lobe cortex is flat, white matter in that area doesn’t have the interdigitation

Occurs during 2nd trimester – neuronal migration

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12
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No middle cerebral artery

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13
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VP shunt for NPH

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14
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Optic nerve lesion extending into anterior chiasm -> temporal field defect in contralateral eye

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15
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Vasculitis – affected small & medium sized vessels “beads on a string”

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16
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Negri bodies - seen in rabies

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17
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Subpial corpora amylacea – polyglucosan bodies accumulate w/ age in astrocyte cytoplasmic processes

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18
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Chiasmal glioma

It does NOT arise from the sella

No cystic region or area of signal void to suggest craniopharyngioma

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19
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Multiple brain abscesses

Irregular Ring enhancing; mass effect

(Post-Gad images)

Not hamartomas b/c they would have a central high signal intensity on T1

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20
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Herring bodies in neurohypophyseal tissue;

  • Axonal storage sites for oxytocin & vasopressin
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21
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Cyst is contiguous w/ 4th ventricle resulting from surgical excision of cerebellar astrocytoma

Hemangioblastomas – 2 of 3 which may contain cysts

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22
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GBM – post GAD, intense homogeneous, nodular, ring-like enhancement, encloses a central isointense necrotic core & delineates the gross tumor margin

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23
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Myxopapillary ependymoma

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24
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Focal conduction block of CMAP from demyelination in CIDP

