Clinical Clues & Presenting Problems Flashcards

1
Q

What are the features of a frontal lobe lesion?

A
Personality change 
Primitive reflexes, e.g. grasp, pout 
Anosmia 
Optic nerve compression (atrophy) 
Gait apraxia 
Leg weakness (parasagital)
Loss of micturition control 
Dysphasia (expressive - damage to Broca's area in the inferior frontal lobe)
Seizures
Proverb interpretation lost
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the features of a parietal lobe lesion?

A

Dysphasia (dominant)
Acalculia, agraphia, left-right disorientation, finger agnosia
Sensory and visual inattention, construction and dressing apraxia, spatial neglect and inattention
Lower quadrantic hemianopia (PITS)
Astereognosis (inability to identify an object by touch)
Seizures

  • = Gertsmann’s syndrome: dominant hemisphere parietal lobe ONLY
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are non-dominant parietal lobe features?

A

Sensory and visual inattention
Construction and dressing apraxia
Spatial neglect and inattention

(Most patients are left-hemisphere dominant)

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

What are the features of a temporal lobe lesion?

A

Memory loss
Upper quadrantic hemianopia
Epilepsy

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

What are the features of an occipital lobe lesion?

A

Homonymous hemianopia (with macular sparing)
Alexia
Epilepsy (flashing light aura)
Cortical blindness (Anton’s syndrome, bilateral occipital lobe lesions)

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

What is dysphasia?

A

This is defined as a dominant cortical disorder of the use of written and verbal symbols for communication

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

What are the features of receptive dysphasia?

A

Caused by damage to Wernicke’s area (dominant superior temporal lobe).
Comprehension is impaired.
Naming objects is poor.
Repetition poor.
Fluency and prosody preserved but uses jargon, paraphasias and neologisms.

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

What are the features of expressive dysphasia?

A

Caused by damage to Broca’s area (third frontal convolution or inferior frontal lobe).
Comprehension intact.
Naming objects is poor.
Repetition poor, may be possible with great effort.
Fluency decreased to anarthria.

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

What are the features of conductive dysphasia?

A
Caused by damage to the arcuate fasciculus and/or conducting fibres. 
Comprehension intact. 
Naming objects poor. 
Repetition poo. 
Fluency preserved but paraphasic.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is nominal dysphasia?

A

Caused by damage to the angular gyrus (temporal lobe).
Comprehension intact.
Naming objects poor.
Repetition normal.
Fluency normal except for naming objects.

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

What is dysarthria?

A

Disordered articulation with normal speech content.
Test by asking the patient to say “British constitution”

Causes:

  • cerebellar disease - arrhythmic or explosive speech or speech broken into syllables
  • bilateral UMN disease - trying to squeeze words out; described as a harsh or strained quality
  • bilateral LMN disease - nasal speech; a “hot potato” in the mouth
  • bilateral facial nerve palsies - slurred speech secondary to labial weakness
  • extrapyramidal - monotonous, low volume, mumbled
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Name some causes of anosmia

A

Bilateral:
Upper respiratory tract infection
Meningioma of the olfactory groove (late)
Ethmoid tumours; head injury (including cribriform plate fracture)
Meningitis
Hydrocephalus
Kallman’s syndrome (hypogonadotrophic hypogonadism)

Unilateral:
Head trauma
Meningioma of the olfactory groove (early)

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

Give some causes for rapid onset bilateral blindness

A

Bilateral occipital lobe infarction
Ischaemia or trauma
Severe bilateral papilloedema
Rapidly progressive optic chiasmal compression
Bilateral optic nerve damage (e.g. methyl alcohol poisoning)

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

Give some causes for rapid onset unilateral blindness

A
Retinal artery embolism
Retinal vein thrombus 
Vitreous haemorrhage 
Temporal arteritis 
Retinal detachment 
Optic neuritis 
Ischaemic optic neuropathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Give some causes for gradual onset blindness

A

Cataracts
Glaucoma
Diabetic retinopathy
Bilateral optic nerve or chiasmal compression
Bilateral optic nerve inflammation or ischaemia
Bilateral retinal disease

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

What are the features of papilloedema?

A
Optic disc is swollen without venous pulsation.
Normal visual acuity (early)
Large blind spot 
Normal pupillary light reflex 
Peripheral constriction of fields
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What are the features of retrobulbar neuritis?

A
This is different from papilloedema 
Optic disc appearance acutely is normal
Poor acuity
Large central scotoma 
Afferent pupillary defect 
Pain on eye movement 
Onset usually sudden and unilateral
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Give some causes of papilloedema

A

Space occupying lesions causing raised intracranial pressure
Any cause of cerebral oedema (e.g. head trauma)
Acute hydrocephalus (associated with large ventricles)
Benign intracranial hypertension
Hypertension (grade IV)
Central retinal vein thrombosis
Retro-orbital mass

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

What is the Foster-Kennedy syndrome?

