NEURO Flashcards

1
Q

Features of psychogenic seizures? Which ones most sensitive?

A

Most sensitive: ictal eye closure, pelvic thrusting

Longer than 2 mins
Variable motor activity; waxing/waning
Vocalisation
Rapidly awake and reoriented
Twitching all 4 limbs
No prolactin rise
Surface EEG normal

UNCOMMON
- autonomic signs
- incontinence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Limbic encephalitis? Causes: 3 categories?

A

Paraneoplastic
- NMDA: ovarian
- AMPA: breast lung thymoma
- GABA: SCLC
- LGI1: SCLC, thymoma
- CV2/CRMP5: SCLC, thymoma
- Hu: SCLC
- Anti-Ma2: testicular
- GAD: SCLC, thymoma

Infection
- HSV
- VZV
- HHV

AI
- check for oligoclonal bands

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Limbic encephalitis imaging findings?

A

Temporal lobe/ limbic/hippocampal changes

T2 FLAIR hyperintensities

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

ACA stroke features

A

Dear motivation
Limb apraxia
LL > UL
Incontinence: faecal/urinary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

MCA superior stroke features

A

Broca
Temporal vision loss, opposite side
UL > LL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

MCA inferior stroke features

A

Wernicke
Parietal vision, opp side

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

MCA dominant side stroke features

A

Gerstmann Syndrome

Agraphia: can’t write
Acalculia: can’t calculate
Finger agnosia
L-R disorientation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

MCA non-dominant side stroke features

A

Contralateral neglect
Hemianopia
Hemiparesis
Constructional aprexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Posterior communicating artery stroke features

A

CN III palsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

PCA stroke features

A

CN III, IV
Vision: homonymous hemianopia with macular sparing
Alexia: can’t read but can write

Weber
- CNIII
- hemiplegia contralateral

Clause
- CNIIII
- contralateral ataxia and sensory loss

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Lenticular/subcortical stroke features

A

Pure motor MOST COMMON
Pure sensory
Sensorimotor
Hemiballismus
Dysarthria-clumsy hand syndrome
Ataxic hemiparesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Basilar stroke features

A

LOC

Locked in syndrome

Medial pontine syndrome
- CN VI, VII
- contralateral hemiparesis and sensation loss

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

AICA stroke features

A

Lateral pontine syndrome
- V, VII, VIII ipsi
- Ipsi horners
- Ipsi cerebellar
- Contralateral pain/temp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

PICA stroke features

A

Lateral medullary syndrome
- IX, X, XI ipsi
- Ipsi horners
- Ipsi cerebellar
- Contralateral pain/temp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Anterior spinal a stroke features

A

Medial medullary syndrome
- XII ipsi
- contralateral hemiparesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Carotid stroke features
- internal
- common

A

ICA
- amaurosis fugax
- ipsi dysphagia, tongue deviation
- CL vision/ sensory/ weakness

CCA
- Horner
- MCA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Carpel tunnel vs proximal median n lesion?

A

Proximal
- hypothenar, proximal thenar, dorsal of hypothenar numbness
- flexor weakness

Carpel tunnel
- pain/paraesthesia
- numbness on palm under 2/3/4th funger
- proximal thenar sensation PRESERVED

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Ulnar nerve: elbow vs wrist lesion

A

WRIST
- sensation fibres don’t pass through guyon canal
- weakness ONLY

Elbow
- weakness and paraesthesiae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Difference between common peroneal/ L5/S1 neuropathy?

A

Check notes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Difference between radial n and C7 palsy

A

Check notes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

PRRF lesion on (R) –> manifestations?

