- •Optic Nerve Disorders
- •Preface
- •Contents
- •Contributors
- •1 Optic Neuritis
- •2 Ischemic Optic Neuropathies
- •3 Papilledema
- •5 Traumatic Optic Neuropathies
- •6 Nutritional and Toxic Optic Neuropathies
- •7 Hereditary Optic Neuropathies
- •8 Congenital Disc Anomalies
- •9 Optic Disc Tumors
- •10 Optical Coherence Tomography in Optic Nerve Disorders
- •11 The Use of Multifocal Electroretinograms and Visual Evoked Potentials in Diagnosing Optic Nerve Disorders
- •Index
Index
A |
Angiotensin-converting enzyme |
Anticoagulants |
ACE. See Angiotensin-converting |
(ACE), levels of, in |
for cerebral venous sinus |
enzyme |
sarcoidosis, 116 |
thrombosis, 68–69 |
Acetazolamide, for IIH, 75, 79 |
Anterior communicating artery |
for NAION, 35 |
Acetylsalicylic acid (ASA), for |
aneurysm, 101 |
Anti-MBP. See Anti-myelin basic |
GCA, 48 |
Anterior ischemic optic |
protein |
Activated protein C (APC), |
neuropathy (AION), |
Anti-myelin basic protein (anti- |
resistance to, NAION and, |
42–49 |
MBP), optic neuritis and, |
40 |
GCA in |
7 |
Acute sphenoid sinusitis, optic |
diagnosis of, 44–46 |
Antinuclear antibody (ANA), in |
neuritis and, 5 |
incidence of, 42 |
neuromyelitis optica, |
Addison’s disease, increased ICP |
pathophysiology of, 42–44 |
15–16 |
and, 72 |
symptoms and signs of, 42 |
Antioxidants, for FA, 187–188 |
Adrenoleukodystrophy, 190–191 |
treatment of, 46–48 |
Antiphospholipid antibody |
Adults, optic neuritis in, 1 |
visual prognosis of, 48 |
syndrome, optic neuritis |
Aicardi syndrome, with congenital |
OCT for, 240 |
and, 6 |
disc pigmentation, 215 |
optic neuritis v., 3 |
Anti-phospholipid protein (anti- |
AIDS |
other etiologies of, 49 |
PLP), optic neuritis and, 7 |
cryptococcosis and, 118–119 |
Anterior visual pathway gliomas |
Anti-PLP. See Anti-phospholipid |
tuberculosis and, 117 |
benign |
protein |
AION. See Anterior ischemic |
course and prognosis of, |
APC. See Activated protein C |
optic neuropathy |
107–108 |
Apoptosis, with traumatic optic |
Alcohol use |
histopathology of, 106–107 |
neuropathy, 137 |
cavernous hemangioma and, |
incidence of, 103–104 |
Aqueductal stenosis, in |
225 |
management of, 108–109 |
papilledema, 66 |
optic neuropathy with, 154 |
neuroimaging of, 106 |
Arcuate defects |
Amblyopia, tobacco-alcohol, |
NF-I association with, 104 |
in NAION, 31 |
optic neuropathy with, 154 |
symptoms and signs of, |
in suprasellar meningioma, 98 |
Amiodarone, in optic |
104–106 |
ASA. See Acetylsalicylic acid |
neuropathy, 157–159 |
malignant |
Ascites, with benign anterior |
Amphotericin B, intravenous, for |
epidemiology of, 109 |
visual pathway gliomas, |
cryptococcosis, 118–119 |
neuroimaging of, 110 |
109 |
ANA. See Antinuclear antibody |
pathology of, 110 |
Aspirin, for NAION, 35–36 |
Anemia |
prognosis and treatment of, |
Astigmatism, optic nerve |
IIH and, 72–73 |
111 |
hypoplasia and, 201 |
increased ICP and, 72 |
symptoms and signs of, |
Astrocytic hamartoma |
NAION with, 38, 40 |
109–110 |
diagnostic testing for, 222 |
PION with, 50–51 |
Anthrax, optic neuritis with, 4 |
histopathology of, 222 |
271
272 |
|
Index |
Astrocytic hamartoma (cont.) |
Bromocriptine, for pituitary |
Cerebral autosomal dominant |
overview of, 221–222 |
adenoma, 96 |
arteriopathy with |
symptoms and signs of, |
Brucellosis, optic neuritis with, 4 |
subcortical infarcts and |
222–223 |
|
leukoencephalopathy |
treatment of, 223 |
C |
(CADASIL), NAION in, |
Atherosclerosis, NAION with, 35 |
Cabergoline, for pituitary |
41 |
ATP deficiency |
adenoma, 96 |
Cerebral venous sinus thrombosis |
in LHON, 152 |
CADASIL. See Cerebral |
clinical presentation of, 68 |
in optic neuropathy, 153 |
autosomal dominant |
IIH v., 72 |
Autoimmune disease, optic |
arteriopathy with |
in papilledema, 67–69 |
neuritis and, 5–6 |
subcortical infarcts and |
CHAMPS. See Controlled High- |
Autosomal dominant progressive |
leukoencephalopathy |
Risk Subjects Avonex |
optic atrophy with |
Calpain, optic neuritis with, 7 |
Multiple Sclerosis |
congenital deafness, 183 |
Canavan’s syndrome, 192 |
Prevention Study |
Autosomal dominant progressive |
Cantholysis, lateral, for traumatic |
Chemotherapy |
optic atrophy with |
optic neuropathy, 139 |
for benign anterior visual |
progressive deafness and |
Canthotomy, lateral, for |
pathway gliomas, 109 |
ataxia, 184 |
traumatic optic |
for meningeal metastasis, 112 |
Autosomal recessive optic |
neuropathy, 139 |
for ONSM, 91 |
atrophy, 181 |
Capillary hemangioma |
for optic disc tumor, 112–113 |
Azathioprine |
cavernous hemangioma v., 225 |
for paraneoplastic optic |
for GCA, 47 |
histopathology of, 224 |
neuropathy syndromes, 21 |
for NMO, 16–17 |
symptoms and signs of, |
for suprasellar meningioma, 99 |
for sarcoidosis, 116 |
223–224 |
Children |
|
treatment of, 224 |
IIH in, 79–80 |
B |
Carbidopa, for NAION, 36 |
neurodegenerative disorders |
Bacterial infection, optic neuritis |
Carboplatin, for benign anterior |
of, 189–192 |
and, 5 |
visual pathway gliomas, |
optic neuritis in, 1 |
Bariatric surgery |
109 |
MS risk factors with, 11–12 |
for IIH, 78–79 |
Carotid artery stenosis, NAION |
Chlamydia |
for papilledema, 72 |
with, 34 |
AION and, 44 |
BDGF. See Brain-derived growth |
Carotid-ophthalmic artery |
NAION and, 38 |
factor |
aneurysm, 102 |
Chloramphenicol, in optic |
Behçet’s disease, AION with, 49 |
Caspase inhibitors, for traumatic |
neuropathy, 159 |
Behr’s syndrome, 181–182 |
optic neuropathy, 140 |
Choroidal folds, with elevated |
BENEFIT. See Betaseron in |
Cataract surgery, traumatic optic |
ICP, 64 |
Newly Emerging MS for |
neuropathies after, 142–143 |
Choroidal melanoma |
Initial Treatment |
Cat scratch disease, optic neuritis |
diagnosis of, 229 |
Betaseron in Newly Emerging |
with, 4 |
symptoms of, 229 |
MS for Initial Treatment |
Cavernous hemangioma |
treatment of, 229 |
(BENEFIT), interferon |
diagnostic testing for, 225 |
Chronic inflammatory |
beta-1a in, 14 |
histopathology of, 225 |
demyelinating |
Blepharoplasty, traumatic optic |
symptoms and signs of, |
polyneuropathy (CIDP), |
neuropathies after, 144 |
