Brain Tumours Flashcards

(94 cards)

1
Q

What is a tumour?

A

Swelling of a tissue

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2
Q

Classifications of brain tumours?

A

Benign OR malignant

Primary OR secondary

Supratentorial OR infratentorial

Extrinsic (AKA extra-axial) OR intrinsic (AKA intra-axial)

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3
Q

Most common extra-axial tumour?

A

Meningioma - tumours that arise from residual mesenchymal cells in the meninges; usually benign

NOTE - rarely malignant or invade brain

Produce neurological symptoms by compressing the brain

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4
Q

Other extra-axial tumours?

A

Pituitary tumours, e.g: adenoma

Cranipharyngioma

Choroid plexus papilloma

Acoustic neuroma (AKA vestibular schwannoma)

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5
Q

Occurence of primary brain tumours?

A

2nd most common tumour in children (after leukaemia)

Most common cause of cancer death <40 years

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6
Q

Presentation of brain tumours?

A

Progressive neurological deficit (main presenting feature)

Usually motor weakness

Headache

Seizures

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7
Q

Why are brain tumours not necessarily considered benign?

A

Contribute to increased mass and ICP within the rigid skull

Can also cause issues by:
• Blocking CSF flow, leading to hydrocephalus
• Haemorrhage
• Midline shift and herniations

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8
Q

Symptoms of raised ICP?

A

Headaches

Vomiting

Mental changes

Seizures

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9
Q

Types of brain herniations?

A

Subfalcine herniation (most common cerebral herniation pattern) - characterised by displacement of the brain, typically cingulate gyrus, beneath the free edge of the falx cerebri

Central herniation -
diencephalon and parts of the temporal lobes (of both cerebral hemispheres) are squeezed through a notch in the tentorium cerebelli

Uncal transtentorial herniation - a type of transtentorial herniation that occurs downwards

Tonsillar herniation - characterised by inferior descent, of the cerebellar tonsils, below the foramen magnum

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10
Q

Signs of uncal herniation?

A

Compression of CN III causes IPSILATERAL, DILATED PUPIL (parasympathetics are affected)

NOTE - this is a pre-terminal sign (patient is close to death)

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11
Q

Causes of headaches?

A

May occur with or without raised ICP, i.e: there are many causes

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12
Q

Characteristics of headaches due to brain tumours?

A

Worse in the morning (A HEADACHE THEY WAKE UP)

Headache increases with coughing / leaning forward

May be assoc. and increase in severity with vomiting

OR

Patient may have symptoms similar to tension headache / migraine (difficult to diagnose as a brain tumour)

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13
Q

Examination that must be done with headaches?

A

Fundoscopy (looking for papilloedema as a sign of raised ICP)

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14
Q

How can brain tumours cause headache?

A
  • Raised ICP
  • Invasion / compression of dura, blood vessels, periosteum
  • Secondary to diplopia (CN III, IV, VI); CN VI (false localising sign of raised ICP; they need a scan)
  • Secondary to difficulty focusing
  • Extreme hypertension (Cushing’s triad)
  • Psychogenic (stress of loss of functional capacity)
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15
Q

What is the Cushing’s triad?

A

Cushing’s reflex is a physiological NS response to raised ICP; it results in the Cushing’s triad:

  1. Increased BP
  2. Irregular breathing
  3. Bradycardia

NOTE - this is another pre-terminal event

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16
Q

In situations that are pre-terminal, what should be done about raised ICP?

A

Administer mannitol (osmotic diuretic); this works for ~20 mins, before body compensates

Organise emergency surgery

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17
Q

Define perseveration?

A

Repetition of a particular response (such as a word, phrase, or gesture) despite the absence or cessation of a stimulus

It is usually caused by a brain injury

E.g: tapping a patient at the unibrow and they continue to blink after the 1st tap (should stop blinking after the 1st), AKA Glabellar tap test

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18
Q

Define dyspraxia?

A

……….

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19
Q

Responsibilities of the frontal lobe?

