Neuro-ophthalmology

Neuro-ophthalmology


Nystagmus












































































































1. Complete the following about nystagmus:


 


G7 p.828:50mm


a. What is nystagmus? i_____ r_____ o_____ of the eyes


involuntary rhythmic oscillation


 


b. What is the most common form?


jerk nystagmus


 


c. How is its directionality defined?


fast component


 


d. What is the abnormal component?


slow component


 


e. What is vertical nystagmus indicative of?


 


 


     i. p_____ f_____ p_____


posterior fossa pathology


 


     ii. s_____


sedatives


 


     iii. a_____ d_____


antiepileptic drugs


 


2. Seesaw nystagmus occurs with a lesion in the_____.


diencephalon


G7 p.828:68mm


3. Nystagmus retractorius occurs with a lesion in the_____ _____ _____; for example p_____.


upper midbrain tegmentum; pinealoma


G7 p.828:83mm


4. Ocular bobbing occurs with a lesion in the_____ _____.


pontine tegmentum


G7 p.828:135mm


5. Matching. Match the form of nystagmus and the location of the lesion. Form: seesaw nystagmus; convergence nystagmus; nystagmus retractorius; downbeat nystagmus; upbeat nystagmus; abducting nystagmus; ocular bobbing Location:


 


G7 p.828: 70mm


a. diencephalon



 


b. upper midbrain tegmentum



 


c. midbrain tectum



 


d. pons medial longitudinal fasciculus (MLF)


,


 


e. medulla



 


f. post-fossa—cervicomedullary junction



 


6. Name the location of the lesion in nystagmus.


 


G7 p.828:70mm


a. seesaw nystagmus


diencephalon


 


b. nystagmus retractorius


upper midbrain tegmentum/pineal region


 


c. downbeat nystagmus


cervicomedullary junction (foramen magnum)


 


d. upbeat nystagmus


medulla


 


e. ocular bobbing


pons


 


Papilledema




































































7. Complete the following about papilledema:


 


G7 p.828:165mm


a. What is papilledema caused by?


Thought to be caused by axoplasmic stasis. Theory: Increase intracranial pressure (ICP) transmitted to the optic disk via subarachnoid (SA) space. Retinal venous pulsations obliterated. Retinal arterial: venous pressure ratio < 1.5:1.


 


b. How long does it take to develop?


24 to 48 hours


 


c. What is the earliest it is seen?


6 hours


 


d. Does it cause visual blurring?


no (unless severe and prolonged)


 


e. Does it cause visual field distortion?


no (unless severe and prolonged)


 


f. Differentiate from optic neuritis.


 


 


     i. funduscopy _____ _____ _____


may look alike


 


     ii. visual lost more with_____ _____


optic neuritis


 


     iii. pain on palpation more with _____ _____


optic neuritis


 


8. What is the differential diagnosis for unilateral papilledema? Hint: Fiom


 


G7 p.829:30mm


a. F_____-_____


Foster-Kennedy


 


b. i_____


inflammation


 


c. o_____ _____ optic glioma


 


d. m_____ _____


multiple sclerosis


 


Pupillary Diameter
































































































































































































9. Complete the following concerning the pupillodilator nerve fibers:


 


G7 p.829:180mm


a. first-order sympathetic nerve fibers


 


 


     i. origin, p_____ h_____


posterolateral hypothalamus


 


     ii. destination, i_____ cell column (_____ to_____)


intermediolateral (C8 to T2)


 


     iii. neurotransmitter, a_____


acetylcholine (ACh)


 


b. second-order sympathetic nerve fibers


 


 


     i. origin, i_____ cell column


intermediolateral


 


     ii. destination, s_____ c_____ g_____


superior cervical ganglion


 


c. third-order sympathetic nerve fibers


 


 


     i. origin, s_____ c_____ g_____


superior cervical ganglion


 


     ii. destination, p_____ m_____ of the eye, l_____ g_____, M_____ m_____


pupillodilator muscle (long ciliary nerves), lacrimal gland, Müller muscle


 


     iii. neurotransmitter, n_____


norepinephrine


 


10. How are pupillodilator muscles arranged?


radially


G7 p.829:180mm


11. Describe the anatomy of sympathetic outflow to the eye. Hint: hilsc


 


