Syndromes Flashcards

1
Q

Dorsal cord syndrome

A

Bilateral involvement of dorsal columns, corticospinal tracts, and descending central autonomic tracts to bladder control centers in sacral cord.

  • gait ataxia
  • corticospinal tract –> weakness
    • acute = muscle flaccidity and hyporeflexia
    • chronic = hypertonia and hyperreflexia
  • extensor plantar responses and urinary incontinence may be present

Causes

  • MS
  • tabes dorsalis
  • friedrich ataxia
  • subacute combined degeneration
  • vascular malformation
  • epidural and intradural extramedullary tumours
  • cervical spondylotic myelopathy
  • atlantoaxial subluxation
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2
Q

Ventral cord or anterior spinal artery syndrome

A

Tracts in anterior 2/3 of spinal cord:

  • corticospinal tracts
  • spinothalamic tracts
  • descending autonomic tracts to sacral centers for bladder control
  • weakness and reflex changes
  • bilateral loss of pain and temperature sensation
  • tactile, position and vibratory sensation NORMAL
  • urinary incontinence usually present

Causes

  • spinal cord infarction
  • intervertebral disc herniation
  • radiation myelopathy
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3
Q

Transverse myelitis

A

Bilateral leg weakness
Loss of voluntary control of bladder
Diminished sensation of all modalities
Tight banding sensation around trunk, tenderness

Recent gastro
MS

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4
Q

Cord segmental syndrome

A

Eg acute transection

  • spinal shock with flaccid paralysis
  • urinary retention
  • diminished tendon reflexes

then progression to hypertonia, spasticity and hyperreflexia over days to weeks

Above C3 –> cessation of respiration, usually fatal
Above L2 –> impotence, spastic paralysis of bladder, loss of voluntary control and emptying by reflex action

Causes

  • acute myelopathies such as traumatic injury and spinal cord haemorrhage
  • epidural or intramedullary tumours, abscess
  • transverse myelitis
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5
Q

Brown Sequard Syndrome

A

Lateral hemisection syndrome

Involves dorsal column, corticospinal tract, and spinothalamic tract unilaterally

  • weakness, loss of vibration and proprioception IPSILATERAL to lesion
  • loss of pain and temperature CONTRALATERAL to lesion
  • unilateral involvement of autonomic fibers doesn’t produce bladder symptoms

Causes

  • being stabbed in the back
  • or shot
  • demyelination
  • rarely: spinal cord tumours, disc herniation, infarction, and infection
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6
Q

Central cord syndrome

A
  • loss of pain and temperature sensation in the distribution of one or several adjacent dermatomes at the site of the spinal cord lesion caused by disruption of crossing spinothalamic fibers in the ventral commissure
  • dermatomes above and below have normal pain and temperature sensation - “suspended sensory level”
  • vibration and proprioception often spared
  • may produce weakness in analgesic areas as the lesion enlarges and encroaches on corticospinal tracts
  • loss of tendon reflexes in analgesic areas
  • no bladder symptoms

Causes

  • slow-growing lesions eg syringomyelia or intramedullary tumour
  • most frequently the result of a hyperextension injury in patient with long-standing cervical spondylosis –> this results in disproportionately greater motor impairment in UL > LL, bladder dysfunction, and variable degree of sensory loss below level of injury
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7
Q

Conus medullaris syndrome

A
  • L2
  • early and prominent sphincter dysfunction with flaccid paralysis of bladder and rectum, impotence, and saddle anaesthesia
  • leg muscle weakness may be mild if lesion very restricted

Causes

  • disc herniation
  • spinal fracture
  • tumours
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8
Q

Cauda Equina Syndrome

A
  • Not truly a spinal cord syndrome
  • loss of function of two or more of the 18 nerve roots constituting the cauda equina
  • deficits usually involve both legs, but often asymmetric
  • back pain
  • sciatica
  • change in sensation and weakness in LLs
  • urinary incontinence
  • bowel dysfunction
  • sexual dysfunction (impotence)
  • decreased or absent reflexes in LLs
  • saddle anaesthesia
  • hypotonia/atrophy of LLs
  • decreased or absent rectal tone
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9
Q

Ramsay Hunt Syndrome

A

HSV infection within dermatomal distribution of one of the branches of the trigeminal nerve

  • vertigo
  • +/- hearing loss
  • ipsilateral facial paralysis
  • ear pain
  • vesicles in auditory canal and auricle
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10
Q

Vestibular neuronitis vs labyrinthitis

A

Both:

  • rapid onset
  • severe, persistent vertigo
  • nausea and vomiting
  • gait abnormality
  • spontaneous nystagmus
  • positive head impulse test
  • gait instability with preservation of ambulation

