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50 Cards in this Set

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Anisocoria
-pupils of unequal size
-difference of 0.75 and 1.0 mm is significant
-physiologic will show the same difference in pupil size in dark and bright
Anisocoria greater in bright
problem with iris constrictor -> sign of parasympathetic involvement -> larger pupil is abnormal
Anisocoria greater in dim
problem with dilator -> sign of sympathetic involvement -> smaller pupil is abnormal
Tonic Pupil Syndrome
-anicoria in which one eye is larger in bright light and the other eye is larger in dim light
-parasympathetic and sympathetic involvement
1/8% pilocarpine
-tests to see if pupils are pharmacologically dilated
-for normal px (and those that are pharmacologically fixed), pilo should NOT elicit pupillary response
-px with prior presynaptic nerve damage will have an increased sensitivity to ACH (up-regulation) and pupil will constrict after 30 minutes
Should you do the pilocarpine test on pxs you suspect a 3rd nerve palsy?
NO
5 causes of Light-Near Dissociation
1. Argyll-Roberts (syphilis)
2. Dorsal Midbrain Syndrome
3. Amaurotic eye
4. Tonic pupils
5. Aberrent regeneration
Differential Diagnoses of tonic pupil
-posterior synechia
-acute angle closure glaucoma
-bitemporal sphincter palsy/temporal iris ischemia
-tadpole pupils
Pupil appearance of a tonic pupil
-mid-dilated
-tonic pupil is larger in bright light
-tonic pupil is smaller in dim light
-tonic pupil is light-near dissociated (pupil constricts to accommodation but not to light)
What does bitemporal sphincter palsy look like and what is it caused by?
-vertically oriented pupils
-caused by ischemic ocular syndrome (esp in diabetics) or from ischemia secondary to PRP in diabetics
What are tadpole pupils associated with?
-migraines and sympathetic irritation
-unusual dilation during a headache
-benign condition
3 cardinal signs of a tonic pupil
1. Sector paralysis
2. Stromal spread
3. Stromal streaming
Sector paralysis
-tonic pupil has curved and flattened parts
-flat region is sectors of iris that are paralyzed
-there is loss of tone due to lesion of short posterior ciliary nerves
Stromal Spread
-iris has radial folds bt iris sphincter and dilator muscles
-loss of tone causes stroma to disorganize and surface of iris becomes lax
Stromal Streaming
-damaged iris will stream towards light beam of slit lamp
-when light is on the iris, normal part streams to tighten, but the damaged part does not move at all; may appear to rotate orr go to one side as it constricts
What is the cause of tonic pupils?
-ciliary ganglion is damaged
Edinger Westphal nucleus
-explains light-near dissociation
-3% of fibers from EW go to sphincter muscle for constriction; 90% of fibers from EW are for accommodative function
-Ciliary ganglion gives rise to most of fibers for constriction
-therefore damage to CG and not EW will affect a small portion of accommodative fibers and many more constrictive fibers
-thus, near accommodative ability is left intact
Causes of Tonic Pupils
1. Local tonic pupil caused by infection in the orbit (varicella, retrobulbar masses, PRP, orbital tumor)
2. Neuropathic causes (diabetes is most common cause*, syphilis, sarcoidosis, lyme disease)
3. Idiopathic causes = Adie's tonic pupil
What do you have to rule out before you can call a tonic pupil Adie's?
DM, syphilis, sarcoidosis, Lyme's
Adie's Tonic pupil characteristics
-browache, anisocoria, trouble focusing
-female prevalence
-age 20-40
-**90% unilateral presentation
-fellow eye involvement is common at 4% per yr
What is Adie's Tonic Pupil accompanied by?
-diminished corneal sensitivity
-decreased deep tendon reflexes
Management of Adie's Tonic Pupil
-leave it alone
-if px is experiencing symptoms: homatropine OU to alight near pt and prescribe reading glasses (may need unequal add)
-glasses
-occlusion
-colored contacts
CN III Palsy features
-ptosis
-mid-dilated pupil
***involved pupil = aneurysm
***spared pupil = vasculopathic (DM)
-reduced response to light and near
-external ophthalmoplegia
-complete and incomplete inability to move eye in or up
-pain
Complete or Incomplete CN III palsy
1. Complete & dilated pupil = aneurysm
2. Complete & spared pupil = diabetes
3. Incomplete & dilated pupil = aneurysm
4. Incomplete and spared pupil = CAN'T TELL
Acute onset CN III palsy with pupil involvement
= aneurysm at junction of posterior communicating and internal carotid arteries = EMERGENCY (20f% die within 48 hrs)
Dorsal Midbrain Syndrome
= Parinaud's Syndome = Sylvian Aqueduct Syndrome
-compression from back of midbrain from tumor, CSF obstruction, inflammatory, infection
DMS Signs
-tectal pupils (mid-dilated & dont react well to light but fine for near)
-upgaze paresis
-convergence-retraction nystagmus (bc px cant look up so eyes go in or out)
-eyelid retraction (Collier's sign); eyes cant look up but eyelids can still rise normally
Possible cause of DMS
-pineal gland tumor (just posterior to dorsal midbrain)
-pineal tumor looks like bone on MRI and CT due to calcification
Uncal Syndome
-severe lid retraction
-unable to look up
-light near dissociation
-uncal hernation due to sudden increased ICP shifting cerebral contents