224–225 |
papilledema and, 67 |
Blurry vision, with ocular |
treatment for, 225 |
Churg-Strauss angiitis, AION |
lymphoma, 113 |
CDMS. See Clinical definite |
with, 49 |
Bone marrow transplantation, |
multiple sclerosis |
CIDP. See Chronic inflammatory |
for MPS, 190 |
Central retinal artery occlusion |
demyelinating |
Bradykinin, with traumatic optic |
(CRAO), with optic disc |
polyneuropathy |
neuropathy, 137 |
drusen, 212 |
Clinical definite multiple |
Brain-derived growth factor |
Central retinal vein occlusion |
sclerosis (CDMS) |
(BDGF), for traumatic |
(CRVO), with optic disc |
interferon beta-1a and, 13–14 |
optic neuropathy, 141 |
drusen, 212 |
optic neuritis and, 1 |
Brimonidine, for NAION, 36 |
Central scotomas, in NAION, 31 |
risk of, 8–9 |
Index |
|
273 |
Clomiphene citrate, in optic |
Computed tomography (CT) |
optic disc dysplasia, 209 |
neuropathy, 161 |
of benign anterior visual |
papillorenal syndrome, 209 |
Coagulopathies, NAION with, |
pathway gliomas, 106 |
Congenital disc pigmentation, |
40–41 |
of cerebral venous sinus |
214–215 |
Cochrane Database Systematic |
thrombosis, 68 |
Congenitally anomalous disc |
Review, for cerebral |
of craniopharyngioma, 100 |
size |
venous sinus thrombosis, |
of fibrous dysplasia, 103 |
congenital tilted disc |
68–69 |
of Grave’s ophthalmopathy, 92 |
syndrome, 204–206 |
Coenzyme Q |
of idiopathic orbital |
homonymous hemioptic |
for FA, 187–188 |
inflammatory |
hypoplasia, 203 |
for LHON, 177 |
pseudotumor, 94 |
megalopapilla, 203 |
Color Doppler imaging |
of IIH, 70, 74 |
optic nerve hypoplasia, |
for GCA, 45 |
of malignant anterior visual |
201–203 |
for traumatic optic neuropathy, |
pathway gliomas, 110 |
segmental optic nerve |
136 |
of ocular lymphoma, 114 |
hypoplasia, 203 |
Color vision, in optic neuritis, 2 |
of ONSM, 89 |
Congenital tilted disc syndrome |
residual deficits with, 11 |
of optic disc tumor, 112 |
clinical features of, 205 |
Combined hamartoma of retina |
of papilledema, 65–66 |
overview of, 204–205 |
and retinal pigment |
of pituitary apoplexy, 97 |
symptoms of, 205–206 |
epithelium |
of sphenoid wing meningioma, |
Continuous positive airway |
diagnosis of, 230 |
99 |
pressure (CPAP), for IIH, |
histopathology of, 230 |
of traumatic optic neuropathy, |
73–74 |
treatment of, 230 |
135–136 |
Contrast sensitivity, in optic |
Complete blood cell count, for |
Congenital disc anomalies, |
neuritis, 2 |
nutritional optic |
201–215 |
residual deficits with, 11 |
neuropathies, 151 |
congenitally anomalous disc |
Controlled High-Risk Subjects |
Compressive optic neuropathies |
size, 201–206 |
Avonex Multiple Sclerosis |
of anterior visual pathway, |
congenital tilted disc |
Prevention Study |
88–91 |
syndrome, 204–206 |
(CHAMPS), interferon |
optic nerve sheath |
homonymous hemioptic |
beta-1a in, 13–14 |
meningiomas, 88–91 |
hypoplasia, 203 |
Corticosteroids |
of optic nerve, 92–95 |
megalopapilla, 203 |
for GCA, 46–47 |
Grave’s ophthalmopathy, |
optic nerve hypoplasia, |
for Grave’s ophthalmopathy, |
92–94 |
201–203 |
93 |
idiopathic orbital |
segmental optic nerve |
for IIH, 76, 79 |
inflammatory |
hypoplasia, 203 |
for NAION, 35 |
pseudotumor, 94–95 |
elevated optic disc anomalies, |
for ocular lymphoma, 114 |
sellar and suprasellar |
210–215 |
for optic neuritis, 12–13 |
compressive lesions, 95–103 |
congenital disc |
for pituitary apoplexy, 97 |
anterior communicating |
pigmentation, 214–215 |
for sarcoidosis, 116 |
artery aneurysm, 101 |
hyaloid system remnants, |
for traumatic optic neuropathy, |
carotid-ophthalmic artery |
213–214 |
138 |
aneurysm, 102 |
myelinated nerve fibers, |
CPAP. See Continuous positive |
craniopharyngioma, 99–101 |
214 |
airway pressure |
fibrous dysplasia, 102–103 |
optic disc drusen, 210–213 |
Craniopharyngioma |
internal carotid aneurysm, |
excavated optic disc anomalies, |
epidemiology of, 99–100 |
101 |
206–209 |
management of, 101 |
pituitary adenoma, 95–97 |
morning glory disc anomaly, |
neuroimaging of, 100 |
pituitary apoplexy, 97 |
206–207 |
pathology of, 100–101 |
sphenoid sinus mucocele, 102 |
optic disc coloboma, |
symptoms and signs of, 100 |
sphenoid wing meningioma, |
207–208 |
CRAO. See Central retinal artery |
99 |
optic disc pit, 208–209 |
occlusion |
suprasellar meningioma, |
peripapillary staphyloma, |
C-reactive protein (CRP), in |
97–99 |
208 |
GCA, 44–46 |
274 |
|
Index |
Crohn’s disease |
Wolfram syndrome with, |
Elevated optic disc anomalies |
AION with, 49 |
182–183 |
congenital disc pigmentation, |
increased ICP and, 74 |
Diabetes insipidus, diabetes |
214–215 |
CRP. See C-reactive protein |
mellitus, optic atrophy, |
hyaloid system remnants, |
CRVO. See Central retinal vein |
and sensorineural hearing |
213–214 |
occlusion |
loss (DIDMOAD). See |
myelinated nerve fibers, 214 |
Cryotherapy, for capillary |
Wolfram syndrome |
optic disc drusen, 210–213 |
hemangioma, 224 |
Diabetic papillopathy, as |
Elevated sedimentation rate |
Cryptococcosis |
NAION, 37 |
(ESR), in GCA, 44–46 |
diagnostic testing for, 118 |
DIDMOAD. See Diabetes |
ENA. See Extractable nuclear |
epidemiology of, 118 |
insipidus, diabetes |
antigen |
management of, 118–119 |
mellitus, optic atrophy, |
Encephalitogenic antibodies, |
pathology of, 118 |
and sensorineural hearing |
optic neuritis and, 6 |
symptoms and signs of, 118 |
loss |
Endoscopic sinus surgery, |
CT. See Computed tomography |
Digoxin, for optic neuropathy, |
traumatic optic |
Cuban epidemic, of optic |
157–159 |
neuropathies after, 144 |
neuropathy, 153 |
Diphenylhydantoin, for NAION, |
EOG. See Electro-oculogram |
Cup, absent, in NAION, 32 |
35 |
ERG. See Electroretinogram |
Cup-to-disc ratio |
Diplopia, with Grave’s |
ESR. See Elevated sedimentation |
in DOA, 178 |
ophthalmopathy, 93–94 |
rate |
in NAION, 31–34, 37 |
Direct argon laser |
Ethambutol |
in SIAION, 38 |
photocoagulation, for |
for optic neuropathy, 159 |
Cyanide, optic neuropathy from, |
capillary hemangioma, 224 |
for tuberculosis, 117–118 |
154–155 |
Disulfiram, in optic neuropathy, |
Ethylene glycol, in optic |