Labyrinthitis only:
- unilateral hearing loss

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11
Q

Wallenberg syndrome

A

AKA lateral medullary infarction, PICA syndrome (posterior inferior cerebellar artery), vertebral artery syndrome

  • acute onset vertigo + disequilibrium
  • infarction of ipsilateral posterior inferior cerebellar artery (or obstruction of the vertebral artery from which it arises)
  • vertigo is main feature but may also get:
  • abnormal eye movements
  • ipsilateral horner syndrome
  • ipsilateral limb ataxia
  • dissociated sensory loss (loss of pain and temp on ipsilateral face and contralateral trunk with preserved vibration and position sense)
  • hoarseness and dysphagia

Can also occur due to traumatic vertebral artery dissection

MRI establishes diagnosis; MRA assesses for dissection

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12
Q

Horner Syndrome

A

Ipsilateral

  • miosis
  • partial ptosis
  • anhydrosis
  • enophthalmos (inset eyeball)
Causes
Central (with anhidrosis of face, arm, trunk)
- syringomyelia
- MS
- encephalitis
- brain tumours
- lateral medullary syndrome

Preganglionic (anhidrosis of face)

  • cervical rib
  • thyroid carcinoma, thyroidectomy
  • bronchogenic carcinoma (Pancoast tumour)
  • thoracic aortic aneurysm
  • trauma or surgery

Postganglionic (no anhidrosis)

  • cluster headache
  • carotid artery dissection/aneurysm
  • cavernous sinus thrombosis
  • middle ear infection
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13
Q

Neuroleptic malignant syndrome

A
  • Association with drugs that block dopamine signalling (neuroleptics, antiemetics etc) and a tetrad of clinical features:
  1. fever
  2. rigidity
  3. mental status changes
  4. dysautonomia

Mostly starts with mental status changes –> rigidity, hyperthermia, autonomic dysfunction.

NB - CK elevation 4x normal

SNS lability - BP fluctuation/elevation, diaphoresis, urinary incontinence
Hypermetabolism, HR increase, RR increase

Specific treatments = dantrolene, bromocriptine, ECT

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14
Q

Serotonin Syndrome

A

Classic triad =

  1. mental status changes
  2. autonomic hyperactivity
  3. neuromuscular abnormalities

HUNTER CRITERIA
Patient must have taken serotonergic agent and meet ONE of the following:
- spontaneous clonus
- inducible clonus PLUS agitation or diaphoresis
- ocular clonus PLUS agitation or diaphoresis
- tremor PLUS hyperreflexia
- hypertonia PLUS temperature > 38 PLUS ocular clonus or inducible clonus

(84% sensitive, 97% specific)

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15
Q

Cholinergic syndrome

A
Agitation
CNS depression
Coma 
Convulsions
Seizures
Fasciculations and muscle weakness
Bradycardia
Bronchoconstriction and bronchorrhoea
D&V
lacrimation
miosis 
salivation
urinary incontinence
nicotinic:
- HTN
- mydriasis
- sweating
- tachycardia 
(note paradox with muscarinic effects)
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16
Q

Lactrodectism

A
  • Redback spider bite
  • Intense local pain develops after 5-10minutes after bite
  • sweating and piloerection within an hour

pain typically radiates proximally from bite site –> regional –> general

autonomic features: severe sweating (regional or generalised), mild HTN, tachycardia

17
Q

Funnel web spider envenomation

A

Due to an agent that prevents inactivation of sodium channels causing massive increase in autonomic activity and neuromuscular excitation

  • agitation
  • headache
  • vomiting
  • sweating
  • lacrimation
  • salivation
  • HTN
  • tachycardia
18
Q

Tumour lysis syndrome

A
  • hyperkalaemia
  • hyperphosphataemia
  • hypocalcaemia
  • hyperuricaemia
  • high creatinine + urea consistent with renal impairment
  • low HCO3 consistent with metabolic acidosis +/- hyperlactaemia
  • high LDH
19
Q

DIC bloods

A
  • anaemia
  • prolonged APTT, INR, PT
  • thrombocytopaenia
  • low fibrinogen
  • fragmented RBCs on blood film
  • high D dimer
20
Q

Complications in SAH

A
  • rebleeding
    (avoid HTN, avoid decreases in ICP, sedation in the agitated, no coughing or valsalva, antifibrinolytic agents decrease rebleeding by increase vasospasm and hydrocephalus so not used)
  • hydrocephalus
    (EVD)
  • vasospasm
    (prevention - nimodipine 60mg q4h PO, or 1mg/hr IVI)
  • seizures
  • SIADH