G7 p.829:180mm


a. h_____


hypothalamus


 


b. i_____ _____ _____


intermediolateral cell column


 


c. l_____ _____ _____


lateral horn cells


 


d. c_____ _____


ciliary ganglion Sympathetic summary: first order: posterolateral (a) hypothalamus → descend in midbrain tegmentum uncrossed to pons, medulla, spinal cord (SC) to the (b) intermediolateral cell columns, C8-T2 (ciliospinal center of Budge). → synapse with (c) lateral horn cells acetylcholine (ACh) and give off second-order neurons (a) (preganglionics). Second order: enter sympathetic chain → (b) superior cervical ganglion. Third order: (a) (postganglionics): go up with common (b) carotid artery (CCA) those that mediate sweat to face go up external carotid artery (ECA), the rest go up internal carotid artery (ICA). Some pass: = (d) V1 → ciliary ganglion → (e) pupillodilator norepinephrine (NE)= ICA → (f) ophthalmic artery → (g) lacrimal gland and the Müller muscle.


 


12. The pupilloconstrictor (parasympathetic) are muscles arranged c_____ as a s_____.


concentric as a sphincter


G7 p.830:55mm


13. Describe the parasympathetic outflow to the eyes. Hint: Ect


 


G7 p.830:75mm


a. E_____


Edinger-Westphal


 


b. c_____


ciliary ganglion


 


c. t_____


third nerve Parasympathetics summary: Preganglionics arise in the Edinger-Westphal nucleus at the level of the superior colliculus synapse in the ciliary ganglion. Postganglionics travel on the third nerve to (e) innervate sphincter pupillae and ciliary muscle (thickens lens causing accommodation via relaxation).


 


14. Describe the pupillary light reflex.


 


G7 p.830-:75mm


Hint: ropEtcs


 


 


a. r_____


retina


 


b. o_____


optic nerve


 


c. p_____


pretectal


 


d. E_____


Edinger-Westphal


 


e. t_____


third nerve


 


f. c_____


ciliary ganglion


 


g. s_____


sphincter light reflex Summary: Mediated by (a) rods and cones of retina. Transmit via axons to (b) optic nerve (ON). Bypass lateral geniculate body (unlike vision) synapse in (c) pretectal nuclear complex. Connect to both (d) Edinger-Westphal nuclei. Preganglionics travel in (e) third nerve to (f) ciliary ganglion, etc. Cornea rods and cones (retina) axons optic nerve bypass lateral geniculate body pretectal nuclear complex Edinger-Westphal nuclei (both preganglionics) to ciliary ganglion. Postganglionics via third nerve to pupillary sphincter. Ciliary muscles thicken (relax) causing accommodation.


 


15. Complete the following about Argyll Robertson pupil:


 


G7 p.830:140mm


Hint: ALRP = Argyll Robertson


 


 


pupil = absent light response pupil


 


 


a. Key feature is_____ _____ _____ _____or ALRP.


absent light response pupil


 


b. It occurs in_____.


syphilis


 


c. Near light dissociation means the pupil constricts when focusing on an object_____


near


 


d. but the pupil does not react to_____.


light


 


16. In which condition do you have light-near dissociation, that is, an Argyll Robertson pupil?


syphilis


G7 p.830:140mm


17. Complete the following about Argyll Robertson pupil:


 


G7 p.830:135mm


a. Light-near dissociation refers to pupillary_____


constriction


 


b. on convergence and_____ of papillary constriction to shining of the light into the eye


absence


 


c. classically described in_____


syphilis


 


d. also known as_____ _____ _____


Argyll Robertson pupil


 


Hint: prostitutes principle, “They accommodate but don’t react.”


 


 


Alterations in Pupillary Diameter
















































































































































































































18. Does afferent pupillary defect cause anisocoria?


no


G7 p.831:25mm


19. Complete the following about anisocoria:


 


G7 p.831:25mm


a. Unequal pupils with an affarent pupillary defect (Marcus-Gunn) means there are_____ _____.


two lesions


 


b. Physiologic anisocoria occurs in_____% of people.


20%


 


c. The difference is usually_____ mm.


0.4


 


d. Sudden onset of anisocoria is usually due to_____.


drugs


 


e. Sympathomimetics cause_____ to_____ mm of dilation and


1 to 2


 


f.