Cyanocobalamin |
159 |
neuropathy, 156 |
for optic neuropathy, 153 |
Dizocilpine, for traumatic optic |
Excavated optic disc anomalies |
for vitamin B12 deficiency, 153 |
neuropathy, 140 |
morning glory disc anomaly, |
Cyclophosphamide |
DOA. See Dominant optic |
206–207 |
for GCA, 47 |
atrophy |
optic disc coloboma, 207–208 |
for idiopathic orbital |
Dominant optic atrophy (DOA) |
optic disc pit, 208–209 |
inflammatory |
diagnostic testing for, 179 |
peripapillary staphyloma, 208 |
pseudotumor, 94–95 |
histopathology of, 179 |
Extractable nuclear antigen |
for sarcoidosis, 116 |
incidence of, 177 |
(ENA), in neuromyelitis |
Cyclosporin A, for GCA, 47 |
molecular genetics and genetic |
optica, 15–16 |
Cyclosporine |
heterogeneity of, 179–180 |
|
for idiopathic orbital |
NTG v., 180–181 |
F |
inflammatory |
pathophysiology of, 179 |
FA. See Friedreich’s ataxia |
pseudotumor, 94–95 |
symptoms and signs of, |
Farnsworth-Munsell 100-hue test, |
for sarcoidosis, 116 |
177–179 |
for optic neuritis, 2, 11 |
Cytomegalovirus, infiltration of |
treatment of, 180 |
Fatal X-linked optic atrophy, |
optic nerve, 119 |
Doxycycline, for increased ICP, |
ataxia, and deafness, 185 |
|
74 |
Fibrous dysplasia |
D |
Drugs, in toxic optic |
epidemiology of, 102 |
Danazol, for increased ICP, 74 |
neuropathies, 151 |
management of, 103 |
Dandy criteria, for IIH, 70, 74 |
|
neuroimaging of, 103 |
Dapsone, for GCA, 47 |
E |
pathology of, 103 |
Demyelination |
Electro-oculogram (EOG), for |
symptoms and signs of, 102 |
cell-mediated damage in, 6–7 |
congenital tilted disc |
Fluconazole, oral, for |
optic neuritis and, 6–7 |
syndrome, 205 |
cryptococcosis, 118–119 |
Dexamethasone, for tuberculosis, |
Electroretinogram (ERG). See |
Flucytosine, oral, for |
118 |
also Multifocal |
cryptococcosis, 118–119 |
Diabetes |
electroretinogram |
Fluorescein angiography |
diabetic papillopathy with, 37 |
for congenital tilted disc |
for astrocytic hamartoma, 222 |
NAION with, 34, 40 |
syndrome, 205 |
for cavernous hemangioma, 225 |
Index
for choroidal melanoma, 229 for combined hamartoma of
retina and retinal pigment epithelium, 230
for GCA, 45
for NAION, 34–35 OCT v., 242
for optic disc drusen, 210–211 for optic disc tumor, 112
for papilledema, 65
for racemose hemangioma, 227 Fluoroquinolones, for increased
ICP, 74
Folate treatment, for optic neuropathy, 154–155
Folic acid deficiency, in optic neuropathy, 155
Formate accumulation, in optic neuropathy, 153
Foster Kennedy syndrome papilledema in, 65 suprasellar meningioma in, 98
Free radicals, with traumatic optic neuropathy, 137
Friedreich’s ataxia (FA) clinical features of, 186 diagnosis of, 187 management of, 187–188
molecular genetics of, 186–187 overview of, 186 pathophysiology of, 187
Funduscopic examination of benign anterior visual
pathway gliomas, 105 of LHON, 172
of ONSM, 88–89
for optic disc drusen, 210 of sarcoidosis, 115
for suprasellar meningioma, 98 for traumatic optic neuropathy,
135
Fundus findings, in optic neuritis, 2–3
Furosemide, for IIH, 75–76
G
Ganglioglioma of optic nerve, 111
GDGF. See Glial-derived growth factor
Gene therapy
for LHON, 176–177
for traumatic optic neuropathy, 141–142
Genetic mutations of DOA, 179–180 of FA, 186–187
of LHON, 175–176
of Wolfram syndrome, 182–183 Giant cell arteritis (GCA), 42
diagnosis of, 44–46 incidence of, 42 pathophysiology of, 42–44 PION from, 50
symptoms and signs of, 42 treatment of, 46–48
visual prognosis of AION in, 48
Glial-derived growth factor (GDGF), for traumatic optic neuropathy, 141
Glial tumors, of retina, 221–223 Goldenhar’s syndrome, increased
ICP and, 74
Gorlin syndrome, with myelinated nerve fibers, 214
Granulomatous infections, in ICP and papilledema, 67
Grave’s ophthalmopathy diagnostic testing for, 92–93 epidemiology of, 92 management of, 93–94 pathology of, 93
symptoms and signs of, 92 Gray matter neurodegenerative disorders, infantile
neuroaxonal dystrophy, 190
Guillain-Barré syndrome, papilledema and, 67
H
Hamartoma. See Combined hamartoma of retina and retinal pigment epithelium
Headache
in IIH
in children, 79–80 medical treatment for, 75
in papilledema, 62
HELP. See Heparin-induced extracorporeal low-density lipoprotein/fibrinogen precipitation
Hemocysteine metabolism, NAION and, 40
Heparin, for cerebral venous sinus thrombosis, 69
275
Heparin-induced extracorporeal low-density lipoprotein/ fibrinogen precipitation (HELP), for NAION, 35–37
Hereditary ataxias FA, 186–188 SCA-1, 188
Hereditary motor and sensory neuropathy VI (HMSN6), 188–189
Hereditary optic atrophy with progressive deafness and polyneuropathy, 184–185
Hereditary optic neuropathy, 171–193
autosomal dominant progressive optic atrophy with congenital deafness, 183
autosomal dominant progressive optic atrophy with progressive deafness and ataxia, 184
autosomal recessive optic atrophy, 181
autosomal recessive optic atrophy with progressive hearing loss, spastic quadriplegia, dementia, and death, 184–185
Behr’s syndrome, 181–182 DOA, 177–180
fatal X-linked optic atrophy, ataxia, and deafness, 185 in hereditary ataxias, 186–188
hereditary optic atrophy with progressive deafness and polyneuropathy, 184–185
in hereditary polyneuropathies, 188–189
LHON, 171–177 MGA, 183
in neurodegenerative disorders of children, 189–192
NTG, 180–181 opticoacoustic nerve atrophy
with dementia, 185 other syndromes, 192 PEHO syndrome, 185–186 SLOS, 192–193
Wolfram syndrome or DIDMOAD, 182–183
X-linked optic atrophy, 181
276 |
|
Index |
Hereditary polyneuropathies |
histopathology of, 94 |
ganglioglioma of optic nerve, |
HMSN6 as, 188–189 |
management of, 94–95 |
111 |
HSAN3 as, 189 |
symptoms and signs of, 94 |
malignant anterior visual |
Hereditary sensory and |
Idiopathic perioptic neuritis |
pathway gliomas, 109–111 |
autonomic neuropathy |
diagnostic testing for, 116–117 |
secondary tumors, 111–115 |
type III (HSAN3), 189 |
epidemiology of, 116 |
leukemic infiltration, 114–115 |
Herpes zoster |
management of, 117 |
lymphomatous infiltration, |
AION with, 49 |
pathology of, 117 |
113–114 |
PION with, 50 |
symptoms and signs of, 116 |
