Tumours of the Nervous System Flashcards

(44 cards)

1
Q

Supra/infra tentorial describes tumours above and below what structure in the brain?

A

Tentorium cerebelli

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2
Q

How do brain tumours usually present?

A

Neurological deficit
Motor weakness
Headache (due to raised ICP)
Seizures

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3
Q

Most brain tumours are secondary. TRUE/FALSE?

A

TRUE

Most are metastases

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4
Q

How does hydrocephalus usually present?

A

sudden raised ICP
=> headache
=> vomiting (due to vomiting centre in thalamus)
=> seizures

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5
Q

An uncal transtentorial herniation presses on which cranial nerve, causing what symptom?

A

Presses on CN III
=> prevents parasympathetics reaching pupil
=> sympathetics unopposed
=> dilated “Blown out” pupil

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6
Q

What features of a headache would make you suspicious of a raised ICP?

A

Headaches which wake the patient up

OR if it gets worse when coughing/leaning forward

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7
Q

What other symptoms are usually present with a tumour headache?

A
  • Diplopia (double vision)
  • difficulty focussing
  • extreme hypertension (cushings triad)
  • psychogenic
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8
Q

What behaviours would be affected if the frontal and/or parietal lobes were affected by a tumour?

A

Thought
Reasoning
Behaviour
Intellect

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9
Q

What would be impaired if the occipital lobe was affected by a tumour?

A

Speech

Vision

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10
Q

The referral guidelines suggest a referral after presentation of what symptoms?

A
  • behaviour change
  • seizure
  • headache
  • focal neuro deficit
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11
Q

What investigations would be carried out after a referral for a possible neurological tumour?

A

MRI
Lumbar puncture for CSF markers
Biopsy may be used, but ultimately surgeon may attempt full excision

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12
Q

Is papilloedema a late or early sign of raised ICP?

A

LATE

<10% have this on presentation with increased ICP

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13
Q

What general symptoms should be checked if suspicion of brain metastases is high?

A
  • unintentional weight loss
  • haemoptysis/haematuria
  • evidence of melanoma on skin
  • check axillae for freckling => neurofibromatosis Type 1
  • check toenails for subungual keratomas => tuberous sclerosis
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14
Q

What are the 4 grades of nervous system tumours set out by the WHO?

A

I - benign
II - pre-malignant (can change over years)
III - malignant
IV - aggressively malignant

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15
Q

Where and in what what patient groups are Grade 1 astocytomas normally found?

A

Cerebellar/ brainstem tumours

found in children and young adults

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16
Q

How quickly do grade 1 astrocytomas grow, and how are they treated?

A
Grow slowly (benign)
Tx: surgical excision
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17
Q

Grade 1 astrocytomas take up contrast on CT. TRUE/FALSE?

A

TRUE

Look like meningiomas on CT

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18
Q

Where do low grade astrocytomas (Grade II) present and what symptoms are usually experienced?

A

Temporal lobe
Anterior parietal/posterior frontal lobes

  • present with seizures
19
Q

DO grade II astrocytomas take up contrast?

A

No

Look well circumscribed BUT difficult to see exact margins

20
Q

Grade II astrocytomas can progress to grade III or IV. TRUE/FALSE?

21
Q

What indicates a poor prognosis?

A

> 50 years old

  • focal deficit
  • short symptom duration
  • raised ICP
  • altered conciousness
  • enhances with contrast (both grade III and IV do this)
22
Q

When would it be unsafe to excise a tumour?

A

If it is in an area of the pons/brainstem where removal would cause significant damage

23
Q

What genetic co-deletion increases chance of survival post-resection?

A

IDH-1 1p19q co-deletion

24
Q

Radiotherapy and chemotherapy in combination after surgery have imporved life expectancy. TRUE/FALSE?

25
What is the average life expectancy for a patient diagnosed with grade IV glioblastoma?
14 months
26
What substance is used to highlight tumour outlines during surgery?
5-ALA Protoporphyrin 9 (patients drink this prior) | When illuminated with blue light = pink
27
Patients who have surgery to excise a glioma are not allowed to drive afterwards. Why is this?
Seizure risk | OR visual field defect
28
What oral chemotherapy agent is sometimes used after surgery?
Temozolomide
29
Where do oligodendroglial tumours (grade II) usually arise and in which patient group are they most common?
Frontal lobe | 25-45 years old
30
What is used to treat oligodendroglial tumours (grade II) ?
PCV (procarbazine, lomustine and vincristine) | - as they are chemosensitive
31
What symptoms in a child would make you consider a posterior tumour?
Tiptoeing OR ataxic gait vomiting headache
32
Who should all neurooncology patients be referred to?
Macmillan nurses
33
What is psychomotor retardation?
Patients lose capacity as a result of their tumour and become apathetic
34
Meningiomas are mainly asymptomatic. TRUE/FALSE?
TRUE
35
Females are more likely to get meningiomas than males. TRUE/FALSE?
TRUE (3:2)
36
What can patients with meningiomas possibly present with?
CN palsies | headache
37
What are the types of aggressive meningiomas?
Clear cell Chordoid Rhabdoid Papillary **likely to recur and need second surgery**
38
Why do frontal lobe tumours in the elderly present late?
Symptoms overlap with cognitive decline of elderly anyway
39
How are meningiomas treated?
Small => leave alone | Larger => surgery (esp. if neuro deficit)
40
When is complex surgery for acoustic neuromas used?
If 4th ventricle has become blocked off => causing hydrocephalus
41
How many hydrocephalus shunts stop working after 10 years?
50%
42
What side effects can occur after an operation to excise a tumour?
facial nerve palsy corneal reflex nystagmus
43
What symptoms are present in a pineal tumour?
- nystagmus - weak upwards gaze - eyes bulge forward as extra-ocular muscles are compressed - hydrocephalus
44
What tumour markers are important in nervous system tumours?
Alpha-feto protein HCG LDH **if these are negative - do biopsy**