- •Contents
- •Foreword
- •Preface
- •Acknowledgements
- •1 When ocular disease is mistaken for neurologic disease
- •Double images
- •What important piece of historical information is still missing in this case?
- •Diagnosis: Monocular diplopia due to cataract
- •Headache and bilateral disc edema
- •What test was done and what was the diagnosis?
- •Diagnosis: Malignant hypertension
- •Chronic optic neuropathy
- •Diagnosis: Glaucomatous optic neuropathy
- •Painful mydriasis
- •What clues suggest an alternative diagnosis?
- •Diagnosis: Acute angle closure glaucoma
- •Invisible retinal disease
- •Twinkling scotoma
- •What aspect of this patient’s positive visual phenomenon is highly atypical for migraine?
- •Diagnosis: Acute idiopathic blindspot enlargement
- •Sudden monocular visual loss with normal fundus
- •Hazy night vision
- •Diagnosis: Hypovitaminosis A
- •Swirling vision
- •Diagnosis: Cancer-associated retinopathy
- •Episodic monocular blur
- •FURTHER READING
- •Monocular diplopia
- •Hypertensive retinopathy
- •Twinkling scotoma
- •Central retinal artery occlusion
- •Hypovitaminosis A
- •Cancer-associated retinopathy
- •Corneal decompensation
- •Glaucoma
- •2 When orbital disease is mistaken for neurologic disease
- •Painless vertical diplopia
- •Diagnosis: Euthyroid Graves’ disease
- •Fatigable ptosis
- •How is lid fatigability objectively demonstrated?
- •Diagnosis: Levator dehiscence
- •Painful ptosis and diplopia
- •The investigation thus far has revealed no intracranial pathology. How would you proceed?
- •Painful optic neuropathy
- •Is this patient’s clinical course consistent with a diagnosis of optic neuritis?
- •Diagnosis: Idiopathic optic perineuritis
- •FURTHER READING
- •Orbital examination and restrictive orbitopathy
- •Levator dehiscence
- •Painful ptosis and diplopia
- •Optic perineuritis
- •3 Mistaking congenital anomalies for acquired disease
- •Headaches and elevated discs
- •Are there clues to the correct diagnosis in this case?
- •Diagnosis: Superior segmental hypoplasia
- •Diagnosis: Type I Duane’s syndrome
- •Intermittent vertical diplopia
- •What other causes of fourth nerve palsy should be considered?
- •How would you pursue a diagnosis of congenital fourth nerve palsy in this patient?
- •Diagnosis: Congenital fourth nerve palsy
- •FURTHER READING
- •Pseudopapilledema
- •Superior segmental hypoplasia
- •Duane’s syndrome
- •Congenital superior oblique palsy
- •4 Radiographic errors
- •Ordering the wrong scan
- •Progressive optic neuropathy
- •Is there a problem with the diagnosis of “chronic optic neuritis”?
- •What clinical features in this case suggest the likely mechanism of her chronic optic neuropathy?
- •What additional radiographic evaluation should be obtained?
- •Headache and papilledema
- •Diagnosis: Cerebral venous sinus thrombosis
- •Idiopathic ptosis and miosis
- •Why is the current study incomplete?
- •Diagnosis: Postganglionic Horner syndrome
- •Diagnosis: Internal carotid artery dissection
- •Headache and bilateral third nerve palsy
- •Diagnosis: Pituitary apoplexy
- •Progressive sixth nerve palsy
- •What aspect of this patient’s presentation provides the most compelling diagnostic clue?
- •Diagnosis: Petrous ridge meningioma
- •Midline and bilateral abnormalities
- •Bilateral idiopathic sixth nerve palsy
- •Is a diagnosis of vasculopathic sixth nerve palsy still tenable here?
- •Diagnosis: Clivus tumor
- •Atypical pseudotumor cerebri syndrome
- •What features of this case are atypical for a diagnosis of IIH? What alternative diagnosis should be considered?
- •Diagnosis: Superior sagittal sinus thrombosis
- •Vertical diplopia
- •Diagnosis: Symmetric Graves’ disease
- •FURTHER READING
- •Neuro-imaging
- •Canalicular meningioma
- •Cerebral venous thrombosis
- •Horner syndrome and carotid dissection
- •Chronic sixth nerve palsy
- •Empty sella
- •Low cerebellar tonsils
- •Sphenoid sinus mucocele
- •Dolichoectatic basilar artery
- •FURTHER READING
- •Pseudotumor cerebri syndrome
- •Chiari malformation
- •Sphenoid sinus mucocele
- •Dolichoectatic basilar artery
- •6 Failure of pattern recognition
- •Painful ophthalmoplegia
- •Where is this patient’s lesion?
- •Diagnosis: Tolosa Hunt syndrome
- •Painful ophthalmoplegia and visual loss
- •Diagnosis: Orbital apex syndrome
- •Painless diplopia
- •Diagnosis: Oculomotor nerve palsy with aberrant regeneration
- •Diagnosis: Lateral geniculate body stroke
- •FURTHER READING
- •Painful ophthalmoplegia
- •Orbital apex syndrome
- •Third nerve misdirection
- •Lateral geniculate body
- •Painless central gray spot in a teenager
- •What is the most likely cause of this patient’s neuroretinitis, and how would you test for it?
- •Diagnosis: Neuroretinitis due to cat scratch disease
- •This patient had an additional non-ocular symptom which she did not volunteer because she didn’t think it was relevant to her eye problem, yet this symptom was an important clue to the correct diagnosis. What question should be asked?
- •Bouncing vision
- •What examination techniques can help in the detection of nystagmus when the oscillatory amplitude is particularly small?
- •Diagnosis: Downbeat nystagmus due to Chiari I malformation
- •Diagnosis: Myasthenic pseudo-INO
- •FURTHER READING
- •Neuroretinitis
- •Downbeat nystagmus
- •Diagnosis: Retinitis pigmentosa
- •Diagnosis: Bilateral occipital stroke with macular sparing
- •What simple “bedside” test could be performed to further investigate this patient’s symptom?
- •Diagnosis: Small homonymous scotoma due to occipital stroke
- •Post-cardiac bypass visual loss
- •Is there another possible explanation for this patient’s visual loss, and how would you investigate this alternative mechanism?
- •Diagnosis: Bilateral homonymous hemianopic scotomas secondary to bilateral occipital tip strokes
- •Pseudo-bitemporal defects
- •What is the next step in this patient’s evaluation?
- •Diagnosis: Tilted disc syndrome
- •Diagnosis: Dominant optic atrophy
- •Diagnosis: Rod-cone dystrophy
- •FURTHER READING
- •Tilted disc syndrome
- •Dominant optic atrophy
- •9 Neuro-ophthalmic look-alikes
- •Does his clinical course change your mind about the diagnosis?
- •Acute tonic pupil vs. pharmacologic mydriasis
- •Chronic tonic pupils vs. Argyll Robertson pupils
- •Convergence spasm vs. bilateral sixth nerve palsies
- •What metabolic abnormality can produce this clinical picture?