A

Though, reasoning, behaviour and memory

Region for smell

Motor cortex (movement) in pre-central gyrus, anterior to the central sulcus

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20
Q

Responsibilities of the parietal lobe?

A

Intellect, thought, reasoning, memory

Region for hearing

Somatosensory cortex (sensation) in post-central gyrus, posterior to the central sulcus

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21
Q

Responsibilities of the occipital lobe?

A

Right - abstract concepts

Left - speech, motor and sensory functions

NOTE - this is for right-handed individuals

Region for vision

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22
Q

Responsibilities of the temporal lobe?

A

Behaviour
Memory
Hearing and vision pathways
Emotion

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23
Q

Mnemonic for symptoms and signs that arise due to cerebrellar issues?

A
D - dysdiadochokinesis
A - ataxia
N - nystagmus
I - intention tremor
S - scanning dysarthria
H - heel-shin test +ve
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24
Q

Indications that there should be urgent suspicion of cancer referral?

A

Focal neurological deficit - progressive deficit, inc. personality or behavioural change ((absence of previously diagnosed / suspected alternative disorders)

Change in behaviour - progressive deterioation in cognitive, psychological, behvioural and higher executive functions (absence of previously diagnosed / suspected alternative disorders)

Seizure

Headache - patients with this, vomiting and / or papilloedema

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25
Ix for brain tumours?
CT / MRI scan Lumbar puncture PET scan Lesion biopsy EEG Evoked potentials Angiograms Radionucleotide studies
26
Neuroepithelial tissues in the brain?
Astrocytes Oligodendroglial cells Ependymal cells /choroid plexus Neuronal cells Pineal cells Embryonic
27
Most common primary brain tumour?
Astrocytoma (a type of glial tumour)
28
WHO grading of astrocytomas?
I - pilocytic, pleomorphic xanthoastrocytoma, subependymal giant cell II - low-grade astrocytoma (will eventually progress to glioblastoma, if followed for long enough, i.e: ultimate behaviour is NOT BENIGN) III - anaplastic astrocytoma IV - glioblastoma multiforme NOTE - grades III and IV are malignant
29
What are grade I astrocytomas?
Truly benign ones that are slow growing; they occur in CHILDREN and young adults The posterior cranial fossa is the most common region for development Symptoms - children: • Start to walk on tip-toes • Vomiting, etc
30
Regions affected by grade I astrocytomas?
``` E.g: pilocytic astrocytomas affect: • Optic nerve • Hypothalamic gliomas • Cerebellum • Brainstem ```
31
Ix for pilocytic astrocytoma?
MRI shows strong enhancement
32
Treatment of grade I astrocytomas?
Surgery (curative)
33
Types of grade II (low grade) astrocytomas?
Fibrillary Gemistocytic Protoplasmic
34
Pathology of low grade astrocytomas?
* Hypercellularity * Pleomorphism * Vascular proliferation * Cell necrosis
35
Which regions of the brain have a predilection towards developing low grade astrocytomas?
Temporal lobe Posterior frontal lobe Anterior parietal lobe
36
Symptoms of low grade astrocytomas?
Seizures
37
Poor prognostic factors for low grade astrocytoma?
Age >50 years Focal deficit (e.g: seizures) Short duration of symptoms Raised ICP Altered consciousness Enhancement on contrast studies
38
MRI of fibrillary astrocytoma shows?
No contrast enhancement ??
39
Treatment of grade II astrocytoma?
``` Previously, all were acceptable: • No treatment; only serial imaging • Radiation • Chemotherapy • Combined radiation / chemotherapy (AKA chemoradiotherapy) - this is far more effective radiotherapy alone ``` Now the treatment is SURGERY +/- ABOVE
40
What does surgery of a grade II astrocytoma achieve?
To retrieve a biopsy sample (stereotactic vs open) Seizure control Herniation CSF obstruction Cytoreduction
