By Ken HuiYee for PBL group 7
Case 24
Causes:
Thrombosis & Embolism (65% of strokes)
▪ Artery-to-artery
▪ Cardioembolic
▪ Thrombosis in-situ
Small vessel (lacunar) strokes (20% of strokes)
▪ atherothrombotic or lipohyalinotic occlusion of a small intracranial artery
▪ Often symptomless
Thrombus formation on atherosclerotic plaques embolize to intracranial arteries
▪ Carotid bifurcation
▪ most common site (10% of ischaemic strokes)
Diseased vessel may acutely thrombose
▪ Including aortic arch, common carotid, internal carotid, vertebral, and basilar a.
Arrhythmias
AF
Mural thrombus
DCM
Valvular lesions
Mitral stenosis, Endocarditis, Rheumatic fever
Paradoxical embolus
Atrial septal defect, Patent foramen ovale, Atrial septal aneurysm
Venous sinus thrombosis
Complication of:
▪ OCP
▪ Pregnancy & the postpartum period
▪ Inflammatory bowel disease
▪ Intracranial infections (meningitis)
▪ Dehydration
Less common (only 15% of all strokes)
Higher mortality rate than Ischaemic
Causes:
Head trauma
▪ Most common cause of SAH
Hypertensive haemorrhage
Aneurysm
Spontaneous rupture of small penetrating artery
Common sites:
Basal ganglia (especially the putamen), thalamus, cerebellum, and pons.
SAH from berry aneurysm
▪ AcomA, PcomA, MCA (locations from most common to less common)
Mycotic aneurysm
▪ Eg. Endocarditis
Amyloid angiopathy
▪ Degen of intracranial vessels
▪ Rare in <60
Tumour
Drugs (eg. Cocaine)
▪ Young pts
Can’t be distinguished on basis of the history or clinical examination
Ischaemic stroke tends to be painless
However h/a may still occur
Haemorrhagic stroke causes h/a esp. If ICP is raised
Investigations:
Determine between ischaemic and haemorrhagic
CT
MRI
CSF
Acute
Sudden onset
Abrupt neurological deficit
Stuttering
More likely to be thrombotic and lacunar onset
Neurological deficits wax and wane
Proceeds towards complete neurological deficits
HOPC:
▪ Pt describes a shade or curtain being pulled over the front of the eye (right)
▪ Vision in right eye is lost only for a short time (seconds to minutes)
▪ On examination patient has carotid bruits
▪ Painless
Ddx:
Amaurosis Fugax
▪ Central retinal artery occlusion
Retinal migraine
▪ Develops more slowly (15 to 20mins)
Rise in ICP
▪ Can compromise optic disc perfusion
HOPC:
▪ Sudden onset of headache with aura
▪ Nausea and vomiting
▪ Tingling, numbness and vague weakness on the right side of the body
▪ Patient prefers a dark room
▪ Patient reports that the aura has persisted for more than a week.
IX:
▪ CT and MRI show focal ischaemia
Rare complication of migraines
Definition:
Aura and a migraine headache, with the aura symptom persisting > 7/7
+ neuroimaging focal ischaemia
Complete
Total area of the brain supplied by an occluded vessel is damaged
Further prophylaxis Rx is pointless
Incomplete
some cellular damage
Additional tissue in the affected vascular distribution is at risk
Prophylaxis Rx is useful
Not that practical as distinction based on clinical findings can be impossible
HOPC:
A 62-year-old woman was admitted to MMC with acute onset of left-sided hemiparesis. On admission, she had left-sided hemiplegia and facial palsy with minor dysarthria
IX:
CT
▪ right MCA mainstem occlusion but no early ischemic changes
Thrombolysis commenced pt improved initially but then developed sudden decline of consciousness
Repeat CT
Ruled out ICH
MRI
New occlusion in Left MCA discovered
Underlying cause was due to cardioembolic ischaemic stroke due to AF
HOPC:
Pt presents to ED with global aphasia
Pt’s partner reports that pt is right handed
HOPC:
Pt presents to ED with right leg and foot paralysis
Sensory impairment (pain, temperature) over right lower limb
Examination of upper limb = normal
Impairment of gait
HOPC:
Pt presents with homonymous hemianopia
Has a failure to see to-and-fro movements, inability to perceive objects not centrally located
HOPC:
Pt presents with homonymous hemianopia
Has a failure to see to-and-fro movements, inability to perceive objects not centrally located
Reports peduncular hallucinosis
Midbrain – Subthalamic -Thalamic
Weber Syndrome
▪ Contralateral hemiplegia
Thalamic Dejerine-Roussy
▪ Contralateral hemisensory loss
Claude’s Syndrome
▪ Third nerve palsy Contralateral ataxia
Anton's syndrome
Bilateral infarction in the distal PCAs producing cortical blindness
Pt maybe unaware of blindness and may deny it
Balint’s syndrome
Watershed infarction between PCA and MCA
Disorder of the orderly visual scanning of the environment
Hypotension due to eg. AMI low perfusion in borderzones/junctional territories of the cerebral end arteries
Clinical Presentation:
“Man-in-the-barrel” clinical presentation
Optic ataxia
Cortical blindness
Difficulty in judging size, distance, and movement
Memory loss
Dysgraphia
81 yr old man with HT and AF on anticoagulants, right-handed
HOPC:
h/a, diaphoresis, dizziness, diplopia
Sudden onset of R arm tingling, numbness and weakness
Progressive slurred speech
Signs & Symptoms continued:
Horizontal eye movements/conjugated gaze restricted
Jaw deviation to the right
Bilateral facial weakness
▪ Difficulty wrinkling forehead or close eyes
Dysphagia
Balance issues
Cheyne-Stokes breathing
Dry oral pharynx
IX:
CT - progressive hemorrhagic stroke intrinsic to the pontine tegmentum of the brain stem , with rupture into the fourth ventricle
Clinical Feature
Hemiparesis
Sensory loss
Diplopia
Facial numbness
Facial weakness
Nystagmus & vertigo
Dysphagia & dysarthria
Structure Involved
Clinical Feature
Hemiparesis
Sensory loss
Diplopia
Facial numbness
Structure Involved
Corticospinal tracts Medial midpontine syndrome,
Medial inferior pontine syndrome
Lateral midpontine syndrome Medial lemniscus and spinothalamic tracts
Oculomotor/Adducens Medial inferior pontine syndrome
Trigeminal Lateral midpontine syndrome,
Lateral inferior pontine syndrome
Facial weakness Facial
Nystagmus & vertigo Vestibular
Dysphagia & dysarthria
Glossopharyngeal & vagus
Lateral inferior pontine syndrome
Medial inferior pontine syndrome
Medullary Syndrome
Occluded Blood Vessel
ICA
MCA
ACA
PCA
Basilar apex
Basilar artery
Vertebral artery or PICA
Superior cerebellar artery
Clinical Manifestations
Ipsilateral blindness (variable)
MCA syndrome
Contralateral hemiparesis, sensory loss (arm, face worst)
Expressive aphasia (dominant) or anosognosia and spatial disorientation (nondominant)
Contralateral inferior quadrantanopsia
Contralateral hemiparesis, sensory loss (worst in leg)
Contralateral homonymous hemianopia or superior quadrantanopia
Memory impairment
Bilateral blindness
Amnesia
Contralateral hemiparesis, sensory loss Ipsilateral bulbar or cerebellar signs
Ipsilateral loss of facial sensation, ataxia, contralateral hemiparesis, sensory loss
Gait ataxia, nausea, dizziness, headache progressing to ipsilateral hemiataxia, dysarthria, gaze paresis, contralateral hemiparesis, somnolence