- •Chronic progressive external ophthalmoplegia vs. progressive supranuclear palsy
- •This combination of horizontal and vertical gaze limitation with slowed saccades could be due to either supranuclear gaze palsy or ocular myopathy. How can we distinguish these two mechanisms?
- •Orbital myositis vs. sixth nerve palsy
- •FURTHER READING
- •Optic neuritis vs. Leber’s hereditary optic neuropathy
- •Acute unilateral mydriasis
- •Light near dissociation
- •Convergence spasm
- •Wernicke’s encephalopathy
- •Progressive supranuclear palsy
- •Sixth nerve palsy vs. orbital myositis
- •10 Over-reliance on negative test results
- •Unexplained visual loss
- •Diagnosis: Pernicious anemia with normal serum B12 level
- •Twinkling after embolic stroke
- •Diagnosis: Digoxin toxicity with therapeutic levels
- •Painless ptosis and diplopia
- •Headache and third nerve palsy
- •What additional test should be obtained?
- •Diagnosis: Aneurysmal third nerve palsy
- •Truly negative neuro-imaging
- •Brainstem syndrome with negative scan
- •Can you localize this patient’s lesion?
- •Homonymous hemianopia with negative neuro-imaging
- •What disease processes would you consider here?
- •Non-dominant parietal lobe syndrome with negative neuro-imaging
- •Can you localize this patient’s problem?
- •Diagnosis: Visual variant of Alzheimer’s disease
- •Progressive third nerve palsy
- •What other investigations might be helpful?
- •Diagnosis: Third nerve palsy secondary to nasopharyngeal carcinoma
- •Upgaze palsy
- •Diagnosis: Shunt malfunction in the absence of ventriculomegaly
- •FURTHER READING
- •Digoxin toxicity
- •Myasthenia
- •Aneurysmal third nerve palsy
- •One-and-a-half syndrome
- •Cortical visual loss with negative neuro-imaging
- •Skull base tumors with negative imaging
- •Shunt failure with negative neuro-imaging
- •11 Over-ordering tests
- •Isolated unilateral mydriasis
- •If an isolated, enlarged and poorly reactive pupil is not a sign of a pCOM aneurysm, what other causes should be considered?
- •Diagnosis: Adie’s tonic pupil
- •Acute unilateral visual loss with disc edema
- •Diagnosis: Non-arteritic anterior ischemic optic neuropathy (NAION)
- •Acute isolated sixth nerve palsy
- •What is the most likely diagnosis and what evaluation would be appropriate?
- •Diagnosis: Vasculopathic cranial mononeuropathy
- •Episodic scintillating scotoma
- •Does this patient need neuro-imaging? An EEG? Other investigation?
- •Diagnosis: Migraine aura
- •Unexplained visual loss
- •What feature in this case suggests nonorganic visual loss? Is additional ancillary testing needed?
- •Diagnosis: Non-organic visual loss
- •FURTHER READING
- •Adie’s tonic pupil
- •Non-arteritic anterior ischemic optic neuropathy
- •Vasculopathic cranial mononeuropathy
- •Migraine
- •Non-organic visual loss
- •12 Management misadventures
- •Management of idiopathic intracranial hypertension
- •Evaluation and treatment of giant cell arteritis
- •Overzealous treatment of blood pressure in NAION
- •Prednisone for demyelinating optic neuritis
- •Over-reliance on pyridostigmine bromide (Mestinon) in ocular myasthenias
- •Failure to provide symptomatic treatment
- •FURTHER READING
- •Idiopathic intracranial hypertension
- •Giant cell arteritis
- •Non-arteritic anterior ischemic optic neuropathy
- •Optic neuritis
- •Ocular myasthenia
- •Nystagmus
- •Index
Index
14–3–3 protein 168, 169
abducens nerve see sixth nerve abduction deficit
acute isolated 77
bilateral, convergence spasm 144–5 incidental 53–4
painful diplopia with isolated 152–3 accommodative spasm 145–6 acetazolamide
adverse effects 192–3
episodic ataxia with nystagmus 205 idiopathic intracranial hypertension 192–3
acetylcholine receptor antibodies 160 acetylcholinesterase (AChE) inhibitors, ocular myasthenia
201–2 acromegaly 72
acute idiopathic blind spot enlargement (AIBSE) 9, 14, 16–17
acute zonal occult outer retinopathy (AZOOR) 16 adduction deficit, farmer with 113–14
Adie syndrome 181 Adie’s tonic pupil
acute, vs pharmacologic mydriasis 139–42 chronic, vs Argyll Robertson pupils 142–4 clinical features 181
isolated unilateral mydriasis 180–1 pathophysiology 180 symptomatic treatment 205
adrenergic denervation supersensitivity 66 Alexander’s law 110–11
Alzheimer’s disease 169–72
spatial organization deficits 169, 171 visual variant 169–72
vs Creutzfeldt–Jakob disease 168, 171
207
208 Index
amaurosis fugax 23–4 amitriptyline 192 Amsler grid testing 2, 125
sudden difficulty reading the paper 123, 132 anemia, pernicious 157–8
aneurysms
acute 3rd nerve palsy 163–5 chronic 6th nerve palsy 186
fusiform, basilar artery see basilar artery, dolichoectasia posterior communicating artery see posterior
communicating artery (pCOM) aneurysms angiography
computed tomography (CTA) 72, 164–5 conventional catheter see catheter angiography magnetic resonance see magnetic resonance
angiography
see also computed tomography (CT), venography angiopathy, peripapillary microvascular 138 angiotensin converting enzyme (ACE), serum 155 angle recession, post-traumatic 10
anisocoria
acute painful ophthalmoplegia 91 angle closure glaucoma 12 Horner syndrome 66, 68, 70
anterior choroidal artery occlusion 98, 100 anterior ischemic optic neuropathy (AION) 17–18
arteritic 195–6
arteritic vs non-arteritic 195–6 bilateral sequential 195
non-arteritic see non-arteritic anterior ischemic optic neuropathy
anticardiolipin antibody syndrome 64 antihypertensive therapy
malignant hypertension 4, 8 overzealous, in NAION 197–9
antineutrophilic cytoplasmic antibodies (ANCA) 155 antiparietal cell antibodies 157
antirecoverin antibodies 22 apraclonidine
testing, Horner syndrome 66, 68 therapy 205
apraxia, constructional 169 aqueductal stenosis 45, 175
Argyll Robertson pupils, vs chronic tonic pupils 142–4 aspergillosis 88
ataxia
episodic, with nystagmus 205 optic 170
atherosclerosis 183
atrial fibrillation 158
aura, migraine 15–16, 186–8
B-cell lymphoma 77 baclofen 205
Balint’s syndrome 170 bariatric surgery 147–8, 193
