Stroke syndromes Flashcards

1
Q

Cerebral vasculature
a) Branches off vertebral arteries
b) Branches off basilar artery
c) Brainstem vascular supply

A

a) PICA
b) AICA, pontine arteries, SCA, PCA
c) - Midbrain - PCA
- Pons - SCA, pontine arteries, AICA
- Medulla - PICA, vertebral arteries

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2
Q

Brainstem structures:
a) Medial (4Ms) and lateral (5 Ss) medullary structures
b) Cranial nerve nuclei

A

Medial:
- Motor pathway
- Medial lemniscus
- MLF
- Motor nerves - CN 3, 4, 6 and 12

Lateral:
- Spinothalamic
- Spinocerebellar
- Sympathetic
- Sensation for the face
- Speech/swallow nuclei - CNs IX and X (causes hoarse voice/dysphagia)

Note - signs of medial and lateral medullary signs probably indicates basilar artery pathology

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3
Q

Brainstem syndrome*
a) Lateral medullary syndrome
b) Medial medullary syndrome
c) Pontine syndromes
d) Midbrain syndrome

  • note - cranial nerve palsies generally ipsilateral to brainstem lesion
A

a) Wallenberg: occlusion of PICA, clinical features = DANVAH
- Dysphagia (PICA-chew)
- Ataxia (ipsilateral)
- Nystagmus
- Vertigo
- Anaesthesia (ipsilateral CN V palsy, contralateral pain + temp loss)
- Horner’s (ipsilateral)

b) - Contralateral limb weakness
- Ipsilateral tongue weakness/wasting and deviation to ipsilateral side (lick the lesion)
- Contralateral MEDIAL lemniscus loss (vibration, light touch, proprioception)

c) Millard-Gubler syndrome:
(paramedian artery infarct)
- Contralateral hemiparesis, ipsilateral abducens, and facial nerve palsy
- May also have dysphagia, dysarthria, conjugate gaze palsy

Locked in syndrome:
(mid-basilar* artery stroke - causing bilateral pontine infarcts)
- Corticospinal damage - quadriplegia
- Corticobulbar tract - anarthria
- Nucleus abducens - horizontal gaze palsy, but vertical gaze remains intact (as CN III/IV in the midbrain). If unilateral, could have one-and-a-half syndrome

*More distal basilar infarcts lead to subcortical/cerebellar signs but not locked in syndrome

Pontine haemorrhage will cause the above plus:
- Headache
- Pinpoint pupils
- Dolls eye reflex (nuclear gaze palsy)
- 80% die within 48 hours

d) Weber’s: - “Web in my eye”
(Paramedian branches of PCA)
- Contralateral weakness
- Ipsilateral oculomotor nerve palsy
- May have contralateral Parkinsonism if substantia nigra affected

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4
Q

What are ‘crossed’ signs

A

Brainstem lesions that cause ipsilateral features in the face (CNs) and contralateral features in the limbs

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5
Q

Moya moya syndrome
- what is it?
- who it affects?
- angiogram appearance

A
  • Vasculopathy affecting the basal ganglia, that presents with recurrent TIAs, headaches and seizures
  • Affects children 5-10 years and adults 30-50
  • Angiogram appearance - “puff of smoke”
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6
Q

Subclavian steal syndrome
a) what is it?
b) how does it present?
c) management

A

a) Stenosis of the subclavian arteries (usually due to atherosclerosis). Leads to reduction in blood flow to upper limbs, and resultant collateral supply from vertebral arteries, causing cerebral ischaemia when using arms

b) Pain/numbness in upper limbs with stroke like symptoms on using the arms (e.g. painting, dusting high surfaces, etc.)

c) antiplatelets, statins, +/- surgery

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7
Q

Carotid endarterectomy indications

A

> 50% on symptomatic side (acute non-disabling stroke or TIA)
or >80% in absence of symptoms

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8
Q

Thrombectomy
a) Indications (2, 6, 6, 24)
b) Who should undergo CT angiography?
c) Should they be thrombolysed as well?