 


 


     i. parasympatholytics cause_____ mm of dilation and the


8


 


     ii. eye_____ _____ react to light.


does not


 


20. Complete the following about Horner syndrome:


 


G7 p.831:100mm


a. The abnormal pupil is_____.


smaller


 


b. Ptosis is on the side of the_____ pupil.


small


 


21. With third nerve palsy, if there is ptosis it will be on the side of the_____ pupil.


large


G7 p.831:110mm


22. Complete the following about oculomotor neuropathy:


 


G7 p.831:116mm


a. Example is_____


diabetes


 


b. Usually_____ the pupil


spares


 


c. Usually resolves in_____ _____


8 weeks


 


23. Complete the following about third nerve compression:


 


G7 p.831:121mm


a. Example is_____


aneurysm


 


b. Most common is_____


P-comm


 


c. Occasionally_____ _____ aneurysm


basilar bifurcation


 


d. Usually_____ _____ _____ the pupil


does not spare


 


24. What is the differential diagnosis of anisocoria?


 


G7 p.831:38mm


Hint: u tAp Hat


 


 


a. u_____


uncal herniation (also has mental status changes)


 


b. t_____


trauma (traumatic iridoplegia mydriasis or miosis)


 


c. A_____


Adie pupil (iris palsy— impaired postganglionic parasympathetics)


 


d. p_____


physiologic (less than 1 mm difference—20% of population)


 


e. H_____


Horner syndrome (impaired sympathetics to pupillodilator muscle)


 


f. a_____


aneurysm (posterior communicating, basilar)


 


g. t_____


third nerve palsy (pupil sparing-diabetes mellitus [DM 1], ETOH, cavernous aneurysm)


 


25. What is the differential diagnosis for Marcus-Gunn pupil?


 


G7 p.831:170mm


a. Location of lesion_____


ipsilateral to impaired direct reflex anterior to chiasm


 


     i. r_____ —d_____ i_____


retina—detachment, infarction


 


     ii. n_____ —m_____ s_____, v_____, or t_____


nerve—neuritis, multiple sclerosis (MS, viral)—trauma


 


b. In Marcus Gunn is/are the


 


 


     i. third nerve intact?


yes


 


     ii. parasympathetic nerves intact?


yes


 


26. Complete the following about Adie pupil:


 


G7 p.832:40mm


a. An Adie pupil is an_____palsy resulting


iris


 


b. in a_____ pupil, due to


dilated


 


c. impaired_____ _____.


postganglionic parasympathetics


 


d. Clinically, patients exhibit_____-_____ _____.


light-near dissociation


 


e. Typically it occurs in a_____ in her_____.


woman; twenties


 


27. The patient with an Adie pupil has a


 


G7 p.832:45mm


a. dilated or constricted pupil?


dilated


 


b. due to impaired preganglionic fibers or postganglionic fibers?


postganglionic


 


c. thought to be caused by a_____ _____


viral infection


 


d. of the_____ _____


ciliary ganglion


 


Horner Syndrome
































































































































28. Horner syndrome is caused by interruption of sympathetics to the eye and face anywhere along their path. Name specific causes that affect the following:


 


G7 p.833:80mm


a. first-order neurons (three causes)


 


 


     i. i_____


infarction from vascular occlusion (usually posterior inferior cerebellar artery)


 


     ii. s_____


syringobulbia


 


     iii. i_____ n_____


intraparenchymal neoplasm


 


b. second-order neurons (three causes)


 


 


     i. l_____ s_____


lateral sympathectomies


 


     ii. s_____ c_____ t_____


significant chest trauma,


 


     iii. a_____ p_____ n_____ (P_____ t_____)


apical pulmonary neoplasms(Pancoast tumor)


 


c. third-order neurons (five causes)


 


 


     i. n_____ t_____


neck trauma (e.g., carotid dissections)


 


     ii. c_____ v_____ d_____


carotid vascular disease


 


     iii. c_____ b_____ a_____


cervical bony abnormalities


 


     iv. m_____


migraine


 


     v. sk_____ -b_____ n_____


skull-base neoplasms


 


29. The ptosis is due to paralysis of the_____ and _____ _____muscles.


superior and inferior tarsal


G7 p.833:80mm


30. Is the ptosis complete or partial?


partial


G7 p.833:80mm


31. Enophthalmos is due to paralysis of M_____ muscle, which is or is not involved in Horner syndrome?


Müller muscle; is involved


G7 p.833:89mm


32. Trace the third-order neuron in the pupillodilation/sympathetic path. Neurons from the s_____ c_____ g_____ to the p_____ m_____ and M_____ m_____.


superior cervical ganglion to the pupillodilator muscle and Müller muscle


G7 p.833:125mm


33. True or False. Answer the following regarding Horner syndrome:


 


G7 p.833:125mm


a. In a patient with Horner syndrome and preserved sweating of the face, the lesion is located


 


G7 p.833:125mm


     i. in the first-order neuron


false


 


     ii. in the second-order neuron


false


 


     iii. in the third-order neuron


true (Injured fibers on ICA produce Horner, intact sweat fibers to face on ECA.)