meningeal metastasis, |
HIV |
IIH. See Increased intracranial |
111–112 |
cryptococcosis and, 118 |
hypertension |
myelomatous and other |
optic neuritis and, 4 |
IL-6. See Interleukin-6 |
lymphoreticular tumor |
HMSN6. See Hereditary motor |
IL-10. See Interleukin-10 |
infiltration, 115 |
and sensory neuropathy |
IL-12. See Interleukin-12 |
other metastases, 112–113 |
VI |
Immunosuppressive agents |
Inflammation, in traumatic optic |
Hodgkin’s disease, optic nerve |
for GCA, 47 |
neuropathy, 138 |
infiltration with, 113 |
for Grave’s ophthalmopathy, |
Infliximab |
Homonymous hemioptic |
93 |
for GCA, 47–48 |
hypoplasia, 203 |
Increased intracranial |
in optic neuropathy, 160–161 |
HSAN3. See Hereditary sensory |
hypertension (IIH) |
Interferon-alpha, in optic |
and autonomic |
cerebral venous sinus |
neuropathy, 160 |
neuropathy type III |
thrombosis v., 72 |
Interferon beta-1a |
Hyaloid system remnants, |
in children, 79–80 |
for CDMS, 13–14 |
213–214 |
diagnostic criteria for, 70 |
for NMO, 17 |
Hydroxychloroquine retinopathy, |
epidemiology/genetics of, 70 |
for optic neuritis, 13–15 |
OCT in, 243 |
management of, 74–79 |
Interleukin-6 (IL-6) |
Hydroxyurea, for ONSM, 91 |
medical treatment, 75–76 |
in GCA, 44–45 |
Hyperbaric oxygen, for NAION, |
surgical treatment, 76–79 |
with ocular lymphoma, 113 |
36 |
neuroimaging features of, 74 |
Interleukin-10 (IL-10), with |
Hypertension, NAION with, 34, |
in papilledema, 64, 66, 69–79 |
ocular lymphoma, 113 |
40 |
pathogenesis of, 71–72 |
Interleukin-12 (IL-12), with |
Hyperthyroidism, increased ICP |
during pregnancy, 79 |
ocular lymphoma, 113 |
and, 72 |
presentation and course of, |
Internal carotid aneurysm, 101 |
Hypotension |
69–70 |
International Optic Nerve |
NAION with, 35, 38 |
symptoms of, 69 |
Trauma Study, traumatic |
PION with, 50–51 |
visual course and prognosis of, |
optic neuropathy in, |
Hypothalamic invasion, by |
70–71 |
138–139 |
benign anterior visual |
Inducible nitric oxide synthase |
Intracellular calcium, with |
pathway gliomas, 105–106 |
(NOS), with traumatic |
traumatic optic |
Hypothalamus, with malignant |
optic neuropathy, 137 |
neuropathy, 137 |
anterior visual pathway |
Infantile neuroaxonal dystrophy, |
Intracranial pressure (ICP), |
gliomas, 110 |
190 |
increased |
Hypothyroidism, increased ICP |
Infiltrative optic neuropathies |
causes of, 66–67 |
and, 72 |
infectious, 117–119 |
disorders and medications |
|
cryptococcosis, 118–119 |
with, 72–73 |
I |
other etiologies, 119 |
features of, 62 |
Iatrogenic malabsorption |
tuberculosis, 117–118 |
in IIH, 71–72 |
syndrome, in optic |
inflammatory, 115–117 |
in papilledema, 62–65 |
neuropathy, 155–156 |
idiopathic perioptic neuritis, |
Intraneural growth, of benign |
ICP. See Intracranial pressure |
116–117 |
anterior visual pathway |
Idiopathic orbital inflammatory |
sarcoidosis, 115–116 |
gliomas, 107 |
pseudotumor |
primary tumors, 103–111 |
Intraocular pressure (IOP), |
diagnostic testing for, 94 |
benign anterior visual |
elevated, NAION with, |
epidemiology of, 94 |
pathway gliomas, 103–109 |
39–40 |
Index |
|
277 |
Intravenous immunoglobulin |
histopathology of, 174 |
Magnetic resonance imaging |
(IVIG) |
molecular genetics and genetic |
(MRI) |
for NMO, 17 |
heterogeneity of, 175–176 |
of benign anterior visual |
for optic neuritis, 13 |
OCT for, 242 |
pathway gliomas, 106 |
IONDT. See Ischemic Optic |
optic neuritis v., 3–4 |
of craniopharyngioma, 100 |
Neuropathy |
pathophysiology of, 174–175 |
of cryptococcosis, 118 |
Decompression Trial |
symptoms and signs of, |
of fibrous dysplasia, 103 |
IOP. See Intraocular pressure |
171–172 |
of GCA, 45–46 |
Ischemic optic neuropathies, 31–52 |
systemic associations of, |
of Grave’s ophthalmopathy, 92 |
AION, 42–49 |
173–174 |
of idiopathic orbital |
NAION, 31–42 |
visual prognosis of, 173 |
inflammatory |
PION, 49–52 |
Leukemic infiltration |
pseudotumor, 94 |
Ischemic Optic Neuropathy |
epidemiology of, 114 |
of IIH, 70, 74 |
Decompression Trial |
management of, 114–115 |
of LHON, 172, 174 |
(IONDT), NAION in, 31 |
pathology of, 114 |
of malignant anterior visual |
ONDS, 35–36 |
symptoms and signs of, 114 |
pathway gliomas, 110 |
optic disc pallor, 33 |
Levodopa, for NAION, 35–36 |
of multiple sclerosis, 8–9 |
visual acuity, 32 |
LHON. See Leber’s hereditary |
of ocular lymphoma, 114 |
Ishihara color plates, for optic |
optic neuropathy |
of ONSM, 89 |
neuritis, 2 |
Linezolid, in optic neuropathy, |
of optic disc tumor, 112 |
Isoniazid, for tuberculosis, 117–118 |
160 |
of papilledema, 66 |
IVIG, Seee Intravenous |
Lipidoses, with optic neuropathy, |
of pituitary adenoma, 95–96 |
immunoglobulin |
190 |
of pituitary apoplexy, 97 |
|
Lithium, for increased ICP, 74 |
of sarcoidosis, 116 |
J |
LP shunting. See |
of sphenoid wing meningioma, |
Juvenile optic atrophy. See |
Lumboperitoneal shunting |
99 |
Dominant optic atrophy |
Lumboperitoneal (LP) shunting |
of suprasellar meningioma, 98 |
|
complications of, 78 |
of traumatic optic neuropathy, |
K |
for IIH, 77–78 |
135–136 |
Kallidin, with traumatic optic |
ONSD v., 78 |
of tuberculosis, 117 |
neuropathy, 137 |
Lupus erythematosus |
of Wolfram syndrome, 182 |
Kidneys, papillorenal syndrome |
increased ICP and, 72 |
Magnetization transfer ratio, in |
with, 209 |
optic neuritis and, 5–6 |
NMO, 15 |
Kjer’s. See Dominant optic |
PION and, 50 |
Malidixic acid, for increased ICP, |
atrophy |
Lyme disease, optic neuritis and, |
74 |
Krabbe disease, 191–192 |
4 |
MBP. See Myelin basic protein |
Kurtzke expanded disability |
Lymphomatous infiltration |
Medulloepithelioma, 221 |
status scale score, optic |
diagnostic testing for, 113 |
Megalopapilla, 203 |
neuritis with, 6–7 |
epidemiology of, 113 |
Melanocytic tumors |
|
management of, 114 |
choroidal melanoma, 229 |
L |
neuroimaging of, 114 |
combined hamartoma, 230 |
Laser interferometry, for traumatic |
symptoms and signs of, 113 |
melanocytoma, 227–229 |
optic neuropathy, 136 |
|
Melanocytoma |
Leber’s hereditary optic |
M |
diagnosis of, 228 |
neuropathy (LHON), |
Macrophages |