41
Poor prognostic factors for surgery outcome in grade II astrocytoma?
1. Age >45 2. Low performance score 3. Large tumours (diameter >6 cm / crossing midline) 4. Incomplete resection
42
MRI appearance of anaplastic astrocytoma (grade III)?
No enhancement
43
Occurrence and prognosis of malignant astrocytomas?
Can arise de novo Median survival of 2 years
44
Occurrence and prognosis of malignant astrocytoma?
Usually it is a primary glioblastoma Median survival is <1 year
45
Spread of glioblastoma multiforme?
Spreads via white matter tracking / CSF pathways Thus, there can be multiple gliomas
46
Treatment of malignant astrocytoma?
Non-curative surgery (attempts to improve survival quality): • Cytoreduction • Reduce mass effect Post-operative radiotherapy NOTE - patients respond better to treatment if they have an MGMT methylated tumour
47
Post-operative cautions?
Not safe to drive (must inform DVLA)
48
Types of chemotherapy available?
Temozolomide PCV (Procarbazine, CCNU, vincristine) Carmustine wafers (
49
For which brain tumours i radiotherapy used for?
Low grade astrocytomas when there is: • Incomplete removal • Malignant degeneration (+/- surgery) Benign astrocytomas - only if there is recurrence / progression, not amenable to surgery, etc
50
Side effects of radiotherapy to the brain?
Drops IQ by 10 Skin and hair side effects Fatigue
51
Novel therapies towards brain tumours?
Immunotherapy
52
Occurrence of oligodendroglial tumours?
Comprise 20% of glial tumours They tend to occur in the frontal lobe Most common in adults 25-45 years but there is a smaller peak in children aged 6-12 years
53
Symptoms of oligodendroglial tumours?
Seizure presentation
54
How to differentiate oligodendroglial tumours from astrocytomas?
Calcification (typically peripheral) Cysts Peri-tumoural haemorrhage
55
Grading of oligodendroglial tumours?
* Low grade | * Anaplastic / astrocytic component
56
What are collision tumours?
Oligodendroglial cells coexist with astrocytic cells in a neoplasic collision-type tumour Possibly originate from the common precursor to oligodendrocytes and astrocytes, which are O2A cells
57
Complications of oligodendroglial tumours?
Malignant conversion
58
Treatment of oligodendroglial tumours?
Chemosensitive so: • Procabazine • Lomustine • Vincristine Surgery + chemotherapy NOTE - radiotherapy + PCV doubles survival
59
Prognosis of low grade oligodendroglial tumours?
Mean survival of 10 years
60
Symptoms to remember for brain tumours?
Headaches that wake the patient +/- vomiting New neurological deficits, inc. seizures Tip-toeing, ataxia, vomiting with headache in children
61
What are meningiomas?
Derived from arachnoid cap cells; these are extra-axial tumours Majority are histologically benign and slow-growing NOTE - in pregnancy, oestrogen causes growth; surgery is avoided, if at all possible, but sometimes must be done Some are in breast cancer patients (metastases) or in patients with NF II
62
Occurrence and symptoms of meningiomas?
Accounts for 20% of intracranial neoplasms Majority are asymptomatic
63
What is meningioma en plaque?
Represents a morphological sub-group within the meningiomas It is a carpet/sheet - like lesion that infiltrates the dura and, sometimes, invades the bone NOTE - all inv. bone should be removed to prevent recurrence
64
Types of meningiomas?
Parasaggital Convexity Sphenoid Intraventricular
65
Symptoms of meningiomas?
Headaches CN neuropathies (if at the skull base) Regional anatomical disturbance
66
Classifications of meningioma?
1. Classic 2. Angioblastic 3. Atypical (2%) 4. Malignant (5%) May occur due to metastases
67
Types of meningiomas that are the aggressors?
Clear cell, chordoid, rhabdoid, papillary (mnemonic is CRAP) Radiation-induced meningiomas (often occur following childhood leukaemia, typically in the midline)
68
CT appearance of a meningioma?