A

a) Indications (2, 6, 6, 24):
Acute ischaemic stroke with…

Pre-stroke functional status 2 or less on the modified Rankin scale*, and

NIHSS score 6+, and

Presenting within:
- 6 hours, and confirmed large vessel occlusion** by CTA or MRA, or
- 24 hours, and confirmed large vessel occlusion demonstrated by CTA or MRA… only if there is the potential to salvage brain tissue, as shown by imaging such as CT perfusion or diffusion-weighted MRI sequences showing limited infarct core volume

*Slight disability, but independent in ADLs (do not require carers)

** LVO:
• Carotid T occlusion (internal carotid bifurcation occlusion)
• M1 (trunk of the MCA) or M2 (MCA branch in Sylvian fissure) occlusion
• Vertebro-basilar occlusion

b) Patients who fulfil the initial mRS and NIHSS criteria with likely large vessel occlusion

c) Yes, thrombolysis should be given as well unless contraindicated

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9
Q

Thrombolysis
a) indications
b) contraindications (mnemonic: ABCDEFG)

A

a) - Age >18
- Acute ischaemic stroke
- Presenting within 4.5 hours of symptom onset

b) A - AV malformation, aneurysm (or any neoplasm)
B - BP >185/110
C - CNS procedure/recent head trauma/recent stroke last 3/12
D - diathesis - active bleeding, PLT <100, INR >1.7, APTT raised on DOACs
E - endocarditis
F - former history of ICH at any time
G - glucose (hypoglycaemia)

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10
Q

Cerebellar stroke
a) Proportion of cerebellar infarcts that present with isolated vertigo
- artery affected
b) Differentiating from vestibular neuritis
c) Proportion of vertigo patients who have cerebellar stroke

A

a) 10% (and cerebellar infarcts make up 3% of all strokes)
- medial branch of the PICA

b) HINTS exam:

a) HI - catch up saccade when moving towards the affected ear (opposite to nystagmus direction) .
NT - unidirectional horizontal in VN (direction away from affected ear, worse when looking to away from affected ear). Bidirectional in CVA
Skew - vertical movement

  • Vertigo caused by cerebellar infarction tends to cause objective ataxia, whereas vestibular neuritis patients often can walk unaided
  • Vascular risk factors - previous stroke/TIA, HTN, AF, carotid stenosis
  • Focal neurology, cerebellar/brainstem signs
  • Total ipsilateral hearing loss - may indicate brainstem stroke/SOL

c) 3%

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11
Q

Timing of starting/restarting anticoagulation after acute ischaemic stroke

A

4 to 14 days post-stroke

Risk of haemorrhagic transformation highest in first 72 hours

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12
Q

TACS, PACS, PoCS and LACS

A

TACS (ACA + MCA): all 3 out of…
- Unilateral weakness/sensory deficit
- Homonymous hemianopia
- Higher cortical dysfunction

PACS: 2 out of 3 of the above

POCS: one out of…
- Palsy of ipsilateral CN, AND contralateral limb weakness, OR conjugate gaze palsy (brainstem)
- Only homonymous hemianopia (occipital)
- Cerebellar dysfunction - vertigo, nystagmus, ataxia
- Symmetrical deficit - bilateral sensory or motor deficit (brainstem)
- Reduced consciousness

LACS: one of the following…
- Pure motor stroke - unilateral weakness of face and/or arm and/or leg
- Pure sensory stroke
- Sensorimotor stroke
- Ataxic hemiparesis (combination of unilateral weakness and ataxia +/- other cerebellar signs)
- Dysarthria-clumsy hand syndrome
(note: there is no loss of higher cortical function as lacunar strokes are SUBcortical)

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13
Q

Parietal lobe syndromes
a) Dominant
b) Non-dominant
c) Bilateral occipito-parietal syndrome

