Neurology Flashcards

1
Q

Which medications can improve symptoms of dementia?

A

Acetylcholinesterase Inhibitors

Anti-Glutamates - Memantine

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2
Q

What is the gait of somebody with cerebellar ataxia?

A

Broad Based Gait. Stance becomes incoordinated. When walking, the person tends to veer to the side of the affected lobe. If midline structure affected, there will be a tendency to fall backwards or sideways.

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3
Q

What is the gait of somebody with sensory ataxia?

A

Stamping gait. Peripheral sensory loss causes ataxia because of loss of proprioception. a broad based high stepping gait develops as feet are placed clumsily, relying in part on vision, s obalance is worse with eyes closed?

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4
Q

What level must a lumbar puncture be performed at?

A

Between L3 and L5 - Cauda Equina

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5
Q

How does Optic Neuropathy present in MS?

A

Inflammation of the optic nerve produces blurred vision and unilateral eye pain.
A lesion in the optic nerve head produces disc swelling (optic neuritis) and pallor (optic atrophy) following the attack. When inflammation occurs in the optic nerve further away from the eye (retrobulbar neuritis) examination of the fundus is normal.

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6
Q

What is the difference between an ischaemic and a non-ischaemic stroke?

A

Ischaemic - blockages to blood vessels - Osmotic potential in certain area changes so water moves into area - swelling - area becomes darker on CT

Non Ischaemic: Bleeding - Intracranial haemorrhages (burst blood vessel) - Cerebral Amyloid …

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7
Q

Amaurosis fugax is associated with problems around which artery?

A

Ophthalmic Artery

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8
Q

What are the two main patterns of demyelination in MS?

A

Pattern I - Macrophage mediated demyelination

Pattern II Antibody mediated demyelination

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9
Q

Where does a subarachnoid haemorrhage most commonly occur?

A

Basilar artery (Berry Aneurysm)

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10
Q

Which nerve is affected in carpal tunnel syndrome, which ligament is it trapped under?

A

Median Nerve, entrapment under transverse ligament

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11
Q

What is Ménière’s disease?

A

Ménière’s disease (MD) is a disorder of the inner ear that is characterised by episodes of feeling like the world is spinning (vertigo), ringing in the ears (tinnitus), hearing loss, and a fullness in the ear.

Typically only one ear is affected, at least initially; however, over time both ears may become involved. Episodes generally last from 20 minutes to a few hours. The time between episodes varies. The hearing loss and ringing in the ears may become constant over time.

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12
Q

What is status epilepticus?

A

This is a medical emergency. There are continuous seizures for 30 minutes or longer. When grand mal seizures follow one another, there is a risk of death from cardiorespiratory failure. Precipitants include stopping treatment, alcohol abuse, intercurrent illness and poor compliance with therapy. Rectal diazepam or buccal midazolam is given out of hospital.

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13
Q

How will a patient with hemiparesis walk?

A

Stiff and weak leg is circumducted and drags

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14
Q

What are the symptoms of a subdural haemorrhage?

A

Increased Intracranial Pressure - Headache, Seizures, Vomiting

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15
Q

Where do the biggest ischaemic strokes tend to take place?

A

Middle Cerebral Artery

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16
Q

Which absent criteria define brainstem death (7)?

A
Unresponsive Pupils, Corneal Reflex, 
Caloric Vestibular Reflex, 
Cough Reflex, 
Gag Reflex, 
Respirations, 
Response to Pain
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17
Q

Where do Berry aneurysms occur?

A

At the junctions of the circle of willis.

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18
Q

What are the four characteristic features of Parkinson’s disease?

A

Tremor, Rigidity, Akinesia & Postural Changes

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19
Q

What is Romberg’s test? What could a positive result indicate?

A

In the Romberg test, the standing patient is asked to close his or her eyes. An increase loss of balance is interpreted as a positive Romberg’s test.

Positive result could indicate drug or alcohol intoxication or sensory ataxia.