Homogenous, densely enhancing mass Oedema Hyperostosis (skull 'blistering')
69
MRI appearance of a meningioma?
Dural tail Dural sinuses are patent
70
Angiography +/- embolisation findings with a meningioma?
Occlusion of saggital sinus Angiography shows tumour blush (due to hpervascular tumour)
71
When is angiography done in a patient with suspected tumour?
Not generally indicated unless embolisation is planned
72
Treatment of meningioma?
Small meningiomas (expectant????) Pre-operative embolisation and then surgery; followed by radiotherapy
73
Recurrence of meningioma?
Depends on grade and extent of resection
74
How is extent of resection of a meningioma graded?
Simpson's grading
75
Types of nerve sheath tumour?
Schwannomas (AKA neuromas) Nueofibromas Malignant peripheral nerve sheath tumours (MPST)
76
Occurrence of acoustic neuromas?
Acoustic neuromas, AKa vestibular schwannomas (CN VIII) often occur in NF II
77
Symptoms of acoustic neuromas?
Hearing loss, tinnitus, dysequilibrium
78
Complications of acoustic neuromas?
Effect on brainstem function Hydrocephalus
79
Ix for acoustic neuroma?
Audiologic / audiometry Radiographic evaluation
80
Treatment of acoustic neuroma?
Expectant Hydrocephalus Mx Radiation NOTE - 25% are managed medically Surgery (50% are managed this way) - hearing preservation surgery rarely preserves hearing (tends to deteriorate fairly rapidly with/without tumour still being there) Gamma knife radiosurgery (25%) - if high risk or surgery refusal; it is given low dose, usually to patients with neuromas <3cm, and an MRI scan and monitoring is required afterwards
81
Complications of acoustic neuromas?
Malignant transformation is rare Hearing tends to gradually decline over several years in the treated ear Vestibular function substantially worsens in the first 6 months and then remains stable (following radiosurgery)
82
Post-operative issues with acoustic neuroma surgery?
Facial nerve palsy (damage to nerve) Corneal reflex impaired (can lead to corneal ulcers; it must be tested to ensure it is present) Nystagmus (indicates a cerebellar issue) Abnormal eye movement
83
Occurrence of germ cell tumours?
Mainly affect those <20 years, with a peak at 10-12 years More common in males than in females
84
Ix for germ cell tumours?
CT scan shows a mass that is iso- or hyper-dense Enhances Biopsy - often has mixed histology
85
Metastasis of germ cell tumours?
May metastasise via CSF
86
Types of germ cell tumours?
Germinomas - most common CNS germ cell tumour ``` Non-germinomatous: • Teratoma (mature, immature) • Yolk sac tumour • Choriocarcinoma • Embryonal carcinoma ```
87
Treatment of germ cell tumours?
Germinomas - RADIOSENSITIVE tumours (better prognosis than non-germinomatous) Non-geminomatous - less radiosensitive
88
Tumour markers?
Check the following in any child with a midline brain tumour If they are -ve, a biopsy and, potentially, a CSF sample are required
89
What do the tumour markers indicate?
They are pathognomonic and highly specific for germ cell tumours α-fetoprotein (AFP) present in yolk sac tumours and teratomas Human choriogonadotrophin (β-HCG) present in choriocarcinoma and germinoma Placental alkaline phosphatase (PLAP) present in germinoma
90
Treatment of hydrocephalus?
VP shunt (50% require a revision within 10 years)
91
Presentation of pituitary tumours?
Bitemporal hemianopia Headaches Endocrine abnormalities
92
Ix for pituitary tumours?
CHECK PROLACTIN (medially treatable with cabergoline) GH and IGF-1 for acromegaly (can be fatal due to hypertrophic cardiomyopathy) Cortisol - Cushing's disease TSH, fT4, fT3 FSH, LH (should only be high after menopause) VA and visual fields
93
Signs of panhypopituitarism?
Pallor and yellow tinge to skin Fine wrinkling of skin Absence of axillary hair Puffy, expressionless face
94
Order of loss of hormones in panhypopituitarism?
GH lost first and then LF, FSH, TSH, ACTH and, finally, prolactin