A

Can’t abduct (R) eye and adduct (L) eye

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

MLF lesion on (R)

A

Can’t adduct (R) eye
(L) eye nystagmus

INO

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

FEF lesion on (L)

A

Can’t look to the (R)
- drift slowly to (L)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

How to differentiate MS/NMO/MOG

A

Check notes: non compressive myelopathy table

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Nystagmus: peripheral vs central?
Peripheral - torsional - direction depends on canal (post = up, mid = horizontal, anterior=down) - away from lesion Central - pure vertical - toward lesion
26
Head impulse; how to differentiate central vs peripeheral?
Normal = Stroke Abnormal = Peripheral
27
Migraine pathophysiology?
CNS dysfunction --> cortical depression spreads --> irritates trigeminal --> CGRP release --> meninges irritated --> Chemicals - 5HT - GABA - Glutamate - DA
28
Features of migraine headache?
Unilateral Photophobia Phonophobia Throbbing Aggravated by movement Lasts 4-72 hours Moderate intensity N+V
29
Migraine treatment
ACUTE - 5HT (CI CVS NVS disease) - NSAIDs/paracetamol/aspirin - DA antagonists - MAB against CRGP PROPHYLAXIS - SSRIs (pztoifen) - CCB/BB - TCA - Anticonvulsants
30
Tardive dyskinesia/ drug induced Parkinsonism commonly assoc with? Treatment?
Antispychotics Benztropine, Tetrabenazine
31
Hemiballismus assoc with:
Huntingtons Basilar stroke Lesions of Subthalamic nucleus, basal ganglia
32
Tourettes: associations and treatment
ADHD: Clonidine OCD: SSRI Habit reversal training Risperdone Tetrabenezine
33
Dystonia treatment?
Levodopa Clonaz Botox
34
RLS causes and treatment
Fe def Low DA TX - opioids - dopamine agonists - Fe replacement - gabapentin, pregabalin
35
How would latent and active TB be differentiated on testing?
Active: TST, IGRA, culture (+) Latent: TST, IGRA (+)
36
Treatment for latent TB?
Monotherapy - rifamp 4 months - isoniazid 9 months - rifapentine 3 months
37
When would you treat latent TB?
Immunocomp Recent negative --> positive Young HCW Recent exposure
38
How to treat TB meningitis?
Moxiflox: penetrates meninges Dex: reduces mortality
39
How to treat TB in pregnancy?
Same: most safe
40
MDR TB options?
Moxiflox/ levoflox Mero Amikacin Linezolid Bedaquiline Cycloserine Clofazimine Pyrazinimide Delamanid Ethionamide p-aminosalicylic acid
41
Risk factors for TB infection?
Acquired immunodeficiency = MOST POTENT HIV Transplantation Renal failure Length of exposure Infectiousness of contact Smear positive Transplant
42
How to diagnose TB?
Smear/culture/ microscopy/ PCR Tissue, sputum, pleural fluid, CSF
43
What is IGRA used for? What is the significance?
Evidence of past exposure Detects T cell producing IFN-gamma to TB antigens - false negative in immunocompromised - can be active/latent/past/reinfection
44
Which genetic diagnosis associated with aortic coarctation?
Turners
45
Which immunosuppressed states are at highest risk of PJP?
Steroids Lymphopenia TNF-alpha Transplant
46
Tests for aspergillus?
Serum galactomann PCG Aspergillus precipitans
47
Management of C diff? - first episode - second episode - third episode - severe
1st: vanc/metro 2nd: vanc/fidoxamicin 3rd: FMT (comp --> bowel perd) Severe: IV metro or PO vanc
48
When do you repeat stool culture for C diff?
If symptomatic If asymptomatic, remains (+) for > 1 month so means nothing
49
What drugs frequently cause C diff?
