Imaging SBAs Unit 6 Flashcards

(33 cards)

1
Q

Child, Cerebellar mass, extending into cerebellopontine angle. Intense enhancement and diffusion restriction with surrounding oedema

A

Atypical teratoid/rhabdoid

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2
Q

Primary CNS Lymphoma vs Toxoplasmosis

A

CNS:
Usually single lesion,
Subependymal spread,
Solid enhancement pattern
Toxoplasmosis:
Multiple lesions
Usually basal ganglia
Ring enhancement

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3
Q

Most posterosuperior ethmoid air cell, separated from optic nerve and ICA by very thin bone

A

Onodi cell

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4
Q

Most anterior ethmoidal air cell

A

Agger Nasi cell

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5
Q

Enhancing mass at base of tongue in midline

A

Lingual thyroid

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6
Q

Definitive Ix for herpes encephalitis

A

Lumbar puncture

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7
Q

Carotid body tumour MRI

A

Iso T1, High T2, multiple flow voids

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8
Q

Causes of high T1 in basal ganlgia

A

Calcification,
Haemorrhage, Wilsons, Long term TPN,
Chronic liver disease,
NF1 hamartomas

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9
Q

MIR signs of malignant transformation of pleomorphic adenoma

A

Heterogenous signal,
Irregular margins,
Lymphadenopathy,
adjacent soft tissue or bone spread,
Facial perineural spread

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10
Q

Pleomorphic adenoma MRI

A

Low T1, High T2.

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11
Q

Causes of visual field defects

A

Temporal lobe = contralateral superior quadrantinopia
Visual cortex = contralateral homonymous hemianopia
Occipital lobe = homonomous hemianopia with macula sparing
Optic chiasm = bitemporal hemianopia
Optic nerve = ipsilateral anopsia

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12
Q

Renal impairment, hypertension, intracranial aneurysm

A

ADPKD

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13
Q

Acute carbon monoxide poisoning MRI

A

High T2 signal in basal ganglia and globus pallidus with diffusion restriction

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14
Q

Multiple rounded cystic intracranial lesions, surrounding oedema, immunosuppressed.

A

Toxoplasmosis

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15
Q

Von-Hippel-Lindau associations

A

Cerebellar haemangioblastoma,
Spinal cord haemangioblastoma,
Retinal Haemangioblastoma,
Pancreatic cysts,
Renal cysts,
RCC,

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16
Q

Causes of basal ganglia calcification

A

Toxic (CO, Pb, radiation, chemo),
Infection (Torch),
Metabolic (hypothyroid, hypoparathyroid, pseudohypooparathyroid, hyperparathyroid)

17
Q

Laryngoceles are associated with

A

Laryngeal Cancer

18
Q

Intermittent cyanosis on crying in neonate (Dx and Ix)

A

Bilateral choanal atresia,
CT nasal passage

19
Q

Swelling and high signal in hippocampi and amygdala.
Poor memory, hyponatraemia, seizures

A

Limbic encephalitis, often paraneoplastic

20
Q

Sturge Weber caused by

A

Cortical venous angioma with gradual calcification

21
Q

Heterogenous cystic mass with solid enhancing components and calcification - Suprasellar

A

craniopharyngioma

22
Q

NF1 diagnostic criteria

A

2 or more of the following:
6 cafe-au-lait spots during 1 year.
2 or more neurofibromas or one plexiform neurofibroma
optic nerve glioma
distinctive osseous lesion
sphenoid wing dysplasia
2 or more Lisch nodules
Axillary or inguinal freckling
Primary relative wit NF1

23
Q

Risk factors for future haemorrage in brain AVM

A

Intranidal aneurysms,
Venous ectasia,
Posterior fossa location,
Previous haemorrhage

24
Q

Epidermoid cyst vs arachnoid cyst

A

Epidermoid demonstrate diffusion restriction

25
Base of infundibulum lesion, isointense to brain on all images
Hypothalamic hamartoma/Tuber cinereum hamartoma
26
Cortical lesion, central high intensity on T1/T2 with low T2 rim
Cavernoma
27
Normal cranial suture width for 2YO
<1mm
28
Metabolic storage disease associated with
Macrocephaly
29
J shaped sella
Flattened tuberculum sellae, caused by: Normal variant, Optic chiasm glioma, NF, Achondroplasia, Mucopolysaccharidoses, Chronic hydrocephalus
30
Orbital pseudotumour
Low T1 and T2 signal in occular muscle, sparing tendons
31
Floating teeth causes
No obvious supporting bone for teeth. Seen in: Severe peridontal disease, LCH, Hyperparathyroidism, Mets & myeloma
32
Frontal sinuses mucosal disease caused by obstruction at
Anterior hiatus semilunaris
33
Contents of jugular foramen
Pars nervosa: Inferior petrosal sinus, Glossopharyngeal nerve (CN 9) Pars Vascularis: Jugular bulb, Vagus nerve (CN 10) Spinal accessory nerve (CN 11)