Almostadoctor topics Flashcards

(37 cards)

1
Q

Define a cerebral aneurysm

A

A localised dilation of an artery within the brain

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2
Q

Give some risk factors for cerebral aneurysm development

A

Arteriosclerosis
HTN
Hereditary CT disorders
Septic emboli

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3
Q

Why are cerebral aneurysms called berry aneurysms?

A

Made up of many small sacs which bulge out from the vessel wall

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4
Q

What are the different surgical treatment options for cerebral aneurysms?

A

Clipping
Platinum coiling
Stenting

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5
Q

At what diameter are cerebral aneurysms operated on?

A

7mm or more

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6
Q

Define an ateriovenous malformation

A

An abnormal connection between arteries and veins which bypasses the capillary circulation

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7
Q

Where do AVMs usually occur?

A

Junction of cerebral arteries.

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8
Q

What investigation determines if the cerebral ANM is operable or not?

A

Arteriography

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9
Q

What are the treatment option for AVMs?

A

Watch and wait
Treat symptom only (epilepsy)
Radiotherapy (<3cm in size)
Surgery (larger, more superficial lesions) such as embolisation

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10
Q

What symptoms can AVMs cause?

A

88% are asymptomatic
Headache
Epilepsy
Specific symptoms can give an idea of the location

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11
Q

What can cause AVMs?

A

Hereditary Haemorrhagic telangiectasia (autosomal dominant)

Von Hippel-Lindau Disease

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12
Q

Describe Bulbar palsy

A

Lesion in the motor nuclei of the medulla which causes LMN signs in the facial, glossopharyngeal, vagus and hypoglossal nerve regions

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13
Q

What are the symptoms of bulbar palsy?

A
Tongue palsy
Facial muscle palsy
Swallowing palsy 
Flacid and fasciculating tongue 
Normal jaw jerk (CN5 intact)
May have quiet, hoarse or nasal speech
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14
Q

What conditions can cause bulbar palsy?

A
MND
Guillan-Barre
Polio
Syringobulbia 
Brainstem tumours
Myasthenia gravis
Myotonic dystrophy
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15
Q

Describe pseudobulbar palsy

A

Bilateral lesions of UMNs of muscles of regions for facial, vagus, glossopharyngeal and hypoglossal nerves. The lesion commonly occurs inthe corticobulbar tracts.

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16
Q

What are some symptoms of pseudobulbar palsy?

A
Spastic tongue (cannot protrude)
"Donald Duck" speech 
Increased jaw jerk 
Reduced rate of blinking
Emotional lability
17
Q

What are some causes of pseudobulbar palsy?

A
Bilateral cerebral vascular accident affecting the internal capsule
Multiple sclerosis
Motor neuron disease
Stroke 
Vascular dementia
18
Q

Define Charcot Marie Tooth diesease

A

An inherited peripheral neuropathy, commonly autosomal dominant

19
Q

What is the pathology of Charcot Marie Tooth disease?

A

Type 1 - gene mutations for myelin sheath growth

Type 2 - Mutations for mitochondria found in the nerves lead to improper nerve conduction

20
Q

What are the symptoms of Charcot Marie Tooth disease?

A
  • Progressive distal muscle weakness and wasting which causes gait changes
  • Loss of reflexes and sensation
  • Normal tone, slight reduction in power
  • Champagne bottle legs appearance (peroneal muscle wasting)
  • Pes cavus
  • Hammer toe
21
Q

What is the management of Charcot Marie Tooth disease?

A
Incurable
Encourage activity 
Hydrotherapy 
Keep weigth low 
Genetic testing 
Surgery can reduce deformities e.g. clawed toes, pes cavus
22
Q

Define encephalitis

A

Inflammation of the brain parenchyma usually due to a viral infection.

23
Q

What are the most commonly implicated organisms for encephalitis?

A
Herpes simplex virus 
Rabies 
Measles 
Epstein Barr virus 
Poliovirus 
Coxsackievirus
24
Q

What are the clinical features of encephalitis?

A
Headache
Drowsiness
Pyrexia
Malaise 
Meningeal signs
25
Give some parenchymal signs
``` Seizures Confusion Dysphasia Cranial nerve palsies Ataxia Hemiparesis May have sings of underlying cause e.g. cold sore for herpes simplex, parotid gland swelling for mumps ```
26
What are the investigations you should do if you suspect encephalitis?
Viral serology PCR of blood Lumbar puncture (only if intracranial mass has been excluded on scan) CT scan MRI scan - shows more subtle changes EEG Test for cause e.g. HIV serology, Mantoux test
27
What is the management of someone with encephalitis?
HDU/ICU care IV aciclovir for 2-3 weeks Anticonvulsants if seizures are present Dexamethasone for raised ICP
28
Describe Friedreichs ataxia
Autosomal recessive disorder due to repeating nucleotide sequence (GAA) in the frataxin gene which codes for the mitochondrial protein frataxin. This cause mitochondrial iron overload, impairing mitochondrial function.
29
What are the signs and symptoms of friedreichs ataxia?
- Wide based ataxic gait - Upper limb weakness - Nystagmus - Lower limb paresis - Reduced/absent reflexes - Loss of vibration and proprioception
30
What is the treatment for Friedreich's ataxia?
No cure Life expectancy is 50 years Treat associated conditions Surgery to improve symptoms (pes cavus)
31
What conditions is Friedreichs ataxia associated with?
Diabetes Heart disorders e..g AF and hypertrophic cardiomyopathy Scoliosis Pes cavus
32
What is Guillain Barre syndrome?
An acute inflammatory demyelinating polyneuropathy which tends to occur several weeks after a viral infection (GI or URTI).
33
Describe the clinical course of Guillain Barre
Symmetrical muscle weakness which begins in the legs and moves to the arms. Progresses over 4 weeks then resolves. Tend to affect proximal muscles more. No sensory involvement Autonomic signs include tachycardia, dysrhythmias and sweating. Can involve respiratory muscles and cranial nerves/
34
Describe the pathology of Guillain Barre syndrome
Viral infection leads to the production of auto-antibodies which attack peripheral nerve, damaging the myelin sheaths. This reduces or block nerve transmission.
35
What investigations do you do for Guillain Barre syndrome?
Lumbar puncture will show increase CSF protein with a normal white cell count Nerve conduction studies will show a decrease speed of conduction
36
What is the prognosis for Guillain Barre?
85% - complete/almost complete recovery 10% - unable to walk at 1 year 10% mortality
37
What is the treatment for Guillain Barre?
Ventilation IV immunogloblin Plasmapheresis