Clindamycin 2nd/3rd cephalosporins Fluoroquinolones Amoxicillin/ Ampicillin
50
ACA features?
Motor and/or sensory deficit (leg > face, arm) Limb apraxia - Inability to perform coordinated movements Urinary/faecal incontinence Decr motivation
51
MCA features? Dominant and non dominant? Superior and inferior?
Face/ arm > leg: motor and sensory deficit Ipsilateral gaze deviation Wernicke's - IF DOMINANT inferior - Wernicke's (receptive) aphasia if in dominant hemisphere: impaired ability to comprehend speech Broca's - IF DOMINANT superior - Expressive aphasia Optic radiations - Contralateral homonymous hemianopia Non dominant parietal lobe (R) - Contralateral spatial Neglect, hemianopia, hemiparesis, constructional apraxia (difficulty with dressing) Dominant parietal lobe (ANGULAR GYRUS) --> GERSTMANN SYNDROME (L) - Agraphia: deficiency in ability to write - Dyscalculia: def comprehending mathematics - Finger agnosia: inability to distinguish fingers on hand - L-R disorientation
52
Posterior community artery stroke?
CN III
53
PCA stroke?
CNII Contralateral hemiparesis/ataxia Homonomynous hemianopia with macular sparing Alexia WITHOUT agraphia Hallucinations
54
Penetrating vessel stroke?
Pure motor Pure sensory Hemiballismus Ataxic hemiparesis Dysarthria-clumsy hand Sensorimotor
55
Basilar artery stroke?
Medial pontine Decr consc CN VI VII
56
AICA stroke?
Lateral pontine CN V VII VII Horners Ipsi cerebella Contra sensation
57
PICA stroke?
Lateral medullary CN IX X XI Horners Ipsi cerebella Contra sensation
58
Anterior spinal a stroke?
CN XII Contralateral weakness + sensation loss
59
What causes the pupil to constrict?
CNIII Parasympathetics
60
What causes the pupil to dilate?
Sympathetics --> long ciliary nerve
61
Pathway from CNII to CNIII?
CNII --> Edinger Westphal (part of OM nucleus) --> CNIII
62
Nerves in cavernous sinus?
II IV V VI
63
Physiology behind Horner's
Travels from: Hypothalamus --> pons --> C8 --> T2 Crosses over to sympathetic trunk --> up towards lung apex + bifurcation of common carotid Follows ICA --> cavernous sinus --> innervates iris and Mullers muscle
64
Causes of Horners at each synapse?
1st neuron: (hypothalamus/pons/brainstem/spinal cord) lateral medullary syndrome, spinal cord lesion above T1, pontine haemorrhage 2nd neuron: (sympathetic trunk to neck) Pancoast tumour, tumour involvement thoracic outlet/ spinal cord/ lung apex 3rd neuron: (bifurcation of CC --> cavernous sinus --> eye) ICA dissection / cavernous carotid aneurysm, neck mass, otitis media
65
Essential tremor treatment?
Propanolol - 1st line Primedone Clonaz Gaba/barbituates
66
Neutrotransmitters: receptors + action SEROTONIN
* GI ○ Entochromoaffin cells -> regulate intestinal motility * CNS (limbic system) ○ Mood ○ Appetite ○ Sleep ○ N+V ○ Arousal * Vascular ○ Stored in platelets -> released when platelets bind to a clot -> regulate haemostasis + blood clotting Inhibits release of noradrenaline
67
Neutrotransmitters: receptors + action ACh
Nicotinic Muscarinic - Neuromuscular junction * Removed by acetylcholinesterase ANS - sympathetic and parasympathetic
68
Neutrotransmitters: receptors + action Glutamate
NMDA Kainate AMPA - Main neurotransmitter in brain/spinal cord
69
PE treatment?
* Provoked (surgery, hospitalisation with immobilisation, estrogen therapy, postpartum) ○ Distal + transient risk factor: 6 weeks ○ Proximal + Transient risk factor: 3 months ○ Permanent risk factor: indefinite * Unprovoked 3-6 months * Submassive 6-12 months * Massive - indefinite
