CNS Flashcards

1
Q

Glioma Treatment Volumes Low and High Grade

A

low grade: 1-2cm around GTV

High grade: 2-3cm around GTV

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2
Q

Meningioma Treatment Volumes Benign and malignant

A

Benign: 1cm
Malignant: 3cm

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3
Q

Primary Spinal cord volume

A

width of post fields 7-8cm
5cm for children

1-2 vertebral bodies above and below

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4
Q

Motor speech area of the brain

sensory speech area of the brain

what is the circle of willis

A

Broca

Wernicke

Supplies blood to brain

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5
Q

Meningioma Dose

A

Unresectable or recurrent benign : 5040-54
Atypucal: 54-60
malignant: 60

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6
Q

Lymphoma dose

A

2340-3600

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7
Q

Primary Spinal cord dose

A

Intramedullary, ependymoma and astrocytoma
-5040

high grade: 54
SBRT: 10-16

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8
Q

Glioma Dose

A

RT used for post op, high grade tumours, residual disease, high risk

EBRT, sterotactic or brachy
45-60

low grade 50-54

high grade 60

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9
Q

Locations of tumours and how they affect patients

Frontal

A

Short term memory loss, episodes of falling or difficulty walking, personality changes, mood changes, moto skills, hemi-paralysis, seizure, drowsiness’, decrease attention

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10
Q

Locations of tumours and how they affect patients

Temporal

A

Loss of memory, difficulty with hearing, loss of smell, exhibiting signs of not being able to understand and comprehend directions, proptosis

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11
Q

Locations of tumours and how they affect patients

Parietal

A

Controls sensations, loss of memory, difficulty with hearing

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12
Q

Locations of tumours and how they affect patients

Occipital, Cerebellum and cerebrum

A

sudden loss of eye sight in one eye

Balance, movement, balance (ataxia)

Temperature, Unilateral weakness and mental changes

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13
Q

Glioma Pathology

A

MC are gliomas–>can start in the brain or spine

main type of glioma

  • astrocytoma
  • ependymoma
  • oligodendoglioma
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14
Q

Meningioma pathology

A

Benign (Grade I) 90%
Fibrous + transitional
Atypical (Grade II) <10%
Anaplastic/malignant (Grade III) <5%

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15
Q

Lymphomas pathology

A

Most are large diffuse B cells lymphoma
-T cell more aggressive and poorer prognosis

Common to have more than one tumour present

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16
Q

Primary Spinal Tumour

A

Mostly are benign but are problematic

  • Extramedullary
  • Intramedullary
17
Q

Prognostic indicators for:

  1. Gliomas
  2. meningioma
  3. lymphomas
  4. primary spinal cord
A
  1. High grade
  2. Location of lesion
  3. AGE!!
  4. tumour type
18
Q

Epi/Eti for

  1. Gliomas
  2. meningioma
  3. lymphomas
  4. primary spinal cord
A
  1. increase with age (40-80)
    environment + occupational factors
  2. sporadic, more common in women (benign), family history and RT to scalp
  3. immunocompromised like HIV
  4. most intramedullary are astrocytomas or ependymoma. TSpine
19
Q

S&S + MC site for

  1. Gliomas
  2. meningioma
  3. lymphomas
  4. primary spinal cord
A
  1. dependent on location
    mc location is in cerebrum (supratentorial)
    always grow back
  2. Asymptomatic-location based
    -localized headaches & seizures
    usually benign
  3. dependent on site-tumours are often deep an cause seizure
    MC location is cerebrum (supratentorial)
  4. Pain-localized to involved region
    numbness/weakness
20
Q

In general…

  1. S&S
  2. prognostic indicators
  3. Medications
  4. Dose rage
A
  1. head aches
  2. Pathology/types of tissues involved
  3. Dexamethazone/Decadrom: swelling
    Temozolomide: Radiosensitizer chemo agent
  4. 45-60Gy (200/fx)
21
Q

Spine Tx volume

A

width for post fields 7-8cm (5cm for children)
1-2 vertebrae above and below
cervical lesions 4-6MV
T+L spine 10-23MV