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20
Q

What are the four clinical patterns of MS

A

Relapsing-remitting MS (RRMS) : This is the most common (85-90%) - symptoms occur in attacks with onset over days and typically recovery. Patients may accumulate disability over time if relapses do not recover fully.

Secondary Progressive MS : Gradually worsening disability progressing slowly over years; 75% of patients with RRMS will eventually evolve into this.

Primary Progressive MS (PPMS): (10-15%) gradually worsening disability without relapses or remissions and typically presents later and is associated with fewer inflammatory changes on MRI.

Relapsing Progressive MS: The least common form, similar to PPMS but with occasional supra-added relapses on a background of progressive disability from the outset.

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21
Q

What are the symptoms of Horners Syndrome?

A

Meiosis, Ptosis, Anhydrosis, Enopthalmos

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22
Q

Which sensory fibres transmit proprioception?

A

A Alpha

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23
Q

Which conditions could cause sensory ataxia?

A

Vitamin deficiencies such as Vitamin B12

Conditions affecting the dorsal columns of the spinal cord, such as tabes dorsalis (neurosyphilis), in which it was first described.

Conditions affecting the sensory nerves (sensory peripheral neuropathies), such as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).

Friedreich’s ataxia

Ménière’s disease

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24
Q

Which three pathological features cause clinical manifestations in Multiple Sclerosis?

A

Inflammation, Demyelination and Axonal Loss

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25
Q

What is the gait of somebody with lower limb weakness?

A

High stepping and waddling gait (slapping sound)

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26
Q

Which CNS infection is most indicated when you see a non blanching rash - especially if return travellers?

A

Haemophilus Influenza

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27
Q

How does Brainstem Demyelination present in Multiple Sclerosis?

A

Brainstem Demyelination produces diplopia (double vision), vertigo, dysphagia (difficulty swallowing), dysarthria (motor speech disorder), facial weakness/numbness & nystagmus. A typical picture is sudden diplopia and vertigo with nystagmus, but without tinnitus or deafness. Bilateral internuclear ophthalmoplegia is pathognomonic of MS. (Eye shows impairment in adduction & double vision)

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28
Q

What is the Q Risk?

A

Probability of cardiovascular event in next ten years

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29
Q

What would show on a CT as a crescent shaped mass?

A

A subdural haemorrhage

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30
Q

What supportive care should be offered to patients who have had a stroke?

A

Swallowing and Feeding. Dysphasia is common and may cause aspiration pneumonia and nutritional deficit. Speech & Language therapists make assesment within 42-72 hours.

Admission to stroke unit improves outcome.

Unconscious patient - maintenance of hydration, frequent turning.

Prevention of DVT by anti-embolism (T.E.D.) stockings. Heparin is not given.

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31
Q

What are the symptoms of Cerebellar Syndrome?

A

Vertigo, Headache, Ataxia, Vomiting

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32
Q

A patient presents with leg weakness, sensory disturbance in the legs, gait apraxia, incontinence, drowsiness and akinetic mutism (decrease in spontaneous speech) - you suspect an ischaemic stroke. Which artery is the most likely to be blocked?

A

Anterior Cerebral Artery

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33
Q

What are some of the signs of an upper motor neurone lesion?

A

Muscle tone increased (spasticity),
Tendon reflexes are brisk, Plantar responses (babinski sign), Characteristic pattern of limb muscle weakness (pyramidal pattern) -
Upper limbs - extensor muscles weaker than flexors,
Lower limbs flexors weaker than extensors, finer more skilful movements most severely impaired, emotional liability may be present (may laugh or cry easier than normal.

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34
Q

What are some of the causes of subacute headaches (days to weeks)?

A
Intracranial mass lesion
Encephalitis
Meningitis
Giant Cell Arteritis
Sinusitis
Acute Glaucoma
Malignant Hypertension
35
Q

What are some of the symptoms of Friedreich’s Ataxia?

