Neurology Flashcards

1
Q

Creutzfeldt-Jakob disease

A

Deposition of abnormal prion proteins causing progressive neurodegeneration
- Majority sporadic

Features:
- Early - anxiety, personality change, neurosis, forgetfulness, hallucinations
- Late - myoclonus, ataxia, dementia, akinetic mutism, seizures

Investigations:
- EEG
- Triphasic sharp waves
- Myoclonic spikes
- Generalised suppression
- RT-QuIC on CSF
- MRI brain
- Autopsy

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2
Q

Stroke and driving advice

A

No driving for 1 month after stroke with mild deficit or TIA

If severe persistent neurology, must discuss with DVLA

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3
Q

Lateral medullary / Wallenberg’s syndrome

A

Classically due to occlusion of the posterior inferior cerebellar artery

Features:
- Cerebellar
- Ipsilateral limb ataxia - cerebellar peduncle
- Vertigo
- Nystagmus to side of lesion
- Brainstem
- Sudden dizziness + vomiting = [VIII]
- Dysphagia + dysarthria
- Ipsilateral Horner’s syndrome
- Ipsilateral facial pain/temp loss = [V]
- Ipsilateral IX + X palsies
- Contralateral limb/truncal pain/temp loss
(spinothalamic)

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4
Q

Meralgia paraesthetica

A

Entrapment neuropathy or neuroma of the lateral cutaneous nerve
- L2/L3 fibres via the lumbar plexus
- Runs under or through the inguinal ligament
- Main risk factor is obesity or weight gain

Features:
- Numbness, parasthesia, pain in the anterolateral thigh

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5
Q

Lumbar spinal stenosis

A

Narrowing of the lumen of the lumbar canal, usually due to progressive hypertrophy of the facet joints + disc degeneration

Features:
- Cramping or burning pain in leg with evidence of neurogenic claudication
- Alleviated by leg flexion, sitting, forward
flexion of lumbar spine
- ‘shopping cart’ sign
- Lower extremity muscle weakness
- Diminished reflexes
- Parasthesias
- Impaired balance

Management:
- Medications - unclear benefit, can trial NSAIDs and SSRIs
- Physiotherapy
- Spinal decompression surgery

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6
Q

Tuberculous meningitis

A

Features:
- Subacute timescale
- Asymmetrical neuropathies - esp. [III] and [V]
- Fever
- Headache
- Confusion
- Meningism
- Weight loss
- Raised ICP

Risk factors:
- HIV
- Malignancy
- Malnutrition

Investigations:
- LP - low glucose, high protein, lymphocytosis, mildly raised opening pressure
- Send CSF for NAAT, AFB, and culture
- Screen for comorbid HIV
- Imaging:
- MRI head
- CXR chest

Management:
- 2/12 RIPE then a further 7-10/12 RI
- 8/52 dexamethasone with taper

Complications
- Cranial nerve palsy
- Cerebral oedema
- Venous sinus thrombosis

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7
Q

Syringomyelia

A

Aetiology:
- Congenital - typically Chiari malformation
- Post-traumatic

Features:
- Shawl-like loss of pain and temperature sensation
- Can also affect [V]
- If post-traumatic, symptoms spread upwards
from site of trauma

Management:
- Surgical decompression

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8
Q

Mononeuritis multiplex

A

A sensory and/or motor peripheral neuropathy affecting at least two different nerves
- Painful
- Asymmetrical

Aetiology:
- Diabetes mellitus
- Autoimmune e.g. SLE, vasculitis
- Infection e.g. Lyme disease, leprosy
- B12 deficiency
- Sarcoidosis

Complications include recurrence, deformity, and muscle atrophy

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9
Q

Median nerve neuropathy

A

Aetiology:
- Carpal tunnel syndrome
- Trauma

Risk factors:
- Pregnancy
- Obesity
- Rheumatoid arthritis
- Hypothyroidism
- Occupational

Features:
- Tinel’s and Phalen’s positive
- Weakness of 1st + 2nd lumbricals, OPB, APB, FPB
- Sensory loss thumb, forefinger, middle finger, 1/2 ring finger

Management:
- Analgesia
- Splinting
- Steroid injection
- Surgical release

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10
Q

Ulnar radiopathy at the elbow

A

aka cubital tunnel syndrome

Most commonly due to trauma

Features:
- Weakness of FCU, dorsal and palmar interossei, hypothenar muscles
- Sensory loss + paraesthesias along 1/2 of 4th + little finger
- Pain at elbow
- Froment’s +ve

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11
Q

Radial nerve palsy

A

Aetiology:
- Trauma
- Compression or damage of the radial nerve in
the spinal groove of the humerus
- Inflammatory
- Infection

