RITE Images 2003 Flashcards

1
Q
A

Axonal spheroids in diffuse axonal injury

“shear injury” -> immediately unconscious w/ trauma à chronic closed head injury

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2
Q
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Pituitary adenoma

  • Not MEGS*
  • Meningioma ependymoma glioma Schwannoma*
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3
Q

Which cranial nerve would be involved?

A

Bony erosion involving the stylomastoid foramen -> CN7 involved

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4
Q
A

Cystic astrocytoma

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5
Q
A

FTD

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6
Q
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Schwannoma of the vestibular branch of the 8th cranial nerve

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7
Q
A

14&6 Hz positive spikes best seen in referential montage

Seen in adolescents in the posterior regions during light sleep

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8
Q
A

Wilson’s

High signal intensity in Thalamus & Putamen

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9
Q
A

Cerebellar cystic hemangioblastoma

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10
Q
A

Subacute SDH w/ mass effect on ventricles -> surgery

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11
Q
A

Colloid cyst

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12
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NCS with temporal dispersion, conduction block, and slow conduction -> CIDP

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13
Q
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AVM

Can do amytal test and intravascular embolization to make surgery & radiation therapy more effective

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14
Q
A

Arachnoid cyst

Patient presents with cluster headache -> breath oxygen rich mixture if HA were to return

Do not need to drain or decompress arachnoid cyst b/c there’s no mass effect

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15
Q
A

neurosarcoidosis

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16
Q
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Congenital retinoblastoma

Pineal gland shouldn’t be calcified until age 2 -> pineoblastoma

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17
Q
A

ALS - Degeneration of the corticospinal tracts

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18
Q
A

Thrombosed superior saggital sinus

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19
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Intracranial hypotension secondary to persistent CSF leak

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20
Q
A

Epidural metastasis

Bone & inner table shows irregularity & infiltration of tumor into the epidural space (metastatic prostate CA)

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21
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Sleep spindles generated in the reticular thalamic nucleus

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22
Q
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Trichinella organism acquired by ingestion of undercooked pork

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23
Q
A

Chiari malformation w/ syringomyelia

Can get hydrocephalus due to cerebellar tonsils protruding into the foramen magnum