histopathology of, 227 |
171–177 |
in GCA, 43, 45 |
symptoms of, 227 |
ATP deficiency in, 152 |
with traumatic optic |
treatment of, 228–229 |
diagnostic testing of, 172–173 |
neuropathy, 138 |
Memantine, for traumatic optic |
gene therapy, neuroprotection, |
Macular scans, of OCT, 240 |
neuropathy, 140 |
and other treatments for, |
Magnetic resonance angiography |
Meningeal metastasis |
176–177 |
(MRA) |
diagnostic testing for, 111–112 |
heteroplasmy and |
for GCA, 46 |
management of, 112 |
environmental factors of, |
for suprasellar meningioma, |
overview of, 111 |
176 |
98 |
symptoms and signs of, 111 |
278 |
|
Index |
Meningitis, cerebral venous sinus |
retinal and optic nerve |
retinal venous sheathing with, |
thrombosis and, 68 |
disorder diagnosis with, |
3 |
Mesalazine, for increased ICP, 74 |
250–255 |
visual loss with, 1 |
Metachromatic leukodystrophy, |
fixation errors and, |
Mycophenolate mofetil, for |
191 |
251–254 |
NMO, 17 |
Methanol, in optic neuropathy, |
functional and nonorganic |
Myelinated nerve fibers, 214 |
153, 156–157 |
causes, 254–255 |
Myelin basic protein (MBP), in |
Methazolamide, for IIH, 75 |
outer retina disease and, |
optic neuritis, 6–7 |
Methotrexate |
250–251 |
|
for GCA, 47 |
Multifocal visual evoked |
N |
for meningeal metastasis, 112 |
potential (mfVEP), |
NAION. See Nonarteritic |
for sarcoidosis, 116 |
255–266 |
anterior ischemic optic |
Methylprednisolone, intravenous |
identical responses with, 257 |
neuropathy |
for GCA, 46 |
measuring latency and |
Naloxone, for traumatic optic |
for Grave’s ophthalmopathy, |
amplitude in, 259 |
neuropathy, 138 |
93 |
need for, 266 |
NASCIS-2. See National Acute |
for NMO, 16 |
optic nerve disorder diagnosis |
Spinal cord Injury Study, |
for optic neuritis, 12–13 |
with, 260–266 |
second |
for traumatic optic neuropathy, |
field confirmation with, |
National Acute Spinal cord |
138–139 |
263–264 |
Injury Study, second |
mfERG. See Multifocal |
fixation error problems, |
(NASCIS-2), traumatic |
electroretinogram |
264–266 |
optic neuropathy in, 138 |
mfVEP. See Multifocal visual |
functional or nonorganic |
Nerve fiber layer atrophy, multiple |
evoked potential |
causes, 263 |
sclerosis with, 2–3 |
MGA. See Type III 3- |
glaucomatous damage |
Neurodegenerative disorders of |
methylglutaconic aciduria |
detection, 264 |
children |
Migraine, NAION in, 41 |
optic neuritis and multiple |
gray matter neurodegenerative |
Minocycline, for increased ICP, |
sclerosis, 261–262 |
disorders, 190 |
74 |
poor producers of, 266 |
lipidoses, 190 |
Mitoxantrone, for NMO, 17 |
for unreliable field takers, |
MPS, 189–190 |
Morning glory disc anomaly |
264 |
white matter |
optic disc coloboma v., 207 |
origins of, 259–260 |
neurodegenerative |
overview of, 206 |
overview of, 245, 255 |
disorders, 190–192 |
peripapillary staphyloma v., 208 |
presentation and analysis of, |
Neuroetinitis, optic neuritis with, |
symptoms and signs of, 206 |
256–257 |
4–5 |
MPS. See Mucopolysaccharidosis |
recording of, 255–256 |
Neurofibromatosis type I (NF-I) |
MRI. See Magnetic resonance |
topographical representation |
diagnostic criteria for, 104 |
imaging |
of, 257–258 |
management with, 108 |
MS. See Multiple sclerosis |
Multiple sclerosis (MS). See also |
optic gliomas associated with, |
Mucopolysaccharidosis (MPS) |
Clinical definite multiple |
104 |
diagnosis of, 190 |
sclerosis |
prognosis with, 107–108 |
in ICP and papilledema, 66–67 |
with LHON, 173 |
Neuroimaging |
with optic neuropathy, 189–190 |
mfVEP for, 261–262 |
of benign anterior visual |
Multifocal electroretinogram |
MRI for, 8–9 |
pathway gliomas, 106 |
(mfERG), 245–255 |
OCT for, 242 |
of craniopharyngioma, 100 |
ganglion cell damage detection |
optic disc pallor and nerve |
of fibrous dysplasia, 103 |
with, 255 |
fiber layer atrophy with, |
of IIH, 74 |
measuring latency and |
2–3 |
of malignant anterior visual |
amplitude in, 247–249 |
optic neuritis with, 1–3, 6 |
pathway gliomas, 110 |
need for, 266 |
development of, 8, 10 |
of NAION, 34 |
outer retina generation of, 250 |
genetic factors of, 7–8 |
of ocular lymphoma, 114 |
overview of, 245 |
prognosis of, 10–11 |
of ONSM, 89 |
presentation of, 247 |
risk factors for, 11–12 |
of PION, 51 |
recording of, 245–247 |
tests for, 8–10 |
of pituitary adenoma, 95–96 |
Index |
|
279 |
of pituitary apoplexy, 97 |
risk factors of, 34 |
Optical canal decompression, for |
of traumatic optic neuropathy, |
symptoms and signs of, 31–32 |
traumatic optic |
135–136 |
treatment of, 35–37 |
neuropathy, 137–139 |
of tuberculosis, 117 |
Non-Hodgkin’s lymphoma |
Optical coherence tomography |
Neuromyelitis optica (NMO) |
(NHL), optic nerve |
(OCT) |
clinical course of, 16 |
infiltration with, 113 |
concluding remarks on, 243 |
diagnosis of, 15–16 |
Norepinephrine, intravenous, for |
for LHON, 172–173 |
epidemiology of, 15 |
NAION, 35 |
for occult retinal disease, |
with optic neuritis, 15–18 |
Normal-tension glaucoma (NTG) |
242–243 |
pathophysiology of, 16 |
DOA v., 178, 180 |
for optic disc drusen, 211–212 |
treatment of, 16–18 |
overview of, 180–181 |
for optic nerve disorder |
Neuroprotection, for LHON, |
treatment of, 181 |
analysis, 240–242 |
176–177 |
NOS. See Inducible nitric oxide |
for optic atrophy, 240–242 |
Neurotrophins, in traumatic optic |
synthase |
for optic disc edema, 240 |
neuropathy, 141 |
NTG. See Normal-tension |
for optic nerve anomalies, 242 |
NF-I. See Neurofibromatosis type |
glaucoma |
for optic neuritis, 10 |
I |
Nutritional optic neuropathies, |
overview of, 235 |
NHL. See Non-Hodgkin’s |
150–164 |
techniques of, 235–240 |
lymphoma |
Cuban epidemic of, 153 |
macular scans, 240 |
NLP. See No light perception |
evaluation of, 150–152 |
optic disc analysis, 237–239 |
NMDA receptor blockers, for |
signs of, 150 |
papillomacular axis line |
traumatic optic |
symptoms of, 150 |
scan, 235–237 |
neuropathy, 140 |
types of, 151–155 |
peripapillary retinal nerve |
NMO. See Neuromyelitis optica |
Nystagmus, in benign anterior |
fiber layer scan, 235–236 |
No light perception (NLP), with |