Features:
- Wrist drop
- Sensory loss over dorsum of hand and 1st web space

Management:
- If compressional, usually spontaneously recovers within 6 weeks
- Cock-up wrist and finger splints
- Physiotherapy to prevent flexion contracture

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12
Q

Femoral neuropathy

A

Aetiology:
- Retroperitoneal haematoma
- Hip dislocation
- Lithotomy positioning

Features:
- Impaired hip flexion and knee extension
- Sensory loss anteromedial leg
- Reduced patellar reflex

Management:
- Usually self-limiting

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13
Q

Sciatic neuropathy

A

Usually due to the peroneal division of the sciatic nerve

Aetiology:
- Trauma during hip arthroplasty
- Prolonged lithotomy positioning
- Vasculitis
- Tumour
- Idiopathic

Features:
- Weakness of ankles and toes
- Sensory loss in foot and distal lateral leg
- Reduced ankle and hamstring reflexes

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14
Q

Peroneal neuropathy

A

Most common lower limb neuropathy

Due to compression at the lateral border of the knee

Features:
- Foot drop
- Weak foot eversion
- Flail foot
- Sensory loss dorsum of foot + lateral border of shin

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15
Q

Neurological disease in HIV

A

Split into focal and generalised disorders:
- Focal
- Toxoplasmosis
- TB meningitis or abscess
- Generalised
- PML - JC virus
- CMV encephalitis
- Cryptococcal meningitis
- Atypical neurosyphilis - myelopathy, retinitis,
meningitis.

Meningitides:
- Non-specific fever, headache, meningism
- Cryptococcal - subacute (1-2 weeks) with
disorientation and confusion
- TB - subacute (2-4 weeks) with consitutional sx

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16
Q

Lambert-Eaton myasthenic syndrome

A

Aetiology:
- Paraneoplastic
- SCLC, ovarian Ca, breast Ca
- Non-neoplastic
- T1DM, thyroid disorders

Pathophysiology:
- Formation of autoantibodies to pre-synaptic P/Q-type voltage-gated calcium channels
- Impairs neurotransmitter release
- Rarely has eye/bulbar involvement

Features:
- Proximal weakness of lower limbs
- Dry mouth
- Hypo-/a-reflexia
- Impotence
- Dysphagia
- Dizziness on standing
- Muscle fatiguability but with temporary increase in power after exercise

Investigations:
- Imaging - to find underlying malignancy
- EMG
- Muscle biopsy

Management:

17
Q

Myasthenia gravis

A

Aetiology:
- Anti-AChR antibodies (90%) or anti-MuSK (10%) antibodies
- Associated with HLA-B8 and -DR3
- Ocular MG associated with HLA-DR1

Features:
- Painless fatiguable skeletal muscle weakness
- Ophthalmoplegia
- Dysarthria
- Dysphonia
- Dysphagia
- Loss of facial expression - myasthenic snarl
- Myasthenic crisis
- Life-threatening respiratory weakness
- Abnormalities of the thymus

Investigations:
- Serology - anti-AChR and anti-MuSK
- TFTs
- Single-fibre EMG
- Ice-pack test
- CT/MRI chest

Management:
- Crisis:
- IVIg, plasmapheresis, I+V
- Other:
- Initially pyridostigmine + steroids, then can
switch to steroid-sparing agents
- Thymectomy can be beneficial

18
Q

Weber syndrome

A

Classically due to occlusion of the paramedian branches of the posterior cerebellar artery
- Causes midbrain symptoms

Features:
- Ipsilateral [III] palsy
- Contralateral hemiparesis and parkinsonism

19
Q

Origins of cranial nerves

A

Cerebrum - [I] + [II]

Midbrain - [IV]

Midbrain-pontine junction - [III]

Pons - [V]

Pontine-medulla junction - [VI] + [VII] + [VIII]

Medulla - [IX] + [X] + [XI] + [XII]

20
Q

Miller-Fischer syndrome

A

A variant of GBS
- Associated with anti-ganglioside GQ1B
- Affects brainstem, cranial nerves, peripheral nerves
- CSF - cytoalbuminologic dissociation

Features:
- Ophthalmoplegia
- Ataxia
- Areflexia

Management:
- Respiratory monitoring
- IVIg
- Plasmapheresis

21
Q

Orbital apex syndrome

A

A syndrome involving [II] + [III] + [IV] + [VI] +/- [V2]

Can be traumatic or secondary to a tumour

Features:
- Optic neuropathy
- Unilateral Horner’s syndrome
- Chemosis
- Ophthalmoplegia
- Possible loss of V2 sensation and corneal reflex