A

This is an unsual cause of papilloedema.
A unilateral anterior fossa tumour causes raised intracranial pressure and optic nerve compression simultaneously resulting in papilloedema in the contralateral eye and optic atrophy in the ipsilateral eye.

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

What is associated with idiopathic intracranial hypertension?

A
Idiopathic 
Drugs (e.g. contraceptive pill, nitrofurantoin, tetracycline, vitamin A/ retinoids, steroids 
Addisons disease 
Venous sinus thrombosis 
Trauma 
Obesity
21
Q

What causes tunnel vision?

A

Concentric diminution - e.g. glaucoma, papilloedema, syphilis

22
Q

What causes a central scotoma?

A

Optic nerve head to chiasmal lesion - e.g. demyelination, toxic, vascular, nutritional

23
Q

What causes a bitemporal hemianopia?

A

Lesions at the optic chiasma - e.g. pituitary tumour or sella meningioma
Lesions from below (i.e. pituitary tumours) causes an upper quadrant defect
Lesions from above (i.e. suprasellar) cause a lower quadrant defect

24
Q

What causes a homonymous hemianopia? What is the difference between a congruous and an incongruous lesion?

A

Lesions of the optic tract to occipital cortex at any point, e.g. vascular, tumour

Incongruous lesions = lesions of the optic tract, these are incomplete or asymmetric