basilar artery, dolichoectasia (fusiform aneurysm) 88–90
bevacizumab 198
Bielschowski three-step test 55–6 bitemporal visual field defects 118, 128
assessing vertical alignment 130 pseudo- (ocular disorders) 119, 128–35
blind spot
acute idiopathic enlargement (AIBSE) 9, 14, 16–17
enlarged, in MEWDS 11, 17 blood pressure
lowering therapy 4, 8 measurement 4, 7–8
overzealous treatment in NAION 197–9 see also hypertension
blurring of vision 1 episodic monocular 23–4 headache and 4
painful mydriasis with 10–13 see also visual loss
botulinum toxin injections 205 bouncing vision 110–13
bovine spongiform encephalopathy 168 “boxer” ptosis 70–2
brain tumor, suspected 4 brainstem
stroke, vs Wernicke’s encephalopathy 146–9 syndrome, with negative scan 165–7
breast cancer metastases, orbital apex syndrome 95 brimonidine 198
bruit 108
C-reactive protein (CRP) 195 cancer-associated retinopathy (CAR) 16, 22–3 carbamazepine 205
cardiac glycosides, toxicity 158–60
carotid arteriography see catheter angiography carotid artery
dissection 70–2 paraganglioma displacing 67–8 see also internal carotid artery
Index 209
carotid artery disease
non-arteritic anterior ischemic optic neuropathy 183–4
ocular ischemia 24 carotid-cavernous sinus fistula 107–10
direct or high flow 107 dural (low flow) 107–10 white eyed shunt 108
cat scratch disease, neuroretinitis 104–7 cataract 2–4
catheter angiography carotid-cavernous sinus fistula 109–10 cerebral aneurysm 163–5
cavernous sinus
sinusitis spreading to 88 thrombosis 109–10 tumors 94, 96–7
cavernous sinus/superior orbital fissure (spheno-cavernous) syndrome 91, 94
etiologies 93 imaging 91–4
plus ipsilateral visual loss and variable proptosis 95
ceco-central scotomas see under scotomas central gray spot, painless, in a teenager 103–7 central retinal artery occlusion (CRAO) 11, 18–19
hyperacute 18–19 metastatic breast cancer 95
central retinal vein occlusion, carotid-cavernous sinus fistula 109
cerebellar degeneration, downbeat nystagmus 111 cerebellar tonsils
descent, idiopathic intracranial hypertension 86 low 86–7
cerebral edema, hypertensive encephalopathy 6–7 cerebral polyopia 3–4
cerebral venous sinus thrombosis (CVT) 63–6, 81 clinical features 64–5, 81
laboratory evaluation 80 radiographic imaging 64–6, 82
cherry red spot, macular 11, 18–19 chest imaging, Horner syndrome 69 Chiari malformation 45, 111–12
downbeat nystagmus 111 Chiari I malformation 112–13
comitant esotropia 87 downbeat nystagmus 111, 113 oscillopsia 111
symptomatic 112–13
Chiari II malformation 173–4, 176
cholinergic denervation supersensitivity 140–1, 180–1 chorioretinal spots, small yellow-white 105
chronic progressive external ophthalmoplegia (CPEO) 151–2
vs progressive supranuclear palsy 149–52 circumpapillary telangiectatic microangiopathy 138 clinical findings, subtle 103–14
clivus tumors/lesions 77–80 clonazepam 205
cluster headache 70 cobalamin see vitamin B-12
cocaine testing, Horner syndrome 68 Cogan’s lid twitch sign 34
color vision abnormalities digitalis toxicity 159–60 dominant optic atrophy 132–3
progressive optic neuropathy 60–1 vitamin B-12 deficiency 156
computed tomography (CT) angiography (CTA) 72, 164–5 bilateral occipital stroke 122, 131, 135 bilateral occipital tip strokes 127 carotid-cavernous sinus fistula 108–9
cerebral venous sinus thrombosis 63, 65 increased intracranial pressure 65–6 neck 69
orbital apex syndrome 95 orbits 33
pituitary apoplexy 72–5 skull base 77–9 venography (CTV) 63–6
congenital anomalies 45–57 conjugate gaze palsies
one-and-a-half syndrome 165 progressive supranuclear palsy 149 Wernicke’s encephalopathy 147–8
conjunctival injection
angle closure glaucoma 12–13, 22 chronic 107–10
orbital disease 27–8 orbital myositis 152–3 thyroid eye disease 81
conjunctival vessels, dilated and tortuous 107–9 constricted fields after herniation 120–22 constructional apraxia 169
convergence spasm examination technique 144–6
vs bilateral 6th nerve palsies 144–6
210 Index
corkscrew vessels 108–9 cornea
decompensation, transient monocular visual loss 23–4
edema, angle closure glaucoma 12–13 surface drying 3
corneal dystrophy, Fuchs 23
coronary artery bypass surgery, visual loss after 125–8 corticosteroids
demyelinating optic neuritis 199–200 giant cell arteritis 195, 197
ocular myasthenia 201–3 optic perineuritis 40 orbital myositis 38–40 pituitary apoplexy 74–5 tapering 197
Tolosa Hunt syndrome 92, 94
see also methylprednisolone; prednisone cotton-wool spots
giant cell arteritis 196 malignant hypertension 4–6, 8 retinal artery occlusion 13, 18
cough headache 112 cranial nerve palsy
carotid-cavernous sinus fistula 108 vasculopathic 184–6
see also specific palsies
CRAO see central retinal artery occlusion Creutzfeldt–Jakob disease (CJD) 168–9
familial 168
Heidenhain variant 168–9 sporadic 168–9
variant (vCJD) 168
vs Alzheimer’s disease 168, 171 crossed brainstem syndromes 91 crossed cylinder testing 189
CT see computed tomography cup/disc (C/D) ratio
giant cell arteritis 196 glaucoma 8–10, 20
De Morsier’s syndrome 51 demyelinating disease
acute one-and-a-half syndrome 165–7 symptomatic treatment 203–5
see also multiple sclerosis; optic neuritis, demyelinating
denervation
Adie’s tonic pupil 140–2, 180
supersensitivity see adrenergic denervation supersensitivity; cholinergic denervation supersensitivity
developmental delay 51–3
Devic’s disease (neuromyelitis optica) 191 dexamethasone, giant cell arteritis 197 diabetes mellitus
fungal sinusitis 88
offspring of mothers with 51, 53 diethylstilbestrol 17–18
digoxin (digitalis) toxicity 158–60 diplopia
acute, in pregnancy 146–7 acute isolated horizontal 76–7
acute painless, brainstem syndrome 165–6 acute unilateral painful ophthalmoplegia 91 atypical pseudotumor cerebri syndrome 80 intermittent horizontal
chronic pink eye 107 empty sella 85
low cerebellar tonsils 86–7 monocular 2–4
painful, with isolated abduction deficit 152–3 painless horizontal
dolichoectatic basilar artery 88–9