A
Muscle weakness in the arms and legs
Loss of coordination
Vision impairment
Hearing impairment
Slurred speech
Curvature of the spine (scoliosis)
High plantar arches (pes cavus deformity of the foot)

Diabetes (about 20% of people with Friedreich’s ataxia develop carbohydrate intolerance and 10% develop diabetes mellitus)

Heart disorders (e.g., atrial fibrillation, and resultant tachycardia (fast heart rate) and hypertrophic cardiomyopathy)

36
Q

What are some of the causes of recurrent/chronic headaches?

A
Migraine
Tension Headache
Sinusitis
Cluster Headaches
Paroxysmal hemicrania
Medication overuse
Intracranial Mass Lesion
37
Q

What is the first line treatment for epilepsy?

A

Carbamazepine or lamotrigine

38
Q

Which fibres transmit pain?

A

A delta and C fibres

39
Q

What marker can be seen to differentiate an astrocytoma on histology?

A

p67 is a marker of astrocytoma

40
Q

What is coning?

A

When brain matter is pushed through holes such as the foramen magnum due to high intracranial pressure.

41
Q

What are Brudzinski’s Sign and Kernig’s Sign? What are they indicative of?

A

Brudzinskis: When the patients neck is flexed by the physician the patient will flex their hips and knees

Kernig’s Sign: The physician is unable to extend the patient’s leg at the knee greater than 145 degrees when the thigh is flexed due to stiffness of the hamstrings

Indicative of Meningeal irritation (e.g. meningitis or subarachnoid haemorrhage)

42
Q

A patient presents with contralateral homonymous hemianopia, cortical blindness with bilateral involvement of the occipital lobe branches, visual agnosia (can see, but can’t interpret visual information), prosopagnosia, dyslexia, anomic aphasia and unilateral headaches. Which artery is most likely blocked?

A

Posterior Cerebral Artery

43
Q

What are the symptoms of cerebellar disease?

A

Slurring of Speech (staccato),
Swallowing DIfficulties,
Oscillopsia (illusion of things moving),
Clumsiness,
Action tremor,
Loss of precision of fine movement or motor skills
Unsteadiness when walking - worse in the dark
Stumbles and falls.

44
Q

What are some of the common causes of motor neurone lesions?

A

Vascular Disease (eg CVA, stroke), inflammatory lesions (MS), Compression of brain or spine (eg by a tumour or degenerative spinal disease spondylitis), infiltration of portico spinal pathway, neurodegrenertive disease of UMN and or LMN - motor neurone disease, hereditary.

45
Q

A patient presents with contralateral arm and leg weakness, contralateral sensory loss, hemianopia, aphasia, dysphasia and a facial droop - you suspect an ischaemic stroke. Which artery is the most likely to be blocked?

A

Middle Cerebral Artery

46
Q

What is the gait of somebody with Parkinson’s disease?

A

Shuffling Gait - posture is stooped and arm swing is reduced. Gait becomes festinant with short rapid steps and slows to a shuffle in advanced forms. Difficulty in turning quickly. Freezing episodes may develop.

47
Q

What are the clinical signs of cerebellar damage?

A
VANISHED
Vertigo
Ataxia
Nystagmus
Intentional Tremor
Slurred Speech
Hypotonia
Exaggerated Broad Based Gait
Disdiadokinesia
48
Q

What are some of the signs of a lower motor neurone lesion?

A

Muscle tone reduced, Muscle bulk goes down, Reflexes depressed or absent, Fasciculation - most patients actually die from respiratory diseases.

49
Q

How is Multiple Sclerosis managed? (8)

A

Short courses of steroids, e.g IV methylatednisolone 1000mg/day for 3 days, are used in relapses and may reduce severity. However not influencing on long term outlook.

Subcutaneous administration of ß-interferon reduces the relapse rate by one-third in relapsing/remitting disease and may delay the time to severe debility. Treatment is prolonged, expensive and associated with side effects such as flu-like symptoms. Prevention of immune activation.