A

a) Dominant = Gerstmann syndrome:
- Dysgraphia/agraphia: deficiency in the ability to write
- Dyscalculia/acalculia: difficulty in learning or comprehending mathematics
- Finger agnosia: inability to distinguish the fingers on the hand
- Left-right disorientation

https://www.youtube.com/watch?v=GLJdcmSIoNQ

b) - Hemineglect
- Spatial disorientation
- Can’t copy clock face
- Dressing apraxia
- Constructional apraxia

c) Balint syndrome:
- Optic ataxia (mis-reaching)
- Simultagnosia
- Oculomotor apraxia (can’t follow with eyes, has to turn head)

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14
Q

Barthel index
a) What does it assess?
b) 10 areas
c) Grading

A

a) Functional dependence post-stroke

b) Feeding, washing, grooming, dressing, bladder, bowels, toileting, transfers, walking on flat, stairs

c) 0-19 = totally dependent
20-39 = very dependent
40-59 = partially dependent
60-79 = minimally dependent
80+ = totally independent

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15
Q

Cortical blindness
a) Cause
b) Features o/e (including reflexes)
c) What is Anton-Babinski syndrome?

A

a) Cortical blindness is caused by bilateral occipital lobe damage (e.g. bilateral PCA infarct or basilar infarct)

b) - Total loss of visual acuity
- Normal eye movements if instructed where to look
- Normal pupillary and corneal reflexes
- Normal fundoscopy
- May be able to follow a moving object (Riddoch phenomenon) but usually not

Anton-Babinski syndrome:
- No insight into the blindness, complete denial
- Visual confabulation - will often describe in great detail what something looks like but this will be entirely fabricated
- May have visual hallucinations

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16
Q

74 year old female with sudden onset of ataxia with headache, followed by reducing consciousness
a) Diagnosis
b) Mechanism
c) Management

A

a) Acute cerebellar haemorrhage

b) Rapid expansion of SOL leading to herniation down the posterior fossa

c) Urgent neurosurgical review

17
Q

25 year old lady presents with headache, seizures, reduced GCS, left hemiparesis and extensor plantars 36 hours after delivery of a healthy baby
a) Differentials

A

a) - Venous sinus thrombosis - top differential
- Haemorrhage/stroke
- Pituitary apoplexy
- Meningo-encephalitis
- Eclampsia

18
Q

65 year old woman presents with acute left sided face and limb weakness.
Examination showed a dense left hemiparesis affecting her face (lower two-thirds), arm and leg. She had a fixed gaze palsy to the right affecting both eyes.

a) Where is the lesion?

A

a) Right frontal lobe

Note:
- Fixed gaze palsy to the right – > the eyes ‘look towards’ the side of the lesion
- Brainstem lesions would cause ipsilateral CN palsy with contralateral limb weakness, whereas here they are both on the same side, indicating a cortical lesion)

19
Q

35 year old male, involved in a 30mph car accident, presents with acute neck pain and right sided headache.
On examination, you notice a right sided Horner’s.
6 hours later, he develops a left sided hemiparesis

a) Diagnosis
b) Investigations
c) Management

A

a) Carotid artery dissection
(note - anterior stroke, vs vertebral artery dissection which will cause posterior circulation signs if any embolic event)
- Often idiopathic or traumatic; also higher risk in connective tissue diseases like EDS and Marfans

b) CT angiography

https://pmj.bmj.com/content/81/956/383

c) - If no contraindications (e.g. expanding haematoma or other bleeding risk), give antiplatelets or anticoagulation
- Consider endovascular management

20
Q

CADASIL
a) What is it?
b) Clues in the presentation
c) Associated gene abnormality

A

a) CADASIL (Cerebral Autosomal Dominant Arteriopathy with Sub-cortical Infarcts and Leukoencephalopathy) is an inherited form of cerebrovascular disease that occurs when the thickening of blood vessel walls blocks the flow of blood to the brain

b) Clues:
- Strong FHx
- Migraines
- Strokes (at a young age)
- Cognitive impairment - often have severe dementia 20 years following first symptom onset
- May have psychiatric illness

c) NOTCH-3 gene

21
Q

Vertigo
a) HINTS exam - who for? Signs for each

A

a) Only for acute vestibular syndrome with continuous vertigo & nystagmus (plus no other focal neuro deficit)