-compression of uncus of temporal lobe compressing the third nerve causes the pupil to become fixed and dilated
-Blown pupil = *Hutchinson Pupil
Horner's dilation lag
anisocoria is greater at 5 seconds than at 12 seconds into darkness; in a normal physiologic/benign essential anisocoria, the pupil is fully dilated at 5 seconds so there is no difference in relative pupil size at 5 seconds and at 12 seconds
Horner's cocaine test
-positive test results in no dilation
-cocaine blocks the reuptake of norepinephrine at the nerve terminal
-normal pxs have a normal amount of norepinephrine, and the blockage by cocaine causes dilation
-horner's pxs have a decreased amount of norepinephrine, and the blockage by cocaine does not do anything; thus the patient does not dilate
Apraclonidine test for Horner's
-potential new diagnostic test
-no effect on normal pupil
-dilates Horners pupil bc it is supersensitive
-OPPOSITE of cocaine test
-look for reversal of anisocoria
Eyelid crease in Horner's vs Myasthenia Gravis
-Horners: eyelid crease is still present bc levator function is normal
-Myasthenia Gravis: CN III disease that causes disinsertion of the tarsal plate; eyelid crease absent bc the levator is affected
Inverse Ptosis
-in Horners, lower lid looks elevated due to inability of inferior muscle of Mueller to pull lower lid down
-presence indicated Horners
-Myasthenia Gravis & CN III palsy do NOT have inverse ptosis
Heterochromia iridis
-stromal melanocytes in iris need sympathetic innervation to mature and give iris its color
-look for lighter iris on side you suspect Horner's
-generally occurs only in congenital Horner's (before age 2)
Ipsilateral straightening of hair
-sympathetic nerve fibers innervate the scalp
-before age 2, for px to have curly hair there must be sympathetic activity in the scalp
-horner's px may have curly hair on one side and straight on the other due to lack of sympathetic innervation
-generally in congenital Horner's
What are two signs of congenital Horner's?
-heterochromia iridis
-ipsilateral straightening of hair
What is the most common cause of Horner's in young patients?
Neuroblastoma
-causes Klumpke's sign (lack of sympathetic innervation to arms and hands; no wrinkling in water) and Gustatory lid retraction (certain neural stimuli such as eating a lemon causes the lid to shoot up and the pupil to dilate)
CN IV palsy & Horner's
-oculosympathetic fibers travel from midbrain to pons at locus ceruleus
-locus ceruleus is ver close to CN IV
-CN IV crosses in midbrain and when lesioned can cause a contralateral Horner's
Foville Syndome & Horner's
-level of pons
-fibers from midbrain travel to caudal pons
-lesion here such as infarct of anterior inferior cerebellar artery can cause Foville syndrome
-infarct of AICA
-CN VI damage
-CN VII palsy (CN VI and VII are next to each other in pons)
-CN VIII palsy
-CN V palsy
Wallenberg Syndrome & Horner's
-oculosympathetic fibers travel from pons to lateral medulla
-infarct here causes Wallenberg Syndrome
-occurs with Horner's intermittent diplopia, contralateral loss of pain and temp, ipsilateral loss of hearing, swallowing and speech difficulties, nystagmus, nausea, ipsilateral ataxia
Phrenic nerve or brachial plexus Syndrome
-at the level of the spinal cord
-mostly associated with female pxs
-associated with metastatic breast cancer
-Triad of phrenic nerve syndrome : hoarse, hiccoughs, and Horner's
What kind of lung tumor is associated with Horner's?
Pancoast's tumor
-fibers at the level of c7-T2 split and travel very close to the apex of lung
-Triad of pancoast tumor: ptosis, miosis, arm pain
Carotid Artery dissection
-px may present with Horner's bc sympathetics travel around carotid plexus
-may also have amauosis fugax, dysgeusia (metallic taste), eye pain
-EMERGENCY
-can lead to stroke, esp in young pxs
-50-95% will have retinal or cerebral ischemia if left untreated
**Triad of Carotid Dissection:
1) pain on side of face, head, or neck
2) oculosympathetic paralysis without anhydrosis
3) delayed retinal or cerebral ischemia
A tumor at the base of the skull that can produce a Horner's is called what?
Vernet's Syndrome
-nasopharyngeal cancer
-px presents with droopy shoulder
-droopy tongue
-winged scapula
-weak trapezius
-hoarse
-tongue deviated to one side
1st, 2nd, and 3rd order neurons
1st- brain to clavicle
2nd- clavicle to mandible
3rd- mandible to eye
Paredrine 1% Test
-located Horner's lesion if it is isolated
-paredrine puts norepinephrine from the presynaptic nerve terminal into the synapse
-if lesion occurs at 3rd order neuron (postganglionic), above the mandible, the pupil will NOT dilate unless the lesion is acute and there has been time to deplete the neurotransmitter
-if the lesions is at the 1st or 2nd order neuron (preganglionic), below the mandible, then the pupil WILL dilate
Causes of Horner's?
1. 40% idiopathic
2. 13% malignant tumor, usually Pancoast
3. Neuroblastoma in children
Rule of thumb localization
1st neuron lesion, think vascular disease or trauma
2nd neuron lesion, think neoplasia
3rd neuron lesion, think benign or headache syndrome
Argyll-Robertson pupils
-miosis, 2.5 mm max in dark
-absent direct response to light
-light near dissociation (normal response to near)
-preserved vision
-unilateral, asymmetric, or unequal
-dilates poorly