STROKE: Sudden loss of
neurological function
due to interruption of
blood supply
Ischaemia -
blockage of a
blood vessel (85%)
THROMBOSIS:
Stroke due to clot
which has arised
from within the
arteries of the brain
Atherosclerosis = in
the blood vessil
itself
May be caused by
blood disorders
that promote
clotting like Sickle
cell disease ,
Thrombophilia
EMBOLISM: Clot that
travels from the heart,
blocking brain
circulation
May be caused by
damaged heart
vavles, artificial
valves, disorders
of rhythm
TIA: Transient
Ischaemic Attack -
temporary and
reverseable loss of
function within 24
hours
Sometimes
known
as
'mini'
stroke
Speedy attention to
prevent major stroke
Can do doppler
ultrasound to assess
the state of arteries in
the neck may need
Endarterectomy to
open up blocked blood
vessil.
Fatal up to
30% for first
month
Haemorrhage -
rupture of
blood vessel
(15%)
Less common
Normally blood - brain
barrier separates blood
from brain. Once blood in
contact with brain tissue
quite toxic
Ischaemic
stroke tend
to survive
better
fatal in up to 50%
of victims in the
first month
SYMPTOMS - weakness arm or
leg, sensory
impairment, visual
on one side…
RISK
FACTORS
Hypertension: Should be
treated as precipitates
hardening of the arteries
making them easy to
block or rupture
Diabetes and
hypertension go
hand in hand - one
cause of
hypertension is renal
/ kidney cause
Age
Smoking - can also
lead to can lead to
atherosclerosis
(artery hardening)
High
cholesterol -
fuzzing of
arteries
Family history /
genetic
pre-disposition
Heart problems, e.g.
Atrial fibrillation :
disturbance in heart
rhythm leading to
clot
2:1000 new cases
ever year
3rd major cause of
death after cancer
and heart disease
Major cause of
disability
DIAGNOSIS
Brain CT or Brain MRI used to
image brain. MRI more
detailed but CT more readily
available.
Can have coloured scans for
the blood vessels if diagnosis
is not straight forward.
Manifestation
depends on area of
brain affected
Described as Anterior
circulation or posterior
circulation infarction
depending on whcih
affected
May be called:
severe, mild,
moderate are 3
classifications etc…
ANTERIOR circulation
infarction features (affect
opp side of body)
Hemiplegia:
weakness of
upper and
lower limbs
Hemianesthesia:
lack of sensation
Hemianopia:
Loss vision
one side field
Dysphasia: Inability
to express self or
understand others
Inattention: Unable
to pay attention to
one side of body /
environment
More able to
treat this kind of
infarct - e.g. if in
the neck
Posterior surgery
more risky and
less rewarding
POSTERIOR
circulation
infarction
Vertigo / unsteadiness
Loss of vision
/ double
vision
Upper and
lower limb
weakness
Dysarthric
speech
Receptive
dyspasia
ACUTE STROKE MANAGEMENT
1. Confirm diagnosis of stroke
2. Confirm whether ischaemic or haemorhaggic
3. Maintain: airway, circulation, hydration, skin, bladder and bowel function
4. If catch them in a 4 hour window the patient may be
entitled to Thrombolysis – has to be ischaemic not
heamorrhagic- give them a drip to dissolve a clot. (About 20%)
4. If haemorrhage is
superficial chance you can
take the clot out, reduce
pressure in the skull '
surgical evacuation'
e.g. young people
with deteriorating
level of
consciousness or
Cerebellar
haematoma
5. Prevent complications like:
Aspiration Pneumonia / Deep
vein thrombosis which can lead
to pulmonary embolism
6. Secondary
PREVENTATIVE
TREATMENT
Anti-platelets
therapy like
Aspirin
Lipid lowering / statins
lowers further
hardening of the
arteries (as result of
cholesterol).
Full
anti-coagulation
like giving Warfarin
- have to monitor
Diabetes /
hypertension
mangement
Stop smoking
Healthier life style
Major risk of this
haemorrhage however.
1/8 full recovery. 1/17
bleeding.