Congruous lesions = lesions of the optic radiation or cortex

25
What is the site of a lesion for a homonymous quadrantinopia?
"PITS" Parietal inferior, temporal superior When plotting quadrantanopia, the segment points towards the site and location of the lesion
26
Name some causes of a constricted pupil
Pupillary constriction is mediated by the parasympathetic nervous system and is called miosis ``` Horners syndrome Argyll Robertson pupil (prostitutes pupil; accommodates but won't react) Pontine lesion (bilateral) Opioids Pilocarpine drops Elderly ```
27
Name some causes of a dilated pupil
Pupillary dilatation is mediated by the sympathetic nervous system ``` Mydriatic drops or atropine poisoning Third nerve lesion Adie's pupil (decreased reactivity) Post trauma, deep coma, cerebral death Amphetamine or glutethimide overdose Cocaine, anxiety Iritis Anticholinergic drugs ```
28
What is Holmes-Adie syndrome?
This refers to a dilated pupil with virtually no reaction to light, a slow reaction to accommodation and absent ankle reflexes. Other tendon reflexes may also be absent
29
What is Horner's syndrome?
This refers to partial ptosis; constricted pupil, apparent enophthalmos, decreased sweating over the ipsilateral face (but only when the lesion is below the carotid bifurcation); elevation of the lower lid; conjunctival injection
30
What causes a Horner's syndrome?
The clue is the location of the anhidrosis If sweating is absent from the face, torso and arm then this is a CENTRAL lesion - stroke, syringomyelia, multiple sclerosis, tumour or encephalitis If sweating is absent from the face only then this is a PRE-GANGLIONIC lesion - Pancoast's tumour, thyroidectomy, trauma, cervical rib If there is no anhidrosis then this is a POST-GANLIONIC lesion - carotid artery dissection, carotid aneurysm, cavernous sinus thrombosis, cluster headache (the C's)
31
What is the lateral medullary syndrome?
This is also known as Wallenberg's syndrome. It is due to vertebral or posterior inferior cerebellar artery (PICA) thrombosis. The patient presents with vertigo, Horner's syndrome, ipsilateral V (pain and temperature loss), IX and X nerve palsies, ipsilateral cerebellar signs and contralateral loss of pain and temperature over the trunk and limbs.
32
What are the clinical features of a third nerve palsy?
``` Complete ptosis (if lesion is complete) Eye "down and out" Dilated pupil unreactive to light (consensual response intact in the unaffected pupil) or accommodation (sympathetic response is mediated by the second nerve) ```
33
What are the causes of a third nerve palsy?
Central lesion: brainstem infarct, tumour Peripheral lesion: aneurysm (usually on posterior communicating artery), tumour causing raised ICP (dilated pupil occurs early), infarction (typically in diabetics - pupil is spared because the inner fibres control pupillary dilatation)
34
What are the features of a fourth nerve palsy?
This produces diplopia maximum when the eyes looks "down and in", tilting the head to the side of the lesion results in a failure of the affected eye to intort. Supplies the superior oblique (LR6 SO4) Most common cause is a head injury, but can be idiopathic. May be associated with a IIIrd nerve palsy, but rarely may occur as an isolated defect due to a lesion of the contralateral cerebral peduncle (the IV nerve crosses after exiting the brainstem)
35
What causes a sixth nerve palsy?
This produces failure of lateral eye movement and diplopia. Bilateral - Wernicke's encephalopathy, mononeuritis multiplex, trauma with raised ICP Unilateral - central (vascular, tumour), peripheral disease (e.g. trauma), idiopathic NB - myasthenia and thyroid eye disease can cause "pseudo" 6th nerve palsies
36
What is jerk nystagmus?
This is an alternation between slow phase drift followed by rapid corrective saccade in the opposite direction It can be horizontal, conjugate (both eyes move together), disconjugate or vertical
37
What causes conjugate jerk nystagmus?
``` Brainstem lesions especially in the medulla Vestibular lesions Cerebellar lesion Phenytoin and other drugs Alcohol intoxication ```
38
What causes dysconjugate jerk nystagmus?
``` Dysconjugate means that the eyes move in opposite directions or that only one eye is affected. Internuclear ophthalmoplegia (INO) due to lesion of the median longitudinal fasciculus is the classic cause of dysconjugate jerk horizontal nystagmus. ``` Here is nystagmus of the abducting eye with failure of adduction of the eye on the affected side. If in a young patient with bilateral involvement, multiple sclerosis is almost always the cause; in the elderly consider brainstem infarction NB - the eye that fails to adduct tells you which side the lesion is on
39
What causes vertical nystagmus?
Brainstem lesion - upgaze nystagmus suggests a lesion in the midbrain or upper pons, or Wernicke's encephalopathy - downgaze nystagmus suggests a foramen magnum lesion, cerebellar degeneration or Wernicke's encephalopathy Toxic - e.g. alcohol or pehnytoin
40
What causes pendular nystagmus?
Decreased macular vision, e.g. albinism | Congenital
41
Causes of ptosis with normal pupils
``` Senile ptosis Myasthenia gravis Myotonic dystrophy Facioscapulohumeral dystrophy Ocular myopathy Thyrotoxic myopathy Botulism Snake bite ```
42
Causes of ptosis with constricted and dilated pupils
Constricted pupils - Horner's syndrome, tabes dorsalis | Dilated pupils - 3rd nerve palsy
43
Causes of bilateral ptosis
Midbrain lesion
44
Causes of unilateral proptosis
``` Grave's disease Cavernous sinus thrombosis (associated with chemosis and painful ophthalmoplegia) Carotid-cavernous fistula Tumour (benign or malignant) Capillary haemagnioma Cellulitis of the eye Sarcoidosis Neurofibromatosis ```
45
What causes trigeminal nerve palsy?
Central (pons, medulla and upper cervical cord) - vascular, tumour, syringobulbia (increasing cavitation of the central pons and medulla) Peripheral (posterior fossa) - aneurysm, skull base tumour Trigeminal ganglion (petrous temporal bone, can also affect CN VI in Gradanigo's syndrome) - meningioma, fracture of the middle fossa Cavernous sinus (associated with III, IV and VI palsies) - aneurysm, thrombosis, tumour Other systemic problems - Sjogrens syndrome, SLE
46
Isolated palatal myoclonus would make one think of a lesion in the...
Palatal myoclonus is pathognomonic of hypertrophic olivary degeneration involving a lesion in the triangle of Guillain and Mollaret causing hypertrophy of the inferior olivary nucleus
47
Name some causes of absent ankle jerks and upgoing plantars
This is essentially asking for causes of mixed upper and lower motor neuron signs Subacute combined degeneration of the cord (B12 deficiency causes peripheral neuropathy hence absent ankle jerks, but also damage to the CST causing upgoing plantars) Tabes dorsalis (tertiary syphilis) Freiderich's ataxia Conus medullaris lesion Motor neurone disease (usually wasting and fasciculations + brisk reflexes) Diabetes (peripheral neuropathy + CVA)
48
Give some causes of facial pain
Trigeminal neuralgia (NB exclude multiple sclerosis, meningioma) and post herpetic neuralgia Paratrigeminal syndrome (severe retro-orbital pain with ipsilateral ptosis and meiosis) Superior orbital fissure syndrome (retro-orbital boring pain with paresis of cranial nerves III, IV, V and VI Cluster headaches (severe, focal pain of rapid onset, usually in males with tearing and rhinorrhoea) Temporal arteritis (usually in patients >50 years with an elevated ESR, anaemia, fevers and fatigue). Strong association with PMR Temporomandibular arthritis and diseases of the sinuses, teeth and ears Glaucoma Aneurysm of internal carotid or posterior communicating arteries Atypical facial pain