oculomotor nerve palsy with aberrant regeneration 96–8
progressive horizontal, sphenoid sinus mucocele 87 progressive supranuclear palsy 151
and ptosis painful 37–40
painless 160–1, 200–1 slowly progressive 75–6 symptomatic treatment 203–5 vertical
causes 55 intermittent 54–7
mild radiographic changes 81–3 painless 32–4
dolichoectatic basilar artery 88–90
Doll’s head maneuver, progressive supranuclear palsy 150–1
Dorello’s canal 75–6
dorsal midbrain (Parinaud’s) syndrome 143, 173–4, 177
dot/blot hemorrhages 6–7 double-ring (halo) sign 51–2 Drance hemorrhage 10, 20 driving, diplopia during 75–6
drusen, optic disc 46–50 buried 45–50
confirming diagnosis 46–7, 49–50 dry eyes 3
Duane’s syndrome subtypes 54 type I 53–4
dural carotid-cavernous sinus fistula 107–10 dysmetria 112
Edinger–Westphal nucleus 143–4 edrophonium chloride test see Tensilon test
electroencephalography (EEG), Creutzfeldt-Jakob disease 169
electromyography (EMG), single fiber 160 electrophysiologic tests, hypovitaminosis A 21 electroretinography (ERG) 14
acute idiopathic blind spot enlargement 9, 14 cancer-associated retinopathy 22–3 hypovitaminosis A 16, 19–21
retinitis pigmentosa 118, 120 rod-cone dystrophy 125, 134 elevation deficit, incidental 27–32
Elschnig spots 6
embolic stroke, twinkling after 158–60 embolism
ocular circulation 183 retinal 23–4, 70–2
empty delta sign 65
empty sella (syndrome) 85–6 primary 86
secondary 86 enophthalmos 27 episcleral vessels
corkscrew appearance 108–9 dilation and tortuosity 107–9
episodic scintillating scotoma 186–8 erythrocyte sedimentation rate (ESR) 195 esotropia
comitant, low cerebellar tonsils 86–7 convergence spasm 144–6 dolichoectatic basilar artery 88–9 sixth nerve palsy 146
symptomatic treatment 203–5 Wernicke’s encephalopathy 148
essential thrombocytosis 81 exercise, Chiari I malformation 112 extra-ocular muscle enlargement
carotid-cavernous sinus fistula 107–9
Index 211
orbital myositis 38–9, 152 thyroid eye disease 33, 81, 83
extra-ocular muscle surgery 203–4 eye pain
acute unilateral ophthalmoplegia with 91–4 angle closure glaucoma 12
optic neuritis without 137–8 optic neuropathy 40–3 orbital disease 27
postganglionic Horner syndrome 70 ptosis and diplopia with 37–40
transient monocular visual loss (TMVL) with 24 see also headache; pain
eyelids
crease position 34–5 drooping see ptosis normal position 27–8 retraction see lid retraction
facial asymmetry 57, 85
failure to provide symptomatic treatment 203–5 false negative test results 155–77
family album tomography (FAT scan) 57 farmer with adduction deficit 113–14 fatal familial insomnia 168 fibromuscular dysplasia 70–1
flame hemorrhages 6, 8 fluorescein angiography 14
hypovitaminosis A 21 optic disc drusen 50
fogging examination techniques, non-organic visual loss 189
food-cobalamin malabsorption syndrome 157 foramen ovale, patent 123
fourth nerve palsy 3-step test 55–6 causes 55 congenital 54–7 decompensated 57
ipsilateral, and contralateral Horner syndrome 91 Fuchs corneal dystrophy 23
fundus photography, optic disc drusen 47, 50 fungal sinusitis 88
furosemide 192–3
fusional amplitudes, vertical 55, 57
fusional capacity, congenital 4th nerve palsy 55–7
gait disorder, progressive supranuclear palsy 150–1 gastric bypass surgery/gastroplasty 19, 21, 193
212 Index
Gerstmann–Straussler–Scheinker disease 168 “ghost” images 3
giant cell arteritis (GCA)
anterior ischemic optic neuropathy 195–6 evaluation and treatment 194–7
negative temporal artery biopsies 155, 195 ocular ischemia 24
glaucoma
acute angle closure 12–13, 22 optic disc changes 8–10, 20 optic neuropathy 8–10, 18, 19
globe position 27–8 Goldmann perimetry 14
abnormal field and night blindness 118 abnormal field and photopsias 124, 134 abnormal fields and temporal disc pallor 123,
133
central fields 127
constricted field after herniation 121, 129 incidental field defect 119, 130 post-cardiac bypass visual loss 127, 134 retinitis pigmentosa 117, 127
gonioscopy 2, 10 Graves’ disease
euthyroid 33–34
orbitopathy see thyroid eye disease
gray spot, painless central, in a teenager 103–7 growth failure 51–3
halo (double-ring) sign 51–2 halos around lights 10–13 hard exudates 4, 6, 8
see also macular star head tilt
longstanding pre-existing 55, 57 test (3-step test) 55–6
headache
acute angle closure glaucoma 12–13 atypical pseudotumor cerebri syndrome 80 bilateral disc edema with 5, 8
bilateral third nerve palsy and 72–5 Chiari I malformation 112
cluster 70 cough 112
disc elevation with 45–50 increased intracranial pressure 4 low cerebellar tonsils and 86–7 migraine visual aura without 187 migrainous 187
papilledema and 63–6
recurrent, with upgaze deficit 27, 29, 30 third nerve palsy and 162–5
see also eye pain; pain
hematologic malignancies, fungal sinusitis 88 hemeralopia (degradation of vision in light) 1, 21–3 hemodialysis, fungal sinusitis 88
Holmes–Adie syndrome 181 homocysteine, serum 157 homonymous hemianopia
bilateral 127–8, 134
with negative neuroimaging 168–71 small right central 123–5, 132, 133
Horner syndrome 67–9 central 68
etiologies 68
ipsilateral, and contralateral 4th nerve palsy 91 neck imaging 67–9
pharmacologic testing 66, 68 postganglionic 68
acute painful 70–2 painless 66–9
preganglionic 68 ptosis 34, 67–8
symptomatic treatment 205 Tolosa Hunt syndrome 93
hummingbird sign 151 hydrocephalus
constricted fields after herniation 120, 129 dorsal midbrain syndrome 174
shunt failure 173, 175–7 hydrocortisone, pituitary apoplexy 74–75 hydroxyamphetamine test 66, 68–70 hydroxycobalamin therapy 157 hypertension
malignant 4–8
overzealous control in NAION 197–9 see also blood pressure
hypertensive encephalopathy 6–7 hypertensive retinopathy 4–6, 8 hypopituitarism 51–3 hypotension 183, 198–9 hypovitaminosis A 15, 16, 19–21
ice test, myasthenia gravis 160–1
idiopathic intracranial hypertension (IIH) (pseudotumor cerebri) 63–4
atypical 66, 80–1 empty sella 85–6
imaging investigations 65–6 management 191–4
minor radiographic abnormalities 86 secondary 64