Glatiramer acetate is antigenically similar to myelin basic protein and competes with various myelin antigens for their presentation to T cells. It has similar efficacy to interferons and is given by subcutaneous injection.
Prevention of immune activation.

Monocloncal Antibodies can be used - BD12, CD20, CD52

Physiotherapy & Occupational Therapy maintain the mobility of joints and muscle relaxants (e.g. baclofen, dantrolene and bendiazepines) reduce the discomfort and pain of spasticity. Multidisciplinary team liaison is essential.

Urinary cathetersation for those with bladder involvement.

Sexual Dysfunction issues need to be addressed.

Psychological Symptoms should also be appropriately treated

50
Q

Which sensory fibres tranmit cold sensation?

A

A delta

51
Q

Which motor neurone disease gets progressively worse throughout the day?

A

Myasthenia Gravis

52
Q

What is Friedreich’s ataxia?

A

Friedreich’s ataxia is an autosomal recessive inherited disease that causes progressive damage to the nervous system (affects mainly spinal cord and causes demyelination).
It manifests in initial symptoms of poor coordination such as gait disturbance; it can also lead to scoliosis, heart disease and diabetes, but does not affect cognitive function. The disease is progressive, and ultimately a wheelchair is required for mobility.

53
Q

Which medication can counteract warfarin?

A

Beriplex - pharmacological version of Vitamin K

54
Q

How Do Spinal Cord Lesions present in MS?

A

Sensory symptoms, including numbness and pins and needles are common. This reflects spinothalamic and posterior column lesions. Spastic parasthesis is the result of plaques of demyelination in the cervical or thoracic cord. White matter affected

55
Q

When must dexamethasone not be given?

A

Later than 14:00 - will stop patient from sleeping - the most powerful synthetic steroid

56
Q

How are brain tumours graded?

A

Grade I is a paediatric tumour - benign and very curable

Grade II - is a premalignant tumour - “benign”

Grade III - is called anapaestic astrocytoma - cancer. - malignant at diagnosis

Grade IV - Glioblastoma multiforme (GBM) the most common phenotype

57
Q

Which spinal pathway is associated with upper motor neurone?

A

Corticospinal Tract

58
Q

What is the main risk factor for epilepsy?

A

Childhood febrile convulsions

59
Q

Which antibiotic is most commonly used to treat neurological infections?

A

Cefotaxime

60
Q

What is Guillain Barré syndrome?

A

Guillain–Barré syndrome (GBS) is a rapid-onset muscle weakness caused by the immune system damaging the peripheral nervous system. The initial symptoms are typically changes in sensation or pain along with muscle weakness, beginning in the feet and hands.
This often spreads to the arms and upper body, with both sides being involved. The symptoms develop over hours to a few weeks.

During the acute phase, the disorder can be life-threatening, with about 15% developing weakness of the breathing muscles requiring mechanical ventilation.

61
Q

Which non-pharmacological treatment has been successful in treating Parkinsons?

A

Deep Brain Stimulation

Physiotherapy

62
Q

How will a patient with spasticity walk?

A

More pronounced in extensor muscles. Stiff, slow walking - pace shortens, a narrow base is maintained

63
Q

What is the main pathological cause of temporal lobe epilepsy?

A

Hippocampal Sclerosis

64
Q

What are some of the physical signs of Friedreich’s Ataxia?

A

Cerebellar: nystagmus, fast saccadic eye movements, truncal ataxia, dysarthria, dysmetria.

Lower motor neuron lesion: absent deep tendon reflexes.

Pyramidal: extensor plantar responses, and distal weakness are commonly found.

Dorsal column: Loss of vibratory and proprioceptive sensation occurs.

Cardiac involvement occurs in 91% of patients, including cardiomegaly, symmetrical hypertrophy, heart murmurs, and conduction defects.

Median age of death is 35 years, while females have better prognosis with a 20-year survival of 100% as compared to 63% in men

65
Q

What are some of the causes of acute sever headaches?

