CN I: Olfactory Nerve
A deficit in CN I suggests: smoker, trauma, Kallman syndrome, tumor involving the cribriform plate, nasopharyngeal carcinoma, etc.
CN II: Optic Nerve.
1. Bitemporal hemianopia: lesion at optic chiasm
a. tumor
b. craniopharyngioma
c. acromegaly
d. hypopituitarism
e. meningioma
f. suprasellar lesions
g. aneurysm
h. trauma
i. optic nerve glioma
j. infiltrate with granuloma
2. Bi nasal hemianopia:
3. Homonymous hemianopia: lesion in optic tract or optic radiation +/- macular sparing.
a. CVA/stroke (look for ipsilateral hemiplegia, afib, heart murmur, hypertension)
b. tumor
c. occipital pole: macular involvement
4. upper quadrantopia: temporal lobe
5. lower quadrantopia: parietal lobe
6. Altitudinal defect: ischemic optic neuropathy
7. bilateral central scotoma: toxic optic neuropathy
8. tunnel vision: retinitis pigmentosa, glaucoma, thyroid, drusen, vit A defic, occipital stroke, panretinal photocoagulation
OPTIC NERVE LESION
(begins as central or paracentral scotomata, unilateral blindness, loss of pupil reflex)1. optic and retrobulbar neuritis
2. optic nerve compression (tumor/aneurysm)
3. toxic optic neuropathy (tobacco, ethambutol, methyl alcohol, quinine)
4. syphilis
5. ischemic optic neuropathy ( giant cell arteritis)
6. hereditary optic neuropathy
7. severe anemia
8. vitamin B12 deficiency
9. trauma
10. infective (paranasal sinus/orbital cellulitis)
11. papilloedema
12. bone disease in optic canal
Optic Disk Swelling (papilloedema)
1. raised intracranial pressure
-tumor, abscess, hematoma, ICH, SAH, idiopathic htn, hydroceph, enceph
2. optic nerve disease
-optic neuritis, hereditary optic neuropathy, ischemic optic neuropathy, toxic
3. venous occlusion
-cavernous sinus thrombosis, CRVO, orbital mass
4. retinal vascular disease
-malignant hypertension, vasculitis (SLE)
5. metabolic
-hypercapnia, chronic hypoxia, hypocalcemia
6. infiltrate
-leukemia, sarcoidosis, optic nerve glioma
CN III Oculomotor Nerve:
1.eye is down and out due to the fact that only lateral rectus VI (out) and superor oblique IV (down) are functioning. Superior oblique intorts. If CN IV intact then the superior oblique intorts when the patient tries to converge and look down.
2. There is also loss of accommodation (fixed ) ciliary muscle
3. Loss of pupillary reflex : eye is dilated. paralysis of constrictor pupillae
4. in diabetes the pupil is spared and reacts normally to light. (parasympathetic fibers undamaged)
5. there is COMPLETE UNILATERAL PTOSIS. levator palpebrae superioris
6. diplopia may not be evident until the eyelid is lifted.
CAUSES OF A CN III lesion
1. aneurysm posterior communicating artery
2. coning of the temporal lobe uncus
3. CN III infarction (diabetes), (atheroma) nb diabetes usu recovers in 3 months
4. hypertension
5. midbrain infarction
6. midbrain tumor
7. Multiple Sclerosis
8. collagen vascular disorders: giant cell (temporal) arteritis
9. syphilis
10. ophthalmoplegic migraine
11. encephalitis
12. parasellar neoplasms
13. meningioma at sphenoid wing
14. basal meningitis
15. carcinoma at skull base
DIFFERENTIAL (ptosis, dilated pupil, diplopia, lateral gaze)
1. myasthenia
2. thyroid eye disease
UNILATERAL PTOSIS differential
1. third nerve palsy (complete)
2. Horners (partial)
3. myasthenia
4. congenital/idiopathic
BILATERAl PTOSIS
1. myasthenia
2. dystrophica myotonica
3. ocular myopathy/oculopharyngeal dystrophy
4. mitochondrial dystrophy
5. tabes
6. congenital
7. bilateral Horners (syringomyelia)
HISTORY OF CN III lesion.
1. diplopia in all directions except to side of third nerve lesion because lateral rectus intact
2. painful onset eg berry aneurysm or carotid artery aneurysm
3. headache (migraine, cranial arteritis)
4. diabetes
5. hypertension
INVESTIGATION OF CN III LESION
blood pressure
urinalysis:sugar
ESR in elderly patient for GCA
edrophonium test
TFT, orbital US to exclude thyroid dz.