surgical management 192–3 immunosuppressed patients, fungal sinusitis 88
immunosuppressive therapy, ocular myasthenia 203 incidental findings 85–90
inferior ophthalmic vein, shunting of blood through 108
inferior rectus muscle entrapment, orbital floor fracture with 29–32
internal carotid artery (ICA) aneurysm 186
dissection 70–2
see also carotid artery internuclear ophthalmoplegia (INO)
myasthenia simulating 113–14 one-and-a-half syndrome 165–6 saccadic velocity 114
intra-saccadic fatigue 114
intracranial hypertension, idiopathic (IIH) see idiopathic intracranial hypertension
intracranial pressure (ICP), increased cerebral venous sinus thrombosis 63–5 imaging investigations 65–6
neck imaging 69
vs malignant hypertension 4, 7 intraocular pressure (IOP), raised angle closure glaucoma 12–13
carotid-cavernous sinus fistula 107 glaucomatous optic neuropathy 10
iris sphincter damage 180
postganglionic parasympathetic denervation 140–2
sectoral palsy 140–2
ischemic optic neuropathy 17–18
anterior see anterior ischemic optic neuropathy posterior (PION) 17–18, 127
jaw claudication 194
kuru 168
lateral choroidal artery occlusion 98–9 lateral geniculate body (LGB)
anatomy 98–9 stroke 98–100
Index 213
Leber’s hereditary optic neuropathy (LHON) vs idiopathic optic neuritis 137–9
Wallace mutation 137 levator palpebrae superioris
dehiscence of aponeurosis 34–7 fatigability testing 34
function, measurement 35 lid retraction 27
on adduction 96–8 on downgaze 97–8
thyroid eye disease 28, 81
light, degradation of vision in see hemeralopia light-near dissociation (LND)
Adie’s pupil 181 bilateral 142–4
causes and mechanisms 143 monocular 140–1
light reflex, pupillary 143–4
liver disease, vitamin A deficiency 21 look-alike diagnoses 137–53
lumbar puncture, serial 193–4
lumbo-peritoneal shunting, idiopathic intracranial hypertension 193
lung carcinoma apical 69 small cell 22
lymphoma, B-cell 77
macro square wave jerks 151 macrocytosis 156–7 macropsia 1
macular disorders diagnostic tests 2 malignant hypertension 6 neuroretinitis 104
occult 14
macular edema, malignant hypertension 4, 6
macular star
differential diagnosis 106 malignant hypertension 6 neuroretinitis 104–7
mad cow disease (bovine spongiform encephalopathy) 168 magnetic resonance angiography (MRA)
carotid-cavernous sinus fistula 109 cerebral aneurysms 163–5
internal carotid artery dissection 70–2 vertebrobasilar dolichoectasia 90
magnetic resonance imaging (MRI)
214 Index
acute painful unilateral ophthalmoplegia 91, 92 atypical pseudotumor cerebri syndrome 80–2 bilateral idiopathic 6th nerve palsy 77 carotid-cavernous sinus fistula 108–9
cavernous sinus/superior orbital fissure syndrome 91–4
cerebral venous sinus thrombosis 63–5, 81–2 Chiari I malformation 111
clivus lesions 77–80 contrast-enhanced
increased intracranial pressure 65–6 optic nerve sheath meningiomas 60–3 sphenoid wing meningioma 63
Creutzfeldt-Jakob disease 169 demyelinating disease 165–7 demyelinating optic neuritis 199 dolichoectatic basilar artery 88–9 empty sella 85
head and neck 69
idiopathic intracranial hypertension 86 increased intracranial pressure 65–6, 86 internal carotid artery dissection 70–2 low cerebellar tonsils 86–7
multiple sclerosis 203, 204 neck 67–8
optic perineuritis 40, 42 orbital disease 33, 38 orbital myositis 152–3
petrous ridge meningioma 75–76, 78 pituitary apoplexy 72, 74
postganglionic Horner syndrome 66–9, 71 progressive supranuclear palsy 151 right-sided visual field loss 98–9
shunt malfunction 173–6 skull base 77–9
sphenoid sinus mucocele 87 thyroid eye disease 81, 83 Tolosa Hunt syndrome 91–4
twinkling after embolic stroke 158, 159 Wernicke’s encephalopathy 148–9
magnetic resonance venography (MRV) 65–6 malabsorption 21
malignant hypertension 4–8 management 191–205
medial longitudinal fasciculus (MLF) 147, 165, 166
meningiomas
optic nerve sheath 61–3 petrous ridge 75–6
sphenoid wing 63 mental status changes
hypertensive encephalopathy 6 Wernicke’s encephalopathy 148
Mestinon see pyridostigmine metamorphopsia 1
metastatic disease, orbital apex syndrome 95 methylmalonic acid, serum 157 methylprednisolone
demyelinating optic neuritis 199–200 giant cell arteritis 197
multiple sclerosis 203
MEWDS (multiple evanescent white dot syndrome) 11, 17 microangiopathy, circumpapillary telangiectatic 138 micropsia 1
middle cerebral artery stroke 186 migraine 186–8
acephalgic (equivalent) 187 ancillary testing 186–8 aura 15–16, 186–8 complicated 168
vs acute idiopathic blind spot enlargement 17 miosis
during esotropia, convergence spasm 144–5 and ptosis, idiopathic 66–9
monocular visual loss
acute, with disc edema 181–4 chronic 8
large central scotoma 103–7 painful ophthalmoplegia and 94–6
progressive, painful optic neuropathy 40–1 sudden, with normal fundus 11, 17–19 transient see transient monocular visual loss
MRA see magnetic resonance angiography MRI see magnetic resonance imaging mucocele, sphenoid sinus 87–8 mucormycosis 88
Muller’s¨ muscle 35
multiple evanescent white dot syndrome (MEWDS) 11, 17
multiple sclerosis
optic perineuritis and 43 symptomatic treatment 203–5
see also demyelinating disease; optic neuritis, demyelinating
myasthenia gravis diagnostic testing 160–1 fatigable ptosis 34 ocular (OMG) 201–3
Index 215
over-reliance on pyridostigmine (Mestinon) 200–3
pseudo-internuclear ophthalmoplegia (INO) 113–14
saccadic velocity 31, 113–14 mydriasis
isolated unilateral 179–81 painful 10–13
pharmacologic, vs acute tonic pupil 139–42, 180 symptomatic treatment 205
myeloma, multiple 79 myopia, pseudo- 145–6
NAION see non-arteritic anterior ischemic optic neuropathy
nasopharyngeal biopsy 94, 172–3 nasopharyngeal carcinoma 172–3 near reflex 145
pupillary 143–4 spasm of 144–6
neck extension, Chiari I malformation 112 neck imaging
Horner syndrome 67–9
increased intracranial pressure 69 neck trauma, carotid artery dissection 70 neglect, left-sided 169
nerve stimulation studies 160 neuroimaging see radiography neuromyelitis optica 191 neuromyotonia, ocular 205 neuroretinitis 104–7