HI - catch up saccade when moving towards the affected ear (opposite to nystagmus direction) .
NT - unidirectional horizontal in VN (direction away from affected ear, worse when looking to away from affected ear). Bidirectional in CVA
Skew - vertical movement

22
Q

Cerebral venous sinus thrombosis (CVST)
a) Pathophysiology
b) Causes
c) Presentation
d) Investigations
e) Management

A

a) Thrombus formation in one of the dural sinuses. If in the cavernous sinus, referred to as cavernous sinus thrombosis.
Causes vasogenic oedema, leading to:
- Reduced cerebral arterial flow and stroke (1% of all strokes)
- Raised ICP

b) - Cavernous sinus thrombosis - usually infection, from orbital cellulitis/sinusitis
- CVST - prothrombotic states e.g. pregnancy, COCP, puerperium, malignancy, infection, trauma, inflammatory diseases, thrombophilias

c) - Headache, raised ICP features, stroke syndromes, seizures, CN palsies
- Sagittal sinus (62% cases) - hemiparesis, hemineglect, hemisensory loss, hemianopia, seizures
- Transverse sinus - aphasia if left sided, seizures
- Sigmoid sinus - mastoid pain, lower CN palsies
- Deep sinuses - altered GCS, gaze palsies
- Stroke syndromes
- CST causes retro-orbital pain, chemosis, proptosis, CN III, IV, V1, V2 and VI palsies

d) - Plain CT or MR initially to exclude stroke/SAH etc.
- Then CT or MR venography
- FBC, clotting, INR
- D-dimer - has high NPV in patients with isolated headache i.e. if negative, with normal CTB and without other risk factors, may avoid doing venogram

e) - Anticoagulation - LMWH vs UFH vs VKA vs DOAC
- Endovascular
- Surgical (if herniation, midline shift, etc.)

23
Q

Haemorrhagic transformation: risk factors

A
  • Higher NIHSS score (If >15, risk of HT is 50%)
  • Thrombolysis, thrombectomy
  • Anticoagulation (wait 4-14 days generally)
  • HTN
  • Hyperglycaemia
  • Low PLT, coagulopathy
24
Q

32 year old female with history of migraines with aura, hearing impairment and diabetes. Presents with episode of left sided face, arm and leg weakness with left hemifacial twitching. She has also had muscle weakness in legs over the past few months. UMN signs on examination. Normal fundoscopy. She has a short stature with normal BMI.
a) Likely diagnosis
b) Confirming the diagnosis
c) Treatment

A

a) Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).
This is a condition that affects many of the body’s systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy).

b) - MRI scan showing multiple cortical lesions not corresponding to specific vascular territory
- Lactic acidosis
- Mitochondrial DNA analysis

c) Scanty evidence
- Possible role of L-arginine, or vitamin supplementation

25
Q

ROSIER for rapid assessment of possible stroke in ED

A

Lose 1 point for:
- LOC
- Seizure

Gain 1 point for:
- Asymmetric facial weakness
- Asymmetric arm weakness
- Asymmetric leg weakness
- Speech disturbance
- Visual field defect

If score = 1 or more –> stroke possible
If score = 0 or less –> stroke unlikely

26
Q

Suspected TIA management
- in ED
- in TIA clinic

A

In ED…
- Give 300mg aspirin STAT unless contraindicated, then 75mg aspirin or clopidogrel daily
- All patients should have FBC, U&E, LFT, bone profile, clotting, cholesterol & lipid profile, glucose
- All patients should have an ECG
- Do not offer CT brain unless another diagnosis possible
- Refer for TIA clinic assessment within 24 hours (irrespective of ABCD2 score)
- Advise not to drive until TIA clinic review

In TIA clinic…
- Offer MR brain including DWI following TIA clinic assessment on same day as assessment
- Bilateral carotid artery ultrasound
- Holter monitor
+/- ECHO
- Continue antiplatelet 75mg OD
- Blood pressure control
- Statin
- Glycaemic control
- Advise not to drive for 1 month following symptoms (or longer if symptoms recur/not resolved)