CT head
arteriography if pupil involved and pain
CN II and CN III: Pupil Reflexes:
The pupil reflex arc involves CN II for afferent information, send via the lateral geniculate
without a synapse to the pretectal nucleus on the ispilateral side, synapse and decussation to
both Edinger Westphal nuclei, with afferent limb sent to ciliary ganglion from each EW nucleus
with a synapse in the ciliary ganglion. There are three synapses in the loop.
nb neuroanatomy:
the superior colliculus is in the roof of the midbrain
the most rostral nucleus is the edinger westphal nucleus (superior colliculus)
the pretectal nucleus is caudal (inferior colliculus)
Afferent Pupil Defect
completely blind eye. loss of direct and consensual reflexes (afferent limbs)
affected eye is larger than the other
RAPD: Relative Afferent Pupil Defect, aka Marcus Gunn Pupil.
incomplete damage to afferent limb, eg optic neuritis, retina
not seen with opacities of cornea, lens or with cataracts.
Horner's syndrome (miosis, anhidrosis, ptosis, enophthalmos)
damage to sympathetic pathway
nb.ptosis is usually partial.
nb a third nerve palsy results in a DILATED pupil.
nb the light reflex is intact
if extraocular movements are involved this suggests third nerve palsy or myasthenia)
loss of sweating depends on lesion location.
central lesion: no sweating on entire half head, arm, upper trunk
neck lesion proximal to superior cervical ganglion: decreased facial sweating
lesion distal to superior cervical ganglion: no sweating loss
A lesion distal to superior cervical ganglion: dilates with 1:1000 epinephrine
whereas a normal or proximal lesion does not (due to denervation hypersensitivity of distal lesion)
CAUSES OF HORNERS
hemisphere/brainstem:
1. cerebral infarction (massive)
2. pontine glioma
3. lateral medullary syndrome
4. coning of the temporal lobe (uncus) compressing CN III.
cervical cord
1. syringomyelia
2. cord tumors
sympathetic chain
1. post thyroid/laryngeal surgery
2. carotid artery occlusion/dissection
3. neoplastic infiltrate
4. cervical sympathectomy
T1 root
1. apical bronchial neoplasm
2. apical tuberculosis
3. cervical rib
4. brachial plexus trauma
miscellaneous
1. congenital
2. migrainous neuralgia
3. isolated and unknown cause
the following are not causes of a Horner's
1. diabetes
2. posterior communicating aneurysm
3. increased ICP
4. bells palsy
Arygyll Robertson Pupil (accommodates but does not react, aka light near dissociation)
damage to pretectal nucleus eg due to syphilis.
dorsal midbrain
small irregular pupils
Myotonic Holmes Adie pupil
young adults, female to male 2:1, usually unilateral
enlarged, poorly reactive to light, clow miosis on accommodation
constricts to pilocarpine (supersensitive)
associated with loss of tendon reflexes, eg patellar tendon
Dorsal Midbrain Pupil
1. mydriasis
2. light near dissociation (Argyll Robertson)
3. periaqueductal syndrome (Parinaud): deficient elevation of eyes
CAUSES DORSAL MIDBRAIN PUPIL
a. demyelination
b. pinealoma pressing on tectum
c. infarction of midbrain
d. enlarged 3rd ventricles
Uncal Herniation (herniation of the uncus of the temporal lobe, compressing CN III)
1. ipsilateral hemiparesis
2. fixed and dilated, down and out, ptosis
3. contralateral homonymous hemianopia
CAUSES: usually subdural/extradural hematoma.
Fixed and Dilated Pupil unilateral
1. compression of CN III temporal lobe uncal herniation
2. aneurysm (droopy lid and double vision)
3. eyedrops
4. motion sickness drugs
5. lesion of ciliary ganglion (Adies)
Fixed and dilated pupils (bilateral)
1. brainstem death
2. barbiturate or hypothermic coma
Hutchison Pupil
rapidly rising inracranial pressure
intracerebral hemorrhage
pupil on same side constricts then dilates
opposite pupil then follows same pattern
Bilateral midpoint reactive pupils (normal)
1. metabolic comas, CNS depressants, NOT opiates
Bilateral pinpoint, fixed pupils
1. pontine lesions
2. interruption of sympathetic paths
3. opiates
CN IV Trochlear Nerve
lesion: eye cannot come down and in.
CN VI Abducens Nerve
1. eye cannot abduct.
2. CN VI palsy does not cause nystagmus.
INO: Internuclear Ophthalmoplegia:
Affecting the MLF between the PPRF and the Cn III nucleus.
on lateral gaze, the ipsilateral eye cannot adduct on the side of the lesion and the eye opposite shows nystagmus on abduction.
nb convergence remains intact
Lateral gaze abnormality
destructive lesion: drives gaze towards lesion side
irritative lesoin: drives gaze away from lesion
CN V Trigeminal Nerve
Trigeminal Neuralgia (tic douloureux)
unknown cause
usually old age
usually unilateral
severe paroxysms of knife like/shock like pain in CN V distribution
starts in mandibular travels to maxillary and ophthalmic.
paroxysm stereotyped, trigger zone, stimuli
not at night
recurrence inevitable
no signs
corneal reflex normal
rx: carbamazepine 600-1200 mg daily
surgery: RF ablation, sectioning, alcohol injection.
SECONDARY trigeminal neuralgia.
physical signs present. depressed corneal reflex with trigeminal sensory loss.
1. MS
2. fith nerve neuromas
3. cerebellopontine angle tumors