cat scratch disease 104–7 etiologies 104–5 idiopathic recurrent 106
vs malignant hypertension 6 neurosyphilis 142–3
night blindness (nyctalopia) abnormal field and 117–20, 126
photopsias and field defects 124, 134–5 slowly progressive 15, 19–21
non-arteritic anterior ischemic optic neuropathy (NAION) 181–4
overzealous treatment of blood pressure 197–9
progressive 198–9 vs arteritic 195–6
nutritional deficiency 157 nyctalopia see night blindness nystagmus 110
Chiari I malformation 112 downbeat 111
causes 111–12
Chiari I malformation 111, 113 symptomatic treatment 205
gaze-dependent 110–11
low oscillatory amplitude 110–11 periodic alternating 111, 205 rebound 111 retraction-convergence 174 symptomatic treatment 205 upbeat
causes 148
Wernicke’s encephalopathy 147, 148
obesity
bariatric surgery 147–8, 193
idiopathic intracranial hypertension (IIH) 64, 191
see also weight reduction obstructive sleep apnea syndrome 198 occipital lobes 127
occipital seizures 16 occipital stroke
bilateral, with macular sparing 122, 131 shunt malfunction 175, 176
twinkling after embolic 158–60 occipital tip stroke
bilateral 127–8, 135 unilateral 123–5
ocular disease 1–13 ocular flutter 112
ocular ischemic syndrome (OIS) 24 ocular media, disorders of
monocular diplopia 3 pinhole test 2–3
vs neurologic disease 1 ocular motility disorders
carotid-cavernous sinus fistula 108 Chiari I malformation 112–13 incidental elevation deficit 27–32 painless vertical diplopia 32–4 saccadic velocity 30, 32
see also ophthalmoplegia; specific disorders oculomotor nerve see third nerve oculosympathetic palsy see Horner syndrome one-and-a-half syndrome 165–7
ophthalmic artery embolism 183 ophthalmoplegia
216 Index
acute unilateral painful 91–4
chronic progressive external see chronic progressive external ophthalmoplegia
internuclear see internuclear ophthalmoplegia and ipsilateral optic neuropathy 94–6
painful, and visual loss 94–6 progressive supranuclear palsy 149–51 see also ocular motility disorders
optic ataxia 170
optic atrophy, dominant (Kjer’s) 133 optic chiasm lesions
visual field defects 117–18, 128, 134 vs pseudo-bitemporal defects 128–35
optic cup
size, pseudopapilledema 49
see also cup/disc (C/D) ratio; optic disc cupping optic disc
at-risk 183
drusen see drusen, optic disc elevation, and headaches 45–50 glaucomatous changes 8–10, 20 hemorrhages, pseudopapilledema 49 hypoplasia see optic nerve hypoplasia
Leber’s hereditary optic neuropathy 137–9 lesions, visual field defects 117 opacification of nerve fiber layer 47–8 sharpness of margins 48
tilted 121, 130
optic disc cupping (excavation) 10 differential diagnosis 10, 20 glaucoma 8–10, 19, 20
see also cup/disc (C/D) ratio optic disc edema
acute unilateral visual loss with 181–4 elevated intracranial pressure see papilledema headache and bilateral 8
large monocular central scotoma 103 malignant hypertension 6 neuroretinitis 105–6
painful optic neuropathy 40 pallid, giant cell arteritis 194, 196 pseudo- 138–9
retinal abnormalities with bilateral 4–5 optic disc pallor
abnormal fields and temporal 122, 132–3 progressive optic neuropathy 60–1
optic nerve hypoplasia 51–3 associated abnormalities 51–3 double-ring (halo) sign 51–2
partial 50–3 risk factors 53
superior segmental 52–3
optic nerve sheath fenestration (ONSF) idiopathic intracranial hypertension 192–3 NAION 198–9
optic nerve sheath meningiomas 61–3 optic neuritis
“chronic” 59–60 demyelinating (idiopathic) 199
prednisone therapy 199–200
vs acute idiopathic blind spot enlargement 17
vs Leber’s hereditary optic neuropathy 137–9 vs neuroretinitis 103–4, 106–7
vs optic nerve sheath meningioma 61–2 vs optic perineuritis 40–3
time course 59–60
Optic Neuritis Treatment Trial (ONTT) 199–200 optic neuropathy
acute monocular 137, 139 chronic glaucomatous 8–10, 18, 19 compressive 61–3
diagnostic tests 2
and ipsilateral ophthalmoplegia 94–6 ischemic see ischemic optic neuropathy Leber’s hereditary see Leber’s hereditary optic
neuropathy painful 40–3
progressive unilateral 59–63 time course 59–60
visual field defects 117 visual symptoms 1
optic neurotomy, radial 198 optic perineuritis (OPN) 40–3
vs optic neuritis 41–3
optical coherence tomography (OCT) 14 orbicularis oculi, myasthenic weakness 34 orbital apex syndrome 95–6
orbital disease 27–43 radiographic diagnosis 33 restrictive 27–34
orbital floor fracture, with muscle entrapment 29–32 orbital inflammatory disease
etiologies 40
idiopathic (orbital pseudotumor) 38–41 paranasal sinusitis and 88 presumptive diagnosis 163
orbital myositis
conjunctival injection 28 idiopathic 38–40
vs 6th nerve palsy 152–3 vs Graves’ orbitopathy 39
orbital venous congestion 107–9 oscillopsia 110–13
otolaryngology (ENT) evaluation 172–3
pain
chronic pink eye 107–8
on eye movement 27, 38–40, 152 orbital inflammatory disease 38–40 postganglionic Horner syndrome 70 see also eye pain; headache
painful mydriasis 10–13 panhypopituitarism 51–3 papilledema
atypical pseudotumor cerebri syndrome 80 headache and 63–6
idiopathic intracranial hypertension 86, 191–2, 194
shunt malfunction 175
vs malignant hypertension 4, 6–7, 49 vs optic disc drusen 47–50
see also optic disc edema; pseudopapilledema paragangliomas 67–9
paramedian pontine reticular formation (PPRF) 114, 147, 165–6
paranasal sinus disease 87–88 paraneoplastic syndromes
cancer-associated retinopathy (CAR) 16, 22–3 downbeat nystagmus 111
parietal lobe syndrome, non-dominant, with negative neuroimaging 169–72
Parinaud’s syndrome (dorsal midbrain syndrome) 143, 173–4, 177
parkinsonian syndromes, monocular diplopia 3 patent foramen ovale 123
pattern recognition 91–100 perimetry 117
Goldmann see Goldmann perimetry limitations of automated 120 retinitis pigmentosa 117, 120
see also visual field testing
periorbital swelling, Graves’ orbitopathy 81, 83 peripapillary microvascular angiopathy 138 pernicious anemia 157–8
petrous ridge meningioma 75–6 phenylephrine 205
Index 217