visual pathway gliomas, |
for traumatic optic neuropathy, |
traumatic optic |
105 |
135 |
neuropathy, 139–140 |
|
Optic disc |
Nonarteritic anterior ischemic |
O |
in AION, 42 |
optic neuropathy |
Obesity |
with malignant anterior visual |
(NAION), 31–42 |
with IIH, 71 |
pathway gliomas, 110 |
AION v., 42 |
with papilledema, 72 |
in NAION, 31–32 |
course and prognosis of, 32–33 |
Occult retinal disease, OCT for, |
in Papilledema, 62 |
diagnostic tests of, 34 |
242–243 |
in PION, 49 |
differential diagnosis of, 33–34 |
OCT. See Optical coherence |
Optic disc analysis, of OCT, |
atypical features, 33 |
tomography |
237–239 |
rim pallor, 33–34 |
Ocular adnexa, in traumatic optic |
Optic disc coloboma |
incidence of, 31 |
neuropathy, 135 |
overview of, 207 |
OCT for, 240 |
Ocular motility deficits, with |
symptoms and signs of, |
with optic disc drusen, 212 |
craniopharyngioma, 100 |
207–208 |
optic neuritis v., 33–34 |
ONDS. See Optic nerve |
Optic disc drusen |
other settings of, 37–42 |
decompression surgery |
complications of, 212–213 |
chlamydia, 38 |
ONSD. See Optic nerve sheath |
diagnostic tests for, 210–212 |
chronic anemias, 40 |
fenestration |
NAION with, 37–38 |
coagulopathies, 40–41 |
ONSM. See Optic nerve sheath |
overview of, 210 |
diabetic papillopathy, 37 |
meningiomas |
symptoms and signs of, 210 |
elevated introcular pressure, |
ONTT. See Optic Neuritis |
treatment of, 213 |
39–40 |
Treatment Trial |
Optic disc dysplasia, 209 |
in migraine, 41 |
OPA1 mutations, in DOA, |
Optic disc excavation |
optic disc drusen associated |
177–180 |
in DOA, 178 |
with, 37–38 |
OPA2 mutations, in X-linked |
in NTG, 178 |
shock-induced, 38–39 |
optic atrophy, 181 |
Optic disc pallor |
sleep apnea syndrome, |
Ophthalmoplegia, in benign |
multiple sclerosis with, 2–3 |
41–42 |
anterior visual pathway |
in NAION, 33 |
pathogenesis of, 34–35 |
gliomas, 105 |
visual residual deficits with, 11 |
280 |
|
Index |
Optic disc pit |
neuroimaging features of, 89 |
autosomal dominant |
overview of, 208 |
prognosis and treatment of, |
progressive optic atrophy |
symptoms and signs of, |
90–91 |
with progressive deafness |
208–209 |
symptoms and signs of, 88–89 |
and ataxia, 184 |
Optic disc tumor, 220–231 |
Optic neuritis, 1–21 |
autosomal recessive optic |
diagnostic testing for, 112 |
clinical presentation of, 1–3 |
atrophy, 181 |
glial tumors of retina, 221–223 |
signs, 1–3 |
autosomal recessive optic |
management of, 112–113 |
symptoms, 1 |
atrophy with progressive |
melanocytic tumors, 227–230 |
diagnostic and prognostic tests |
hearing loss, spastic |
choroidal melanoma, 229 |
for, 8–10 |
quadriplegia, dementia, |
combined hamartoma, 230 |
atypical, 10 |
and death, 184–185 |
melanocytoma, 227–229 |
typical, 8–10 |
Behr’s syndrome, 181–182 |
prognosis of, 113 |
differential diagnosis of, 3–6 |
DOA, 177–180 |
of sensory retina and |
mfVEP for, 261–262 |
fatal X-linked optic atrophy, |
medullary epithelium, |
MS risk factors with, 11–12 |
ataxia, and deafness, 185 |
220–221 |
in children, 11–12 |
in hereditary ataxias, |
medulloepithelioma, 221 |
recurrent, 11 |
186–188 |
retinoblastoma, 220–221 |
NAION v., 33–34 |
hereditary optic atrophy |
symptoms and signs of, 112 |
neuromyelitis optica with, 15–18 |
with progressive deafness |
vascular tumors of retina, |
diagnosis of, 15–16 |
and polyneuropathy, |
223–227 |
epidemiology of, 15 |
184–185 |
Optic nerve |
overview of, 1 |
in hereditary |
anatomy of, 130–132 |
paraneoplastic optic |
polyneuropathies, 188–189 |
intracanalicular optic nerve, |
neuropathy syndromes, |
LHON, 171–177 |
132 |
18–21 |
MGA, 183 |
intracranial optic nerve, 132 |
pathogenesis of, 6–8 |
in neurodegenerative |
optic nerve head, 130–131 |
demyelination, 6–7 |
disorders of children, |
orbital optic nerve, 131–132 |
epidemiological factors, 8 |
189–192 |
avulsion of, 133 |
genetic factors, 7–8 |
NTG, 180–181 |
mfERG diagnosing of 2, |
treatment of, 12–15 |
opticoacoustic nerve atrophy |
250–255 |
corticosteroids, 12–13 |
with dementia, 185 |
swelling of, 133 |
interferon beta-1a, 13–15 |
other syndromes, 192 |
Optic nerve decompression |
IVIG, 13 |
PEHO syndrome, 185–186 |
surgery (ONDS), for |
plasmapheresis, 13 |
SLOS, 192–193 |
NAION, 35–36 |
visual prognosis with, 10–11 |
Wolfram syndrome or |
Optic nerve hemangioblastoma |
visual residual deficits with, 11 |
DIDMOAD, 182–183 |
overview of, 225 |
Optic Neuritis Treatment Trial |
X-linked optic atrophy, 181 |
symptoms and signs of, 225–226 |
(ONTT) |
infiltrative, 103–119 |
treatment for, 226 |
conclusions from, 13 |
infectious, 117–119 |
Optic nerve hypoplasia, 201–203 |
MRI and MS with, 8 |
inflammatory, 115–117 |
diagnosis of, 201 |
optic neuritis differentiated |
primary tumors, 103–111 |
neuroimaging of, 202–203 |
with, 2 |
secondary tumors, 111–115 |
overview of, 201 |
Optic neuropathies, 88–119 |
nutritional, 150–164 |
Optic nerve sheath fenestration |
compressive, 88–103 |
Cuban epidemic of, 153 |
(ONSD) |
of anterior visual pathway, |
evaluation of, 150–152 |
benefits of, 76–77 |
88–91 |
folic acid deficiency, 155 |
complications of, 77 |
of optic nerve, 92–95 |
iatrogenic malabsorption |
for IIH, 76–77, 79 |
sellar and suprasellar |
syndrome-related, 155–156 |
LP shunting v., 78 |
compressive lesions, 95–103 |
other epidemics of, 154–155 |
overview of, 76 |
hereditary, 171–193 |
signs of, 150 |
Optic nerve sheath meningiomas |
autosomal dominant |
symptoms of, 150 |
(ONSM) |
progressive optic atrophy |
thiamine/B1 deficiency, 155 |
epidemiology of, 88 |
with congenital deafness, |
tobacco-alcohol amblyopia, |
histopathology of, 89–90 |
183 |
154 |
Index |
|
281 |
vitamin B12 deficiency, |
management, 74–79 |
Peripapillary retinal nerve fiber |
151–153 |
neuroimaging features, 74 |
layer scan, of OCT, |
vitamin E deficiency, 155 |
pathogenesis, 71–72 |
235–236 |
zinc deficiency, 155 |
during pregnancy, 79 |
Peripapillary staphyloma, 208 |
toxic, 150–164 |
visual course and prognosis, |
Pertussis, optic neuritis with, 4 |
amiodaroneand digoxin- |
70–71 |
Phosphenes |
associated, 157–159 |