 


b. This is compatible with a Pancoast tumor.


false (Pancoast tumor would affect the sympathetics between the spinal cord and superior cervical ganglion [i. e., second-order neurons]. The fibers to sweat glands would be damaged because they had not yet separated to travel with the ECA.)


 


34. Complete the following about Horner syndrome:


 


G7 p.833:160mm


a. What medication is used if diagnosis of Horner syndrome is in doubt?


cocaine


 


b. How does it work?


cocaine blocks norepinephrine (NE) reuptake


 


c. Therefore in Horner syndrome the pupil will_____.


not dilate with cocaine (there is no NE release)


 


d. In a normal patient the pupil will_____.


dilate normally


 


Extraocular Motor System
















































































































































































































































































































































35. Matching. From the list below identify the cranial nerve that innervates the muscle.


 


G7 p.834:45mm


Nerve:


 


 


III; IV; VI Hint: L6 SO4


 


 


Muscle:


 


 


a. medial rectus



 


b. inferior rectus



 


c. inferior oblique



 


d. superior rectus



 


e. superior oblique



 


f. lateral rectus



 


36. Complete the following regarding the frontal eye field:


 


G7 p.834:52mm


a. True or False. It moves eyes laterally to the opposite side.


true


 


b. It is located in the Brodmann area_____.


8


 


c. Its fibers go through the_____ of the_____ _____.


genu of the internal capsule


 


d. It sends fibers to the ipsilateral_____ _____ _____ nucleus.


paramedian pontine reticular formation (PPRF)


 


e. It sends fibers to the ipsilateral_____ nucleus


sixth


 


f. and the contralateral_____ nucleus


third


 


g. via the_____ _____ _____.


medial longitudinal fasciculus (MLF)


 


h. The right paramedian pontine reticular formation (PPRF) controls lateral eye movements to the_____.


right


 


37. Complete the following about the extraocular motor system:


 


G7 p.834:90mm


a. Injury to the medial longitudinal fasciculus (MLF) is called_______.


internuclear ophthalmoplegia (INO)


 


b. Convergence is_____ _____.


not impaired


 


c. If the right MLF is injured the right eye will not_____ _____.


move medially (adduct)


 


d. The left eye on looking laterally shows


 


 


     i. w_____ _____ a_____


weakness on abduction


 


     ii. n_____ or adduction.


nystagmus


 


e. The most common cause of MLF malfunction is_____ _____.


multiple sclerosis (MS)


 


38. Name three causes of non-pupil-sparing oculomotor palsy.


 


G7 p.835:40mm


Hint: tau


 


 


a. t_____


tumor


 


b. a_____


aneurysm (posterior communicating artery, basilar tip)


 


c. u_____


uncal herniation


 


39. Name seven causes of pupil-sparing oculomotor palsy.


 


G7 p.835:100mm


Hint: mEtDacc


 


 


a. m_____


myasthenia gravis


 


b. E_____


ETOH


 


c. t_____


temporal arteritis


 


d. D_____


DM


 


e. a_____


atherosclerosis


 


f. c_____ _____ _____


chronic progressive ophthalmoplegia


 


g. c_____ _____ _____


cavernous sinus lesions


 


40. Complete the following about trochlear nerve palsy (IV):


 


G7 p.835:160mm


a.


 


 


     i. In relation to the aqueduct the trochlear nucleus lies_____


ventral


 


     ii. At the level of the_____ _____


inferior colliculi


 


b.


 


 


     i. The axons pass_____


dorsally


 


     ii. Decussate_____


internally


 


c. It innervates the_____ _____ muscle


superior oblique


 


d. The superior oblique muscle


 


 


     i. Which primarily depresses the_____ eye?


adducted


 


     ii. In primary gaze it moves the eye_____ and_____.


down and out


 


41. Complete the following about the unique features of the trochlear nerve:


 


G7 p.835:172mm


a. Nucleus is on the_____ side of the


opposite


 


b. muscle it goes to:_____ _____ _____.


superior oblique muscle


 


c. It is the only nerve to decussate_____.


internally


 


d. It is the only nerve to exit_____ to the brain stem.


posterior


 


e. True or false. It passes through the annulusof Zinn.


false


 


f. Palsy results in eye deviation_____ and_____.


up and in


G7 p.836:18mm


g. Head is tilted to the_____ the IV palsy.