photographs, old family 57 photophobia 21–3, 205 photopsias
abnormal field and 124, 134–5 after embolic stroke 158–60 gradual visual loss with 21 localizing features 14–17 persistent 14, 17
preceding acute visual loss 17–18 see also scintillations, visual
photostress test 2 pilocarpine 181, 205 pinhole test 2–3 pink eye
chronic 107–10
see also conjunctival injection pituitary apoplexy 72–5 pituitary tumor
bitemporal visual field defect 118 hemorrhage into 73 longstanding 72
polyopia 3 cerebral 3–4
positron emission tomography (PET), Alzheimer’s disease 169, 171
post-cardiac bypass visual loss 125–8 posterior ciliary artery embolism 183
posterior communicating artery (pCOM) aneurysms acute third nerve palsy 163–4, 185
isolated unilateral mydriasis 180 ruptured 12
posterior ischemic optic neuropathy (PION) 17–18, 127
posterior reversible encephalopathy syndrome 7 prednisone
acute isolated painful 3rd nerve palsy 163 demyelinating optic neuritis 199–200 giant cell arteritis 195, 197
ocular myasthenia 201, 203
orbital inflammatory disease 38–40 orbital myositis 152
tapering 197
Tolosa Hunt syndrome 92 preeclampsia–eclampsia syndrome 7 pregnancy
acute diplopia 146–7 progressive visual loss 61–2
prion diseases 168–9
progressive supranuclear palsy (PSP)
218 Index
Doll’s head maneuver 150–1 |
radial optic neurotomy 198 |
magnetic resonance imaging 151 |
radiation therapy |
symptomatic treatment 205 |
6th nerve palsy after 173 |
vs chronic progressive external ophthalmoplegia (CPEO) |
metastatic breast cancer 95 |
149–52 |
optic nerve sheath meningioma 61–2 |
proptosis |
petrous ridge meningioma 75 |
absence, orbital apex syndrome 96 |
radiography 59–82 |
carotid-cavernous sinus fistula 107–8 |
incidental findings 85–90 |
detection 27–8 |
midline and bilateral abnormalities 76–82 |
pseudo-bitemporal defects 119, 128–35 |
ordering wrong scan 59–69 |
pseudo-internuclear ophthalmoplegia (INO) |
subtle findings 70–6 |
113–14 |
true negatives 165–77 |
pseudo-myopia 145–6 |
see also specific imaging modalities |
pseudopapilledema |
ragged red fibers 152 |
buried optic disc drusen 45–50 |
RAPD see relative afferent pupil defect |
vs papilledema 47–50 |
reading glasses, impaired downgaze 205 |
pseudotumor cerebri see idiopathic intracranial |
reading the paper, sudden difficulty 122–5, 131 |
hypertension |
recoverin antibodies 22 |
psychic paralysis of gaze 170 |
reinnervation stage, Adie’s pupil 181 |
ptosis |
relative afferent pupil defect (RAPD) |
acute painful ophthalmoplegia 91–2 |
large monocular central scotoma 103 |
aponeurotic 34–7 |
Leber’s hereditary optic neuropathy 137 |
“boxer” 70–2 |
neuroretinitis 104–5 |
and diplopia |
progressive optic neuropathy 60–2 |
painful 37–40 |
renal cell carcinoma 79 |
painless 160–1, 200–1 |
rest test, myasthenia gravis 160–1 |
fatigable 34–7 |
restrictive orbitopathy 27–34 |
Horner syndrome 34, 67–8 |
retinal artery occlusion 18–19 |
and miosis, idiopathic 66–9 |
branch 13, 18 |
myogenic 35–7 |
central see central retinal artery occlusion |
neurogenic 35–7 |
retinal detachment |
senile 35 |
central serous 104–5 |
pupillary light reflex 143–4 |
malignant hypertension 6 |
pupillary near reflex 143–4 |
retinal disease |
pupillary sphincter see iris sphincter |
bilateral optic disc edema with 4 |
pupils |
invisible (occult) 13–24 |
Argyll Robertson, vs chronic tonic 142–4 |
ischemic 23–4 |
dilatation lag 68, 70 |
peripapillary 9, 14, 17 |
oculomotor nerve palsy with aberrant regeneration 96–7 |
photopsias 16–17 |
|
visual symptoms 1 |
speed of responses 143 |
retinal edema, retinal artery occlusion 13, |
symptomatic treatment of disorders 205 |
18–19 |
tonic see tonic pupils |
retinal embolism 23–24, 70–2 |
unilateral non-reactive 12 |
retinal hemorrhages |
see also anisocoria; miosis; mydriasis |
increased intracranial pressure 4, 7 |
pyridostigmine (Mestinon) |
malignant hypertension 4, 6–7 |
ocular myasthenia 200–3 |
retinal vasculature |
side-effects 201–2 |
optic disc drusen 48–9 |
|
situs inversus 121, 130 |
Index 219
retinal veins
occlusion of central 109 tortuous 49, 107
retinitis pigmentosa 118–20, 127, 128 retinol see vitamin A
retinopathy
acute zonal occult outer (AZOOR) 16 cancer-associated (CAR) 16, 22–3 hypertensive 4–6, 8
rod-cone dystrophy 125, 134–5 “ruling out” process 155
saccadic velocity
internuclear ophthalmoplegia 114 myasthenia gravis 31, 113–14 ocular motility disorders 30, 32
orbital myositis vs 6th nerve palsy 152 progressive supranuclear palsy 149, 151
sarcoidosis 155 Schilling test 157 scintillations, visual
episodic 186–8 persistent 14, 17 see also photopsias
scleral depression 2 scotomas
arcuate, painful optic neuropathy 40–1 bilateral ceco-central
dominant optic atrophy 123, 132–3 optic neuropathies causing 156 vitamin B-12 deficiency 156
ceco-central monocular 137 episodic scintillating 186–8
homonymous hemianopic see homonymous hemianopia
junctional 91
large central monocular 103–7 monocular 14
orbital apex syndrome 95
right homonymous superior quadrantopic 158–9
ring 118, 127 twinkling 9, 14–17
see also visual field defects scrapie 168
sectoral sphincter palsy 140–2 sectoranopia
homonymous horizontal 98–100 quadruple 98, 100
seizures, occipital 16
sella turcica, enlarged see empty sella septo-optic dysplasia 51
shunting
idiopathic intracranial hypertension 193 see also ventriculoperitoneal shunt
simultanagnosia 170 sinus disease 87–8
situs inversus, retinal vessels 121, 130 sixth (abducens) nerve
imaging of full course 76 nucleus, lesions 165–6
sixth nerve palsy acute isolated 184–6
after radiation therapy 173 aneurysmal 186
bilateral idiopathic 76–80 causes of bilateral 77 chronic isolated 185–6 congenital 53–4
convergence spasm vs bilateral 144–6 restrictive orbitopathy simulating 30 slowly progressive 75–6
sphenoid sinus mucocele 87 vasculopathic (ischemic) 77, 184–5 vertebrobasilar dolichoectasia 88–9 vs orbital myositis 152–3
skull base imaging 77–9
tumors, with negative scans 172–3 sleep apnea, obstructive 198