Decreased amplitudes w/o axonal involvement

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25
Intraparenchymal hematoma – high density mass w/ edema
26
**Myokymic discharges** – rhythmic & can be seen as singlets or multiplets; sometimes assoc w/ _K+ channel antibodies_
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**Metachromatic leukodystrophy (MLD)** – \*white matter demyelination w/ spared U-fibers! Confluent periventricular demyelination also can be adrenoleukodystrophy & Krabbe’s
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Agenesis of corpus callosum
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**AD SCA Type 6** –pure cerebellar atrophy predominantly superior vermis \*NO pontine atrophy to suggest olivo-ponto-cerebellar atrophy & Machado Joseph disease; \*NO downward displacement of cerebellar tonsils & posterior fossa is not smaller than normal -\> r/o ACM \*NO subarachnoid cyst b/c no cerebellar compression
30
A-comm artery aneurysm
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**Astrocytoma** – infiltrating neoplasm – b/c the mass in the parasagittal parietal & occipital lobes extends into splenium of CC \*NOT PCA infarct b/c it wouldn’t cross midline \*NOT acute hematoma b/c it would be hypointense on both T1 & T2
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Non-communicating/obstructive hydrocephalus
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Thrombus in Vein of Galen & Straight sinus – abnormal hyperintensity on T1 & axial proton density images; hemorrhagic infarction in B thalami
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B frontal contusions w/ slight orange tinge 2ndary to presence of residual hemosiderin-laden macrophages
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Lacunar infarcts
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Oligodendrogliomas
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Reversible posterior leukoencephalopathy – found in pts w/ malignant HTN Found in 85% of patients studied w/in 72 hrs after onset of sx
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Spinal stenosis - Constricted spinal canal 2ndary to degenerative facet joint disease \*no disc herniation or synovial cyst present
40
Herniated disc
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Myxopapillary ependymoma
42
**AVM** – need to follow up w/ cerebral angiogram \*this is a contrast enhanced CT showing a large lobulated densely enhancing structure medial to the Sylvian fissure w/ a large serpiginous structure leading from lesion posteriorly towards the vein of Galen -\> need to follow up w/ angiogram
43
Communicating hydrocephalus
44
**Discitis** -pt had documented E. faecalis osteomyelitis affecting L2/L3; ring enhancing
45
Wernicke’s encephalopathy / thiamine deficiency; mammillary bodies congested & discolored
46
**Toxoplasmosis** – ring enhancing, multiple & located in deep central grey nuclei or lobar G/W jxn. - Iso to hypointense on T1 & hyperintense on T2 w/ mass effect & edema - You need the question stem
47
**Lambert eaton syndrome** – incremental response cof CMAP of \> 200% following exercise w/ or w/o decrement on repetitive stimulation
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**Creutzfeldt astrocyte** – multiple small nuclei (micronuclei) & abundant eosinophilic cytoplasm \***seen in demyelinating disease**
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Germinoma – most common pineal region tumor
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**Sagittal sinus venous thrombosis** – infarction w/ hemorrhage over an area of extensive cortex & in underlying white matter \*venous thrombosis assoc w/ hypercoaguable state & severe dehydration
51
Carbon Monoxide poisoning
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**Subdural hematoma** \*pt presented w/ symptoms after recovery from anesthesia & is bright on T1 & T2; well known complication of spinal anesthesia & LP
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Leptomeningeal melanocytes
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DNET Dysembryoplastic neuroepithelial tumor
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**Suppurative ventriculitis** – abnormal ependymal enhancement & CSF hyperdense, white matter w/ marked edema
56
MS
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**meningothelial (arachnoid) cell cluster** in the fibrovascular stroma of choroid plexus -\> *occasionally give rise to meningiomas (intraventricularly)*
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**Pleomorphic xanthoastrocytoma** – large cyst w/ mural nodule; - usually found in temporal or parietal lobes - Surrounded w/ minimal hemosiderin rim
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**Vein of galen aneurysm** – congenital anomaly
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**Metastatic disease** – large mass lesion filling right orbit, compressing & deforming posterior margin of globe; lateral wall of maxilla is destroyed & is assoc w/ soft tissue mass
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**Neurofibroma or meningioma** -\> surgical removal Do not need to do CT myelogram \*intradural extramedullary
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**Subacute hemorrhage** 2ndary to **infarct** (not AVM b/c it would have been bigger) \*high signal on T1
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**Locus ceruleus** – source of NE projections
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**Pornecephalic cyst** – lesion partially covered by arachnoid & extends from SAS to ventricular system; smooth walled & surrounded by abnormal radially oriented gyri
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**Hyper-dense MCA sign** - Acute thrombosis of LMCA – acute MCA infarction (also look for subtle L cerebral sulcal effacement, hypodensity on L side) Hyperdensity – due to either calcific or hemorrhagic components of acute plaque
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**Chronic HSV encephalitis** Encephalomalacia in both temporal lobes; can have cystic changes Hyperintensity in temporal lobes
67
**Neurofibrally tangle** – intraneuronal intracytoplasmic inclusion composed of paired helical filaments AD, PD, PSP, Down’s, PD complex of Guam, post-encephalitic Parkinsonism
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**SDH** – no need for further testing à craniotomy now!
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**MS plaques** – focal demyelination Not epyndemoma à you’d see focal mass w/ cord enlargement
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Hematoma – 2 weeks or more in age \*if you see bright on T1 & rim w/ bright on proton density weighted images (b/c of hemosiderin in macrophages surrounding hematoma) --\> methemoglobin
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* *Centrotemporal spikes** - * *Benign rolandic epilepsy of childhood;** clonic movements of face & hand that often progress to more generalized seizure
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Proximal internal carotid artery has a rounded stump w/ no distal flow -\> **occlusion** b/c of atherosclerosis
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String of beads -\> **Fibromuscular dysplasia (FMD)** Characteristically FMD extends from C1-2 to entrance of ICA into petrous carotid canal; 1/3 are assoc. w/ intracranial aneurysms Common patients are young females (age 25-50).
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**Meningioma** – intradural, extramedullary \*ependymoma, astrocytoma & hemangioblastomas – intramedullary lesions
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**Arachnoid cyst** – (lesion @ tip of L temporal lobe) -\> spares cortical ribbon & extraaxial -\> r/o head trauma or HSV; the **lesion looks like CSF**
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**Dandy Walker Malformation** – no vermis , 4th ventricle connects w/ cisterna magna, posterior fossa enlarged
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Ependymoma – perivascular pseudorosettes
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**Onset latency** in sensory nerve action potential; initial positivity is the AP passing beneath the active recording electrode
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**Jitter** on single fiber EMG -\> disease in neuromuscular transmission (**MG**) & denervating neuropathy (**ALS**) ;
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Cervical portion of carotid -\> C – petrosal segment of carotid artery -\> cavernous portion A – P-comm B – distal ICA D – ACA E – A-comm
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A – sylvian/lateral fissure / circular sulcus region – separates frontal & temporal lobes B – trigone /atrium of lateral ventricle C – genu of corpus callosum D – frontal paranasal sinus E – subcutaneous fat