with malignant anterior visual |
in optic neuritis, 1 |
chloramphenicol-associated, |
pathway gliomas, 110 |
in papilledema, 62 |
159 |
OCT for, 240 |
Photophobia, in optic neuritis, 1 |
clomiphene citrate- |
pathology of, 66 |
Photopsias, in papilledema, 62 |
associated, 161 |
signs of, 62–65 |
Pial capillary plexus, in PION, 49 |
Cuban epidemic of, 153 |
chronic, 64–65 |
PION. See Posterior ischemic |
disulfiram-associated, 159 |
early stages, 62–63 |
optic neuropathy |
ethambutol-associated, 159 |
late stages, 63 |
Pituitary adenoma |
ethylene glycol-associated, |
symptoms of, 62 |
epidemiology of, 95 |
156 |
unilateral, 65 |
management of, 96–97 |
evaluation of, 150–152 |
visual loss mechanisms in, 66 |
neuroimaging of, 95–96 |
infliximab-associated, |
Papillitis, optic neuritis with, 2, 5, |
pathology of, 96 |
160–161 |
12 |
symptoms and signs of, 95 |
interferon-alpha-associated, |
Papillomacular axis line scan, of |
Pituitary apoplexy |
160 |
OCT, 235–237 |
epidemiology of, 97 |
linezolid-associated, 160 |
Papillorenal syndrome, 209 |
neuroimaging of, 97 |
methanol-associated, 153, |
Parainfectious optic neuritis, |
pathogenesis of, 97 |
156 |
optic neuritis v., 4 |
symptoms and signs of, 97 |
methanol-induced, 156–157 |
Paraneoplastic optic neuropathy |
treatment of, 97 |
other epidemics of, 154–155 |
syndromes |
Plasmapheresis |
radiation-induced, 162–164 |
malignancies associated with, |
for NMO, 18 |
signs of, 150 |
21 |
for optic neuritis, 13 |
sildenafiland tadalafil- |
optic neuritis with, 18–21 |
Platelet-derived growth factor |
associated, 161–162 |
steroids for, 21 |
(PDGF), in GCA, 43 |
symptoms of, 150 |
treatment outcomes for, 19–20 |
Polyarteritis nodosa |
tamoxifen-associated, 161 |
Paton’s lines, with elevated ICP, |
AION with, 49 |
tobacco-alcohol amblyopia, |
64 |
PION with, 50 |
154 |
PCNSL. See Primary central |
Posterior ischemic optic |
toluene associated, 157 |
nervous system lymphoma |
neuropathy (PION), 49–52 |
traumatic, 130–144 |
PDGF. See Platelet-derived |
incidence of, 49 |
of head injury, 130–142 |
growth factor |
pathophysiology of, 49 |
of ocular surgery, 142–144 |
PEHO syndrome. See |
perioperative, 50–52 |
Opticoacoustic nerve atrophy |
Progressive |
symptoms and signs of, 49 |
with dementia, 185 |
encephalopathy with |
in systemic disorders, 49–50 |
Oral contraceptives, for increased |
edema, hypsarrhythmia, |
treatment of, 51–52 |
ICP, 74 |
and optic atrophy |
Prednisone, oral |
Orbital emphysema, 133 |
Pelizaeus-Merzbacher disease, |
for GCA, 46–47 |
|
192 |
for Grave’s ophthalmopathy, |
P |
Perforating diathermy, for |
93 |
Papilledema, 62–80 |
capillary hemangioma, 224 |
for idiopathic orbital |
asymmetric, 65 |
Periarteritis nodosa, AION with, |
inflammatory |
cerebral venous sinus |
49 |
pseudotumor, 94 |
thrombosis in, 67–69 |
Perineural growth, of benign |
for idiopathic perioptic |
with craniopharyngioma, 100 |
anterior visual pathway |
neuritis, 117 |
diagnostic testing for, 65–66 |
gliomas, 107 |
for NMO, 16–17 |
IIH and, 64, 67, 69–79 |
Periorbital injections, traumatic |
for optic neuritis, 12–13 |
diagnostic criteria, 70 |
optic neuropathies with, |
for sarcoidosis, 116 |
epidemiology/genetics, 70 |
142 |
for tuberculosis, 118 |
282
Primary central nervous system lymphoma (PCNSL), optic nerve infiltration with, 113
Progesterone, for increased ICP, 74
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome), 185–186
Proptosis, in benign anterior visual pathway gliomas, 105
Pseudotumor cerebri pathogenesis of, 71 prognosis of, 71
Pseudoxanthoma elasticum, with optic disc drusen, 212–213 Pulsatile tinnitus, in papilledema,
62
Pupillary abnormality, in optic neuritis, 2
Pyrazinamide, for tuberculosis, 117–118
Pyridoxine, for tuberculosis, 118
Q
Quadrantic defects, in NAION, 31 Quinagolide, for pituitary
adenoma, 96
R
Racemose hemangioma diagnostic testing for, 227 overview of, 226
symptoms and signs of, 226–227 visual prognosis for, 227
Radiation therapy
for benign anterior visual pathway gliomas, 109
for craniopharyngioma, 101 low-dose, for idiopathic orbital
inflammatory pseudotumor, 94
for malignant anterior visual pathway gliomas, 111
for meningeal metastasis, 112 for ocular leukemia, 114–115 for optic disc tumor, 112–113 for optic neuropathy, 162–164 for paraneoplastic optic
neuropathy syndromes, 21 for sphenoid wing
meningioma, 99
for suprasellar meningioma, 99
Radiotherapy
for choroidal melanoma, 229 for Grave’s ophthalmopathy,
93
for ocular lymphoma, 114 for ONSM, 90
for pituitary adenoma, 96 Relapsing polychondritis, AION
with, 49
Retina, glial tumors of, 221–223 Retinal hemorrhages, with optic
disc drusen, 212
Retinal nerve fiber layer (RNFL) OCT measurement of, 10, 235 with traumatic optic
neuropathy, 135 Retinal venous sheathing, with
MS, 3 Retinitis pigmentosa
OCT in, 243
with optic disc drusen, 212 Retinoblastoma
histopathology of, 220–221 overview of, 220 symptoms and signs of, 220 treatment of, 221
Retrobulbar optic neuritis, 2 Rheumatoid arthritis, AION
with, 49
Rifampin, for tuberculosis, 117–118
Rim pallor, in NAION, 33–34 Rituximab, for NMO, 17 RNFL. See Retinal nerve fiber
layer RU-486
for ONSM, 91
for suprasellar meningioma, 99
S
Sarcoidosis
diagnostic testing for, 116 epidemiology of, 115 management of, 116 optic neuritis in, 4 pathology of, 116
symptoms and signs of, 115 SCA-1. See Spinocerebellar
ataxia type 1
Scleritis, posterior, optic neuritis with, 4
Scotomas, with lymphomatous infiltration of optic nerve, 113
Index
Segmental optic nerve hypoplasia, 203
Shock-induced anterior ischemic optic neuropathy (SIAION), 38–39
Short tau inversion recovery (STIR)
for Grave’s ophthalmopathy, 92–93
for sphenoid sinus mucocele, 102
SIAION. See Shock-induced anterior ischemic optic neuropathy
Sickle cell disease, PION in, 50 Sildenafil, in optic neuropathy,
161–162
Sleep apnea syndrome IIH and, 73–74 NAION and, 41–42
SLOS. See Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome (SLOS), 192–193
Smoking. See Tobacco use Sphenoid sinus mucocele, 102 Sphenoid wing meningioma