sleep test, myasthenia gravis 160–1 slit ventricle syndrome 174
small vessel disease 98–9 smell, decreased sense of 85 spasm of near reflex 144–6
spatial organization deficits 169, 171 spheno-cavernous syndrome see cavernous
sinus/superior orbital fissure syndrome sphenoid sinus mucocele 87–8
sphenoid wing meningioma 63 splinter hemorrhages
on disc margin (Drance hemorrhage) 10, 20 malignant hypertension 5–6
square wave jerks, macro 151 Stargardt’s disease 14 stellate maculopathy 104 steroids see corticosteroids strabismus surgery 203–4
220 Index
stroke
chronic 6th nerve palsy and 186 downbeat nystagmus 111
internal carotid artery dissection 72 lateral geniculate body 98–100 occipital see occipital stroke occipital tip see occipital tip stroke twinkling after embolic 158–60
Wernicke’s encephalopathy vs brainstem 146–9 subarachnoid hemorrhage 110
subtle clinical findings 103–14
sudden difficulty reading the paper 122–5, 131 superior colliculus syndrome see Parinaud’s syndrome superior oblique palsy, congenital 54–7
superior ophthalmic vein dilation 107–9
shunting of blood through 108 thrombosis 110
superior orbital fissure lesions 91, 95
see also cavernous sinus/superior orbital fissure syndrome
superior sagittal sinus thrombosis 64–5, 81–2 sympathetic pathway, to eye 66–7
symptomatic treatment, failure to provide 203–5 syphilis, tertiary 142–3
tearing, excessive 3
temporal artery biopsy, false-negative 155, 195 Tensilon test 161
positive 113, 114, 160–161 reluctance to perform 160–1
tests
false negative results 155–77 over-ordering 179–89
therapeutic nihilism 191 thiamine
deficiency 147–9 trial of therapy 148
third (oculomotor) nerve, divisions 37 third (oculomotor) nerve palsy
with aberrant regeneration (oculomotor synkinesis) 96–8
acute bilateral painful 72–5 acute isolated painful
causes 162–3
with negative neuroimaging 162–5 acute painful, with mydriasis 12 aneurysmal 163–5, 185
isolated partial 31
with isolated unilateral mydriasis 180 progressive isolated painful 172–3 with pupil sparing 185
superior division 37–8 vasculopathic (ischemic) 185 vs restrictive orbitopathy 29, 31
three-step test, Bielschowski 55–6 thrombocytosis, essential 81 thrombolytic therapy 72, 74 thymectomy 203
thyroid eye disease (Graves’ orbitopathy) lid retraction 28, 81
mild radiographic changes in symmetric 81–3 monocular diplopia 3
painless vertical diplopia 32–4 restrictive orbitopathy 30–1
vs carotid-cavernous sinus fistula 109 vs orbital myositis 39
thyroid function tests 33–4 tilted disc syndrome 121, 130 tinnitus, pulsatile 107, 110
Tolosa Hunt syndrome (THS) 91–4 diagnostic criteria 92–3
magnetic resonance imaging 91–4 tonic pupils
acute, vs pharmacologic mydriasis 139–42, 180 causes 181
chronic, vs Argyll Robertson pupils 142–4 idiopathic see Adie’s tonic pupil
sectoral sphincter palsy 140–2 top-of-the-basilar syndrome 148 topiramate 192
topless disc syndrome (superior segmental hypoplasia) 53
transient ischemic attacks (TIA), photopsias 16 transient monocular visual loss (TMVL) 23–4
corneal decompensation 23–4 internal carotid artery dissection 70 retinal vascular disease 18, 23–4
transmissible mink encephalopathy 168 trauma
internal carotid artery dissection 70, 72 restrictive orbitopathy after 29–31
triamcinolone 198
trochlear nerve see fourth nerve twinkling after embolic stroke 158–60
Uhthoff’s phenomenon, vs Chiari I malformation 112 ultrasonography, optic disc drusen 46, 49–50
Index 221
uncal herniation, constricted fields after 120–2 upgaze deficit, incidental 27–32
upgaze palsy 173–7
Valsalva maneuver, headache provoked by 112 vascular risk factors 185, 198
vasculopathic cranial mononeuropathy 184–6 ventriculoperitoneal shunt
constricted visual fields 120, 129, 131 idiopathic intracranial hypertension 193 malfunction, without ventriculomegaly 173–7
vertebrobasilar dolichoectasia 88–90 vertical fusional amplitudes 55, 57
vestibulo-ocular reflex (Doll’s head maneuver), progressive supranuclear palsy 150–1
vision
blurring see blurring of vision bouncing 110–13
degradation in light see hemeralopia dimming or darkening 1
double see diplopia hazy night 19–21 missing areas 1 swirling 21–3
visual field defects 117–28
bitemporal see bitemporal visual field defects cancer-associated retinopathy 16, 21, 23 constricted fields after herniation 120–2,
129 glaucoma 8, 10, 18
incidental 119, 128–30 inferior altitudinal
anterior ischemic optic neuropathy 181, 183 partial optic nerve hypoplasia 50–3
localizing features 117 malignant hypertension 4–5 night blindness and 117–20, 126
non-organic vs organic constriction 121–2 photopsias and 124, 134–5
post-cardiac bypass 125–8 progressive optic neuropathy 60–1 pseudo-bitemporal defects 128–35 right-sided 98–100
severe constriction, causes 121–2
sudden difficulty reading the paper 122–25, 131
temporal disc pallor and 122, 132–3 “tunnel” or “gun-barrel” 121
see also scotomas visual field testing 117
abnormal fields and temporal disc pallor 132–3 central 123, 125, 127
hypovitaminosis A 15, 21
idiopathic intracranial hypertension 194 non-organic vs organic constricted fields 121–2 twinkling scotoma 9, 14
vertical alignment of temporal field 119, 130 see also perimetry
visual loss
monocular see monocular visual loss non-organic 156, 188–9
optic disc drusen 47 pituitary apoplexy 73 progressive 59–63
sequential, with “swirling clouds of smoke” 21–3 time course 59–60
transient, atypical pseudotumor cerebri syndrome 80 unexplained 156–8, 188–9
see also blurr ing of vision visual pathways, afferent 117 vitamin A (retinol) 21
deficiency 15, 16, 19–21 serum 21
vitamin B-1 see thiamine vitamin B-12
deficiency 156–8, 179 dietary intake 157 serum testing 156–8, 179 therapy 157
Wallace mutation 137 Wegener’s granulomatosis 155 weight reduction
bariatric surgery 193
idiopathic intracranial hypertension 192 see also obesity
Wernicke’s encephalopathy 147–9 risk factors 147–8
vs brainstem stroke 146–9 white-eyed blowout 29 white-eyed shunt 108