70
DVT treatment
- Distal DVT provoking factor no longer present - 6 weeks - Proximal DVT, provoking factor no longer present - 3 months - Unprovoked distal DVT - 3 months Continue therapy after 3 months if Multiple prior unprovoked episodes of DVT/PE
71
CN control of blinking:
CN V CN VII
72
Bell's palsy: how to differentiate
Central Spares eyelid and forehead muscles CANT SOMETIMES be due to peripheral cause Peripheral RARELY CAN spare eyelid and forehead muscles if distal peripheral cause Upper and low facial weakness - Inability to close eye - Drooping corner of mouth - Disappearance basolabial fold - Eyebrow sagging Impairment in volitonal movements of facial muscles Impaired in emotional expression Ipsilateral impaired taste Decreased tearing/salivation Ear pain
73
Cavernous sinus syndrome features:
3rd,4th, sixth Trigeminal neuropathy: V1 and sometimes V2
74
Cerebellopontine syndrome features:
Vestibular schwannoma, - Junction between pons + cerebellum - Lateral cranial nerves ○ V, VI, VIII
75
Superior orbital fissure lesion
III, IV, first division V, VI Invasive tumors of sphenoid bone; aneurysms
76
Brain death definition
Complete + irreversible cessation of brain function (permanent absence of cerebral and brainstem function) + Preservation of cardiac activity + maintenance of respiratory/somatic function artificially
77
Brain death criteria
(1) Widespread cortical destruction reflected by - Deep coma - No brain- originating motor response to all forms of stimulation - Pain - Seizures - Posturing (2) Global brainstem damage Absent pupillary light reaction Midposition/dilated 4-9mm Loss of corneal reflexes Loss of oculocephalic reflex Oculocephalic (Doll's eye): moving head + neck --> eyes turn with movement Loss of vestibuloocular reflex Vestibulo=ocular (caloric testing): put ice water in wear --> absence of eyes turning to irrigated side Loss of jaw jerk Loss of gag reflex Absent cough with tracheal suctioning Absent sucking/rooting reflexes Complete + irreversible apnea
78
Brain death IX
Cerebral angiography: gold standard EEG Transcranial doppler MRA with agolinium CTA
79
Drug induced parkinsonism signs + tx
Tardive dyskinesia Dystonia Akathisia Tx: Benztropine
80
Dystonia treatment
Levodopa Clonaz Botox DBS
81
Changes of hormones during sleep: what increases and decreases? Prolactin GH TSH Cortisol Urine Body
- Prolactin secretion increases - GH secretion enhanced LOW ○ Cortisol + thyroprotin inhibited ○ Urine production ○ Body temp
82
Components of sleep wake cycle?
Circadian timing ○ Driven by suprachiasmatic nuclei of hypothalamus ○ Imposes 24 hour rhythms onto a wide range of behaviours, including sleep Pineal gland ○ Synthesises + secretes melatonin into blood + CSF SCN ○ Has 2 melatonin receptors Promotes sleepiness; helps synchronise light-dark cycle (exposure to light = wakefulness) Neurotransmitters - GABA, histamine : inhibitory - Orexin - NE - Serotonin
83
Cerebellar: midline vs hemispheric signs/symptoms
MIDLINE Imbalance: Truncal ataxia: swaying of head when patient is sitting Titubation: involuntary rhythmic nodding of head/neck/trunk LL dysmetria Saccadic intrusions Nystagmus Vertigo HEMISPHEREIC Dysfidokinesia Dysmetria UL Limb ataxia Intention tremor Dysarthria Broken pursuits
84
Genes assoc with ALS/FTD
○ SOD1 mutation ○ TDP43 inclusions ○ Chr 21 ○ C9ORF72 --> linked with ALS/FTD Increased CSF glutamate = excitotoxicity theory