epidemiology of, 99 management of, 99 neuroimaging of, 99 pathology of, 99 symptoms and signs of, 99
Spinocerebellar ataxia type 1 (SCA-1), 188
Stellate ganglion blocks, for NAION, 35
Stem cell implantation, for traumatic optic neuropathy, 141–142
Steroids, for paraneoplastic optic neuropathy syndromes, 21
STIR. See Short tau inversion recovery
Strachan’s syndrome, as optic neuropathy, 154
Sulfa drugs, for increased ICP, 74 Suprasellar meningioma
course and visual prognosis of, 98
epidemiology of, 97 management of, 99 neuroimaging of, 98 pathology of, 98
symptoms and signs of, 97–98
Index |
|
283 |
Surgery |
evaluation of, 150–152 |
U |
for benign anterior visual |
OCT for, 242 |
Ultrasonography |
pathway gliomas, 108–109 |
signs of, 150 |
for cavernous hemangioma, |
for craniopharyngioma, 101 |
symptoms of, 150 |
225 |
for fibrous dysplasia, 103 |
types of, 156–164 |
of optic disc tumor, 112 |
for pituitary adenoma, 96 |
Trabeculectomy, traumatic optic |
Uthohff’s phenomenon |
for sphenoid wing |
neuropathies after, |
cause of, 11 |
meningioma, 99 |
143–144 |
with LHON, 173 |
for suprasellar meningioma, 99 |
Transvitreal optic neurotomy, for |
optic neuritis with, 10–11 |
for traumatic optic neuropathy, |
NAION, 37 |
Uveitis |
138 |
Traumatic optic neuropathies, |
posterior, optic neuritis with, |
|
130–144 |
4–5 |
T |
of head injury, 130–142 |
sarcoidosis with, 115 |
Tadalafil, in optic neuropathy, |
diagnostic tests for, |
|
161–162 |
134–136 |
V |
Takayasu’s arteritis, AION with, |
epidemiology of, 130 |
Vascular endothelial growth |
49 |
localization of direct, |
factor (VEGF), in GCA, 43 |
Tamoxifen, in optic neuropathy, |
132–133 |
Vascular tumors of retina |
161 |
localization of indirect, |
capillary hemangioma, 223–224 |
Tay-Sachs disease, 190 |
133–134 |
cavernous hemangioma, |
T cells |
management of, 138–140 |
224–225 |
in GCA, 43 |
new perspectives for, |
optic nerve hemangioblastoma, |
for traumatic optic neuropathy, |
140–142 |
225–226 |
140 |
optic nerve anatomy, |
racemose hemangioma, |
Temporal artery biopsy, for |
130–132 |
226–227 |
GCA, 45 |
pathogenesis of, 137–138 |
Vasospasm, NAION with, 35 |
Temporal lobes, with malignant |
pathology of, 136–137 |
VEGF. See Vascular endothelial |
anterior visual pathway |
visual prognosis of, 136 |
growth factor |
gliomas, 110 |
of ocular surgery, 142–144 |
Ventriculoperitoneal (VP) |
Tetracycline |
after blepharoplasty, 144 |
shunting, for IIH, 77–78 |
in IIH, 75 |
after cataract surgery, |
VEP. See Visual evoked potential |
for increased ICP, 74 |
142–143 |
Vincristine, for benign anterior |
Thiamine deficiency, in optic |
after endoscopic sinus |
visual pathway gliomas, |
neuropathy, 155 |
surgery, 144 |
109 |
Thiazide diuretics, for IIH, 79 |
with periorbital injections, |
Vision loss |
Thrombocytosis, GCA and, 44 |
142 |
in AION, 42 |
Thrombolytic agents, for NAION, |
after trabeculectomy, |
in choroidal melanoma, 229 |
35 |
143–144 |
in combined hamartoma of |
Thyroid autoantibodies, in |
after vitrectomy, 143 |
retina and retinal pigment |
neuromyelitis optica, 15–16 |
Tuberculin skin test, for |
epithelium, 230 |
Thyroid ophthalmopathy, with |
tuberculosis, 117 |
in craniopharyngioma, 100 |
Grave’s ophthalmopathy, |
Tuberculosis |
in DOA, 177–178 |
92 |
epidemiology of, 117 |
in idiopathic perioptic neuritis, |
Tobacco-alcohol amblyopia, optic |
management of, 117–118 |
116 |
neuropathy with, 154 |
neuroimaging of, 117 |
in IIH, 70–71 |
Tobacco use |
optic neuritis with, 4 |
medical treatment for, 75 |
with Grave’s ophthalmopathy, |
pathology of, 117 |
in LHON, 171 |
92 |
symptoms and signs of, 117 |
in malignant anterior visual |
NAION with, 34, 40 |
Tumor-necrosis factor-α, in GCA, |
pathway gliomas, 109 |
optic neuropathy with, 154 |
47–48 |
in melanocytoma, 228 |
Toluene, in optic neuropathy, 157 |
Type III 3-methylglutaconic |
in NTG, 181 |
Topiramate, for IIH, 75 |
aciduria (MGA), 183 |
in optic disc coloboma, 207 |
Toxic optic neuropathies, |
Typhoid fever, optic neuritis with, |
in optic neuritis, 1 |
150–164 |
4 |
in papilledema, 66 |
284 |
|
Index |
Vision loss (cont.) |
in optic neuritis, 1–2 |
Wegener’s vasculitis, AION with, |
in toxic optic neuropathy, |
in traumatic optic neuropathy, |
49 |
150–151 |
135, 143 |
Weight loss, for papilledema, |
Visual acuity |
Vitamin A |
72 |
with congenital disc |
for IIH, 75 |
West Nile virus, optic neuritis |
pigmentation, 215 |
for increased ICP, 74 |
and, 4 |
with morning glory disc |
Vitamin B12, in nutritional optic |
Whipple’s disease, optic neuritis |
anomaly, 206 |
neuropathy, 151–153 |
with, 4 |
with ONSM, 88 |
Vitamin B1 deficiency, in optic |
White matter neurodegenerative |
with optic disc pit, 209 |
neuropathy, 155 |
disorders |
with optic neuritis, 1 |
Vitamin E |
adrenoleukodystrophy, |
with peripapillary staphyloma, |
deficiency of, in optic |
190–191 |
208 |
neuropathy, 155 |
Canavan’s syndrome, 192 |
Visual evoked potential (VEP) |
for FA, 187–188 |
Krabbe disease, 191–192 |
for congenital tilted disc |
Vitrectomy |
metachromatic leukodystrophy, |
syndrome, 205 |
for combined hamartoma of |
191 |
for Krabbe disease, 191 |
retina and retinal pigment |
Pelizaeus-Merzbacher disease, |
mfVEP v., 261 |
epithelium, 230 |
192 |
for nutritional optic |
for ocular lymphoma, 114 |
Wolfram syndrome |
neuropathy, 152 |
traumatic optic neuropathies |
diagnostic testing for, 182 |
for optic disc drusen, 212 |
after, 143 |
molecular genetics and |
for optic nerve hypoplasia, 201 |
Vitritis, optic neuritis with, 2 |
genetic heterogeneity of, |
for optic neuritis, 10 |
Vogt-Koyanagi-Harada disease, |
182–183 |
residual deficits with, 11 |
optic neuritis and, 5 |
symptoms and signs of, 182 |
for sarcoidosis, 116 |
VP shunting. See |
|
for traumatic optic neuropathy, |
Ventriculoperitoneal |
X |
135 |
shunting |
X-linked optic atrophy, 181 |
Visual field loss |
|
|
in benign anterior visual |
W |
Z |
pathway gliomas, 105 |
Warfarin, oral, for cerebral venous |
Zinc deficiency, in optic |
in craniopharyngioma, 100 |
sinus thrombosis, 69 |
neuropathy, 155 |