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24
Q
A

Cryptococcus infection

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25
No flow in basilar artery
26
Germinal matrix hemorrhage – complication of premature birth Germinal matrix = located in walls of lateral ventricles – very vascular & delicate 4 subtypes - I – localized to germinal matrix - II – ruptured into ventricle w/o ventricular dilation - III – ruptured into ventricle WITH ventricular dilation - IV – ruptured into ventricle AND cerebral parenchyma
27
2 T2 images scanned 6 months apart
abnormal signal in GP & white matter disease adjacent to trigone of R lateral ventricle; cerebral atrophy & enlarged CSF spaces; ventricular & subarachnoid spaces have increased -\> parenchymal tissue loss **Anoxic injury** in GP – If GP affected -\> CHAMWA Canavan’s & Krabbe’s – white matter lesions!
28
B symmetric, *parasagittal, cortical & BG venous infarctions* due to **thrombosis of superior sagittal sinus & deep cerebral veins**
29
**Methotrexate neurotoxicity** – multiple _PERIVENTRICULAR_ discrete or confluent **foci of necrosis** in cerebral or spinal **white matter**
30
Tethered cord syndrome – Pts w/ back pain, thickened filum terminale, widened SC, Posterior lipoma Low lying SC Axial L1/L2 should only show you filum terminale & not cord
31
**PICA infarct** – occlusion of vertebral artery
32
**Rosenthal fibers** – Alexander’s Disease
33
Onion bulbs – demyelination & remyelination Seen in: CMT CIDP Dejerine Sottas Refsum
34
Gray Matter heterotopia or heterotopic gray matter
35
Aspergillosis -\> hemorrhagic infarcts
36
**Dandy Walker Malformation** No vermis No posterior corpus callosum Large posterior fossa cyst
37
No inferior vermis & hypoplasia of 2 cerebellar hemispheres
38
Tabes Dorsalis Paraneoplastic Panel Vit E deficiency Cu deficiency
39
**Canavan’s** – U-fibers not spared
40
Colloid cyst
41
**Cryptococcus** – multiple **bubbly cysts** in **white matter, caudate, & putamen**
42
NF1
43
Subdural empyema
44
Caudate – chorea STN -\> hemiballismus SN -\> PD
45
Atrophic cerebellar vermis & loss of both Purkinje & Granule cell neurons -\> alcoholic cerebellar degeneration
46
**Clivus chordoma** – arise from embryonic notochord (mesodermal derivative) 3rd & 4th decades; extrapontine lesion Cartilaginous tumors – 20-60YO; extradural, arise adjacent to body of sphenoid bone;
47
**Hamartoma** in tuber cineureum - \*pt would have **precocious puberty**
48
Cavum septum pellucidum & cavum vergae
49
lipoma
50
ventriculitis
51
MRI is effective in demonstrating a **displaced optic chiasm** b/c it’s mo
52
Lateral Geniculate Nucleus (LGN)
53
oligodendroglioma
54
55
Cyclopia - holoprosencephaly
56
stroke
57
NPH
58
Tissue resected from intraventricular mass
**Tuberous sclerosis** abundant eosinophilic cytoplasm w/ prominent single nucleoli – **subependymal giant cell astrocytomas – SEGA!**
59
**Healed toxoplasmosis** – multiple calcified lesions seen in brain parenchyma, & cerebellum @ G/W junction – AIDS AIDS patients have generalized atrophy *Sarcoidosis – calcification is NOT a feature Sturge-Weber – intracranial calcification 2ndary to pial angiomatosis w/ curvilinear calcification following contour of cortex typically in occipital / parieto-occipital lobe* * Hyperparathyroidism – B symmetric BG calcification, dentate nuclei of cerebellum & periventricular white matter* * Tuberous sclerosis – subependymal tubers lining ventricles*
60
Flaky keratin – epidermoid/dermoid
61
Neuritic plaques!
62
**GBM!** Poorly circumscribed variegated mass w/ foci of necrosis & hemorrhage NOT infarct, abscess, meningioma or Huntington’s
63
What is disease? Clinical presentation? Treatment?
**Tolosa-Hunt syndrome** – enhancing lesion in cavernous sinus Idiopathic noncaseating granulomatous inflammation in the cavernous sinus; Acute painful ophthalmoplegia, progression over days to weeks, CN 3 & 6 involved; 4 & V1 in 1/3 Optic nerve 20%, V2 10%; may have elevated ESR & SLE; recurring attacks over months to eyars Tx: high dose prednisone
64
Small pons & cerebellar atrophy, & olive atrophy – **cerebellar pontine olivary atrophy** – look for **loss of belly of pons**!
65
Severe pontine atrophy – **olivopontocerebellar atrophy** – part of MSA; alpha synuclein
66
**Schizencephaly w/ septo optic dysplasia** – cavity lined w/ gray matter *Porencephalic cyst – cavity would be lined w/ white matter*
67
**Tumor seeding** – sagittal MR post gad who multiple round enhancing lesions on surface of spinal cord & dorsal aspect of upper thoracic cord *Cord contusions would have high signal intensity w/in the cord*
68
Hemosiderin from prior repeated SAH
69
Centronuclear myopathy Type I myofiber predominance
70
**Substantia nigra** – Damage to one SN -\> hemi parkinsonism contralateral to lesion
71
**Indusium griseum** Coronal section of CC & cingulate gyri Indusium – direct continuation of hippocampal formation
72
Thrombosed aneurysm
73
Ill defined ring enhancement w/ edema -\> **malignant brain neoplasm**
74
**Arnold Chiari Malformation** – herniation of cerebellar vermis & medulla kinking of upper cervical cord beaking of quadrigeminal plate
75
Anatomical variant of both ACA originating from LICA RPCA originates from anterior circulation – (fetal origin)
76
**Negri body** – eosinophilic intracytoplasmic inclusion in cortical neuron; seen in **rabies**
77
**Leigh’s disease** – abnormal signal in brain stem & BG symmetric -see metabolic acidosis & elevated lactate
78
**Ependymoma** – b/c tumor arises from spinal canal & molds the vertebral bodies *Chordoma – arise FROM vertebral bodies or scrum*
79
Caudate atrophy
80
**Meningioma** Non contrast CT on L -\> isointense extra-axial mass Contrast enhancement is homogeneous & intense
81
Dissection – flame shaped “stump” of ICA
82
What is E?
E – superior medullary velum thin, transparent lamina of white matter, which stretches between the superior cerebellar peduncles It forms, together with the superior cerebellar peduncle, the roof of the upper part of the fourth ventricle
83
84
**Quadrantic sectoranopia** – stroke in the LGN Anterior choroidal artery involved