RITE Images 2002 Flashcards

1
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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
Q
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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
Q
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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
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Intraparenchymal hematoma – high density mass w/ edema

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26
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Myokymic discharges – rhythmic & can be seen as singlets or multiplets; sometimes assoc w/ K+ channel antibodies

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27
Q
A

Metachromatic leukodystrophy (MLD)

*white matter demyelination w/ spared U-fibers! Confluent periventricular demyelination

also can be adrenoleukodystrophy & Krabbe’s

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28
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Agenesis of corpus callosum

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29
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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

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30
Q
A

A-comm artery aneurysm

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31
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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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32
Q
A

Non-communicating/obstructive hydrocephalus

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33
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34
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Thrombus in Vein of Galen & Straight sinus – abnormal hyperintensity on T1 & axial proton density images; hemorrhagic infarction in B thalami

35
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B frontal contusions w/ slight orange tinge 2ndary to presence of residual hemosiderin-laden macrophages

36
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A

Lacunar infarcts

37
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A

Oligodendrogliomas

38
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A

Reversible posterior leukoencephalopathy – found in pts w/ malignant HTN

Found in 85% of patients studied w/in 72 hrs after onset of sx

39
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A

Spinal stenosis - Constricted spinal canal 2ndary to degenerative facet joint disease

*no disc herniation or synovial cyst present

40
Q
A

Herniated disc

41
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A

Myxopapillary ependymoma

42
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A

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
Q
A

Communicating hydrocephalus

44
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A

Discitis

-pt had documented E. faecalis osteomyelitis affecting L2/L3; ring enhancing

45
Q
A

Wernicke’s encephalopathy / thiamine deficiency; mammillary bodies congested & discolored

46
Q
A

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
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A

Lambert eaton syndrome – incremental response cof CMAP of > 200% following exercise w/ or w/o decrement on repetitive stimulation

48
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A

Creutzfeldt astrocyte – multiple small nuclei (micronuclei) & abundant eosinophilic cytoplasm

*seen in demyelinating disease

49
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A

Germinoma – most common pineal region tumor

50
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A

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
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A

Carbon Monoxide poisoning

52
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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

53
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A

Leptomeningeal melanocytes

54
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A

DNET Dysembryoplastic neuroepithelial tumor

55
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A

Suppurative ventriculitis – abnormal ependymal enhancement & CSF hyperdense, white matter w/ marked edema

56
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A

MS

57
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A

meningothelial (arachnoid) cell cluster in the fibrovascular stroma of choroid plexus

-> occasionally give rise to meningiomas (intraventricularly)

58
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A

Pleomorphic xanthoastrocytoma – large cyst w/ mural nodule;

  • usually found in temporal or parietal lobes
  • Surrounded w/ minimal hemosiderin rim
59
Q
A

Vein of galen aneurysm – congenital anomaly

60
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A

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

61
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A

Neurofibroma or meningioma -> surgical removal

Do not need to do CT myelogram

*intradural extramedullary

62
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A

Subacute hemorrhage 2ndary to infarct (not AVM b/c it would have been bigger)

*high signal on T1

63
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A

Locus ceruleus – source of NE projections

64
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A

Pornecephalic cyst – lesion partially covered by arachnoid & extends from SAS to ventricular system; smooth walled & surrounded by abnormal radially oriented gyri

65
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A

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

66
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A

Chronic HSV encephalitis

Encephalomalacia in both temporal lobes; can have cystic changes

Hyperintensity in temporal lobes

67
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A

Neurofibrally tangle – intraneuronal intracytoplasmic inclusion composed of paired helical filaments

AD, PD, PSP, Down’s, PD complex of Guam, post-encephalitic Parkinsonism

68
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A

SDH – no need for further testing à craniotomy now!

69
Q
A

MS plaques – focal demyelination

Not epyndemoma à you’d see focal mass w/ cord enlargement

70
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A

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

71
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A
  • *Centrotemporal spikes** -
  • *Benign rolandic epilepsy of childhood;** clonic movements of face & hand that often progress to more generalized seizure
72
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A

Proximal internal carotid artery has a rounded stump w/ no distal flow

-> occlusion b/c of atherosclerosis

73
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A

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).

74
Q
A

Meningioma – intradural, extramedullary

*ependymoma, astrocytoma & hemangioblastomas – intramedullary lesions

75
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A

Arachnoid cyst – (lesion @ tip of L temporal lobe) -> spares cortical ribbon & extraaxial -> r/o head trauma or HSV; the lesion looks like CSF

76
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A

Dandy Walker Malformation – no vermis , 4th ventricle connects w/ cisterna magna, posterior fossa enlarged

77
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A

Ependymoma – perivascular pseudorosettes

78
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A

Onset latency in sensory nerve action potential; initial positivity is the AP passing beneath the active recording electrode

79
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A

Jitter on single fiber EMG -> disease in neuromuscular transmission (MG) & denervating neuropathy (ALS) ;

80
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A

Cervical portion of carotid -> C – petrosal segment of carotid artery -> cavernous portion

A – P-comm

B – distal ICA

D – ACA

E – A-comm

81
Q
A

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