4. Endarterectomy: Opening
up a narrowed artery by
surgical operation if there is
70% blockage when the pt
suffers a small stroke
Control of circulation: If
haemorrhagic keep low,
ischaemic keep high or
likely to make it worse
BRAIN TUMOUR: New growth
of cells which form lesion /
lump
BENIGN Neoplasm: Does
not infiltrate normal
tissue or metastesize
Removed with
out recurrance
Malignant Neoplasm / cancer: Has aggressive
characteristics – multiplies
rapidly, doesn’t usually have a
capsule – unlike benign
Metastasis to
other areas of
body
Recurrence after
removal
CLINICAL FEATURES
Raised ICP: If
increase by 30ml
(one tenth can of
coke) you will have
problems.
Affects on
local tissue
Headache:
Worse in
morning,
better as day
goes on
Vomiting
Bradycardia:
Slow heart
rate
Hypertension
Impairment on
concious level
Papilloedema: swelling
of the cranial nerves.
You can see the selling
of optic nerve through
the eye….
Epilepsy
WHO CLASSIFICATION
1. Tumours of
Neuro-epithelial
origin
(Gliomas)
Astrocytoma: Most
common form of
Glioma in children
and adults - develop
from astrocytes
(neurones)
High / low grade
(slow or rapid)
growth
3 Subtypes
a. Localised - less malignant
b. Diffuse - more malignant
c. Anaplastic - very bad news
Glioma = arising
from the BRAIN
TISSUE and
supporting
structures itself
Oedema around the
glioma shows
multiplying and
dying very quickly
Midline shifted left
Oligodendroglioma:
from
oligodendrocytes
that make myelin
3% of brain
tumours
Slow growing - doesn't
have such an effect on
surrounding structures
till gets big
Cerebral
hemisphere
Adults
Medulloblastoma
Most common
in childhood
Coz at base of the
brain, can block flow
of CSF.
Agressive
In Posterior
Fossa
Can be removed
2. Tumours of
cranial and
paraspinal
nerves
Vestibular
schwannomas
Arise location:
Schwann cells on VIII
cranial nerve
Slow
growing -
benign
Older people
Rarely spread
Loss of hearing
Unilateral / bilateral
Rarely associated with
Neurofibromatosis type 2
Can remove, but
risk damage to
facial nerve VII
Presses on the
cerebellar pontine angle –
dangerous to press on the
Pons – heartrate, CSF flow
etc… so needs to go.
Lack of balance
Spinal cord tumours
20% CNS
tumours
Meningiomas
Neurofibromas
Cordomas
3. Tumours
of the
meninges
Meningiomas -
25% adult
brain tumours
Older people
Arise Location :
cerebrum,
cerebellum
Meningeal tail' -
tumour blends
with meninges
4. Tumours of the
haematopoetic
system
Lymphomas
affecting brain
or spinal cord
5% CNS tumours
Arise: Diffuse
large B-cells non
Hodgkin
lymphoma
5. Tumours of
the sellar
region
Craniopharyngiomas
Rare benign tumours
Base of
brain,
close to
pituaitary
Can cause
impaired
vivsion
Children
and young
adults
Pituitary tumours
Benign
8% of tumours
Can be functioning
(release hormones) or
non - functioning
Grow slowly
Don't spread
Can affect
Thyroid &
hormone
secretions
Can effect
blood
pressure
6. Metastatic
Tumours
Colour
under
dye (like
Lymphomas)
Grades of tumour
1-4: 1 benign 2 partly
benign 3 low
malignancy 4 high
malignancy
Analysis of mitotic division
under microscope…
Histological grading =
specimin of tumour, section,
stain, and histopathologist
examine through microscope.
(Histo = tissue)
ASSESSMENT:
CT scan, MRI
Angiogram for
surgeons – to see
where blood is
coming from in the
blood vessels &
where to stop the
bleeding in advance
etc.
MANAGEMENT
Palliative like
reduction of
ICP
Surgery:
Partial or
total
excision
Anti
epilepsy
drugs
Steroids -
reduce
swelling
Grade tumour
directs what
best form of
Chemo / radio
therapy
New biologic /
targeted
therapies -
less harmful,
halt tumour
growth