side opposite


 


h. Diplopia is exacerbated when looking_____ (i.e.,_____).


down; stairs


 


42. Name the causes of abducens palsy.


 


G7 p.836:45mm


Hint: abducens


 


 


a. a_____


arteritis, aneurysms


 


b. b_____


sixth nerve palsy


 


c. d_____


diabetes, Dorello canal (Gradenigo syndrome)


 


d. u_____


uncontrolled ICP, pseudotumor, trauma, tumor


 


e. c_____


cavernous sinus lesions, clivus, chordoma, or fracture


 


f. e_____


eye disease, thyroid, myasthenia gravis


 


g. n_____


neoplasms


 


h. s_____


sphenoid sinusitis (Gradenigo syndrome)


 


43. Matching. Match the syndrome with the nerves involved in multiple extraocular motor involvement.


 


G7 p.836:125mm


Syndrome:


 


 


cavernous sinus; superior orbital fissure; orbital apex


 


 


Nerves involved:


 


 


a. II



 


b. III


, ,


 


c. IV


, ,


 


d. V1


, ,


 


e. V2



 


f. V3


 


 


g. VI


, ,


 


Tolosa-Hunt Syndrome
























































































































































44. Is the ophthalmoplegia painful or painless?


painful


G7 p.837:175mm


45. Which nerve(s) is/are involved?


any nerve traversing the cavernous sinus


G7 p.837:175mm


46. The pupil is usually_____.


spared


G7 p.837:175mm


47. How long do symptoms last?


days to weeks


G7 p.837:175mm


48. Can there be spontaneous remission?


yes


G7 p.837:175mm


49. Can there be recurrent attacks?


yes


G7 p.837:175mm


50. Is there systemic involvement?


no


G7 p.837:175mm


51. How is it treated?


systemic steroids = 60 to 80 mg prednisone by mouth daily (slow taper)


G7 p.837:175mm


52. The disease is thought to be a_____ _____.


nonspecific inflammation


G7 p.837:175mm


53. The inflammation is located at the_____ _____ _____.


superior orbital fissure


G7 p.837:175mm


54. Complete the following about Raeder paratrigeminal neuralgia:


 


G7 p.838:50mm


a. Name two components.


 


 


     i. u_____ o_____ p_____


unilateral oculosympathetic paresis (think Horner syndrome—anhidrosis ± ptosis)


 


     ii. h_____ t_____ n_____ i_____


homolateral trigeminal nerve involvement (Horner syndrome and tic-like pain)


 


b. The pupil is_____


small


 


c. True or False. The pain is continuous.


false (intermittent, tic-like)


 


d. The pain is located at the_____.


trigeminal nerve V1 (ophthalmic division) and sympathetics


 


55. Complete the following regarding Gradenigo syndrome:


 


G7 p.838:85mm


a. Name the classic triad.


 


 


     i. p_____ of_____


palsy; abducens


 


     ii. p_____ where?_____


pain; retro-orbital


 


     iii. d_____ e_____


draining ear


 


b. Pain is located at the p_____ a_____.


petrous apex


 


56. Complete the following about Gradenigo syndrome:


 


G7 p.838:85mm


a. What is Gradenigo syndrome?


apical petrositis


 


b. Involves_____ canal


Dorello


 


c. Features


 


 


     i. G_____


Gradenigo


 


     ii. r_____


retro-orbital pain


 


     iii. a_____ _____


apical petrositis—abducens palsy


 


     iv. d_____ _____


draining ear—Dorello canal ear draining


 


     v. e_____ _____


ear draining


 


     vi. n_____ _____ _____


neuropathy of VI


 


     vii. i_____


inflammation


 


     viii. p_____


petrositis


 


     ix. o_____ p_____


orbital pain


 


Miscellaneous Neuro-ophthalmologic Signs































57. Complete the following about ocular bobbing:


 


G7 p.838:165mm


a. The eyes move_____.


downward


 


b. How many times per minute?


2 to 12


 


c. Ocular bobbing is associated with bilateral paralysis of_____ _____.


horizontal gaze


 


d. It is seen with destruction of the_____ _____.


pontine tegmentum


 


58. Optic atrophy is due to a_____ lesion.


compressive


G7 p.839:45mm


Stay updated, free articles. Join our Telegram channel

Aug 6, 2016 | Posted by in NEUROSURGERY | Comments Off on Neuro-ophthalmology

Full access? Get Clinical Tree

Get Clinical Tree app for offline access