A
Intracranial haemorrhage
Cerebral venous thrombosis
Dissection of carotidvertebrobasilar arteries
Meningitis
Head Injury
Migraine
Drugs (GTN Spray)
Alcohol
Infections such as malaria
66
Q

Which group of tumours is the most common of all primary brain tumours?

A

Neuroepithelial Tumours - astrocytic, oligodendroglial, ependymal, neuronal, pineal, embryonal (60%)

67
Q

Which tumours most commonly have metastases to the brain?

A

Lung (Breast & Melanoma also have a high amount of mets in brain)

68
Q

Which area of the brain is affected in Parkinsons and what is found there in the disease?

A

Substantia Nigra - you will find Lewy Bodies which cause reduced dopamine supply

69
Q

How is a stroke immediately managed?

A

Ischaemic: 1st line: Thrombolysis
2nd line: Aspirin 300mg for 2 weeks then Clopidogrel 75mg OD

Haemorrhagic: Control BP: B-blocker
Beriplex if warfarin-related bleed
Clot evacuation

70
Q

How do you assess a patients risk of stroke in the next seven days?

A

ABCD2 Score: If 4 or more

A - Age: Above 60 years or more (1 point)

B - BP 140 or higher

C - Clinical Features - unilateral weakness or speech disturbance

D - Duration - 60 minutes or longer, 2 points, 10 - 59, 1 point

D - Presence of diabetes - 1 point

71
Q

What treatment should be given to someone having a prolonged seizure (more than 3 minutes)?

A

Rectal or IV diazepam or lorazepam.

72
Q

Which headache pain is the ‘worst ever’?

A

Subarachnoid Haemorrhage

73
Q

How is Charcot Marie Tooth Disease characterised?

A

Characterized by progressive loss of muscle tissue and touch sensation across various parts of the body. Peripheral Nerves

74
Q

What is gait apraxia?

A

With frontal lobe disease, walking skills become disorganised despite normal motor and sensory function. The gait is shuffling with small steps, gait ignition failure and hesitancy. Arm swing and posture are normal. Urinary incontinence and dementia are often present.

75
Q

What are the three cardinal presenting signs of brain cancer?

A

Three Cardinal Presenting Symptoms:
Symptoms of raised ICP (Intercranial Pressure) - Headache, reduced conscious level, nausea & vomiting - combination of the two

Progressive Neurological Deficit

Epilepsy

76
Q

What are the four pharmacological treatments for Parkinsons?

A

Levodopa (combined with a peripheral dopa-decarboxylase inhibitor)

Dopamine Agonists

Monoamine Oxidase B Ibhibitors

Selective Serotonin Reuptake Inhibitors

77
Q

An elderly patient complaining of generalised aches and pains as well as a headache suggests which condition ? What is the treatment?

A

Giant Cell Arteritis - urgent treatment with steroids to prevent blindness.

78
Q

Which sensory fibres transmit light touch, pressure and vibration?

A

A Beta

79
Q

How does a generalised tonic-clonic seizure present?

A

Sudden onset of a rigid tonic phase followed by a convulsion (clonic phase) in which the muscles jerk rhythmically and the eyes remain open. Episode typically lasts for seconds to minutes, may be associated with tongue biting and incontinence of urine - followed by a period of flaccid unresponsiveness, followed by confusion or drowsiness.

80
Q

What is the difference between Delirium and Dementia?

A

Delirium acute, dementia chronic.

81
Q

Which genetic combination can be seen in 70% of Oligodendrogliomas? What does this indicate?

A

1p & long arm of 19q are deleted. This indicates that the tumour will respond better to chemotherapy - and prognosis is better.

82
Q

Which of Brodmann’s Areas is associated with motor function?

A

Area 4

83
Q

What genetic mutation indicates better prognosis in astrocytomas?

A

IHD1 mutation - related to alphaketoglutarate.

84
Q

Which tumour is the most common primary brain tumour?

A

Diffuse Astrocytoma