85
ALS features?
Upper and motor neuron weakness NO SENSORY Cognitive: FTD Flail Limb Split hand syndrome
86
ALS treatment
Riluzole Glutamate release blocker Mutlidiscplinary care improves survival NIV: improved survival, improved QOL Symptomatic therapy § Spasticity: baclofen, botox § Sialorrhea: botox, amitrytilline § Dyspnea: NIV § Weight loss/dysphagia: PEG, high protein diet
87
JVP: Describe waveform
a’ wave = atrial contraction ( a for atrial) ‘c’ wave (c for closure) ‘v’ wave (v for volume filling) ‘x’ descent = fall in atrial pressure during ventricular systole ‘y’ descent = opening of tricuspid valve
88
JVP: cases for - absent a wave - large a wave - cannon a wave - large v wave - rise in JVP during inspiration (Kussmaul's)
- absent a wave: AF - large a wave: pHTN/ pstenosis - cannon a wave: beating against closed valve --> CHB, vent arrhythmias - large v wave: TR - rise in JVP during inspiration (Kussmaul's): constrictive pericarditis
89
Medications that can trigger MG crises?
○ Aminoglycosides ○ Quinolones ○ Mg ○ BB Hydroxychloroquine
90
GBS treatment?
Ventilatory support IVIG 0.4 g/kg intravenously, daily for 5 days = NOT STEROIDS Plasma exchange
91
CIDP treatment?
IVIG CIDP responds to steroids but GBS does not Plasma exchange ○ Less preferred
92
MG medication triggers?
○ Aminoglycosides ○ Quinolones ○ Mg ○ BB ○ Hydroxychloroquine
93
MG signs? Which ones are earliest?
PRESERVED REFLEXES NO CARDIAC INVOLVEMENT Weakness - fatiguable Earliest signs - ptosis - diplopia - bulbar
94
MG antibodies + associations?
- Acetylcholine receptor Abs ○ Assoc with thymoma - Anti muscle specific kinase (MuSK) Abs ○ More likely to cause severe bulbar/ resp/ cervical weakness ○ Post synaptic - LRP4 antibodies - Stiational antibodies ○ In patients with onset < 50 ○ 95% Incr likelihood thymoma - Neuronal + titn ○ Assoc with thymoma, late onset
95
MG treatment
Mild + symptomatic: - anti-acetylcholineterases (pyridostigmine, neostigmine) Adv - steroids (NOT HIGH DOSE = WILL WORSEN) - immunosuppressants:
96
MG treatment
Mild + symptomatic: - anti-acetylcholineterases (pyridostigmine, neostigmine) Adv - steroids (NOT HIGH DOSE = WILL WORSEN) - immunosuppressants: AZA, mycoph, MTX - refractory: rites, cyclo, efgartidimod (accelerates pathogenic removal) Crises - IVIG - plasmapharesis
97
Thymemectomy indications in MG?
○ Even if hyperplasia only + < 65 years age ○ Allows you to wean ○ Can't tell if malignancy on imaging Supported by 2016 RCT --> even if MG only mild
98
Anti MUSK treatment?
More aggressive - Needs, PLEX, steroids, ritux
99
MG risk in pregnancy?
Transient neonatal MG for up to 3 months for 15%
100
Diference between LEMS and MG?
VGCC: pre synpatic No opthalmoparesis, bulbar involvement Incremental CMAP
101
Vestibular syndrome: midline vs hemispheric symptoms?
MIDLINE - Vermis, vestibulocerebellum (flocculus, nodulus), paravermis - Function ○ Motor execution ○ Rapid and slow eye movement ○ Balance/ LL coordination ○ Vestibular function - Damage causes ○ Imbalance: ○ Truncal ataxia: swaying of head when patient is sitting ○ Titubation: involuntary rhythmic nodding of head/neck/trunk ○ LL dysmetria ○ Saccadic intrusions ○ Nystagmus ○ Vertigo HEMISPHEREIC - Function ○ Motor planning, coordination of complex tasks - Damage causes ○ Ipsilateral § Dysfidokinesia § Dysmetria UL § Limb ataxia § Intention tremor § Dysarthria § Broken pursuits