Menu Expand
SPEC - The Retinal Atlas, 12-Month Access, Ebook

SPEC - The Retinal Atlas, 12-Month Access, Ebook

K. Bailey Freund | David Sarraf | William F. Mieler | Lawrence A. Yannuzzi

(2016)

Additional Information

Book Details

Abstract

With more than 5,000 images and comprehensive illustrations of the entire spectrum of vitreous, retina, and macula disorders, The Retinal Atlas, 2nd Edition, is an indispensable reference for retina specialists and comprehensive ophthalmologists as well as residents and fellows in training. For this edition, an expanded author team made up of Drs. K. Bailey Freund, David Sarraf, William F. Mieler, and Lawrence A. Yannuzzi, each an expert in retinal research and imaging, provide definitive up-to-date perspectives in this rapidly advancing field. This award-winning title has been thoroughly updated with new images with multimodal illustrations, new coverage and insight into key topics, and new disorders and classifications making it the most useful and most complete atlas of its kind.

  • Provides a complete visual guide to advanced retinal imaging and diagnosis of the full spectrum of retinal diseases, including early and later stages of disease.
  • Enhances understanding by presenting comparison imaging modalities, composite layouts, high-power views, panoramic disease visuals, and selected magnified areas to hone in on key findings and disease patterns.
  • Features color coding for different imaging techniques, as well as user-friendly arrows, labels, and magnified images that point to key lesions and intricacies.
  • Covers all current retinal imaging methods including: optical coherence tomography (OCT), indocyanine green angiography, fluorescein angiography, and fundus autofluorescence.
  • Depicts and explains expanding OCT uses, including spectral domain and en face OCT, and evolving retinal imaging modalities such as ultra-wide-field fundus photography, angiography and autofluorescence.
  • Presents a select team of experts, all of whom are true international leaders in retinal imaging, and have assisted in contributing to the diverse library of common and rare case illustrations.

Table of Contents

Section Title Page Action Price
Front Cover cover
IFC_Expert Consult PIN page IFC2
The Retinal Atlas i
Copyright Page iv
Color Coding—How to use this book v
Dedication vi
Table Of Contents vii
Contributors to the First Edition viii
Preface to the Second Edition ix
Contributors to the Second Edition x
Preface to the First Edition xii
References xv
Image References xvi
1 Normal 1
Retinal Histology 2
The Fundus 4
Vitreous 4
Retina 5
Macula 5
Fluorescein Angiography (FA) 6
Indocyanine Green (ICG) 7
Fundus Autofluorescence (FAF) 7
Ultra Widefield Imaging 8
Optical Coherence Tomography (OCT) 9
Optical Coherence Tomography Angiography (OCTA) 10
Optic Nerve 12
2 Hereditary Chorioretinal Dystrophies 13
Vitreoretinopathies 17
Stickler Syndrome 17
Wagner Syndrome (Wagner Vitreoretinal Degeneration) 21
Marfan Syndrome 23
Autosomal Dominant Vitreoretinochoroidopathy 25
Snowflake Vitreoretinodegeneration 26
Idiopathic Vitreoretinal Degeneration 27
Inner Retinal Dystrophies 28
Familial Internal Limiting Membrane Dystrophy (Dominantly Inherited Müller Cell Sheen Dystrophy) 28
X-Linked Juvenile Retinoschisis 29
Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis 37
Degenerative Retinal Schisis 39
Enhanced S-Cone Syndrome (Goldmann–Favre Syndrome) 40
Retinal Vascular Dystrophies 46
Hereditary or Familial Retinal Artery Tortuosity 46
Fabry Disease 51
Familial Exudative Vitreoretinopathy 53
FEVR with Norrie’s Gene 60
Incontinentia Pigmenti 61
Norrie Disease 63
Facioscapulohumeral Muscular Dystrophy 65
Parry–Rhomberg Syndrome 69
Duchenne Muscular Dystrophy 72
Dyskeratosis Congenita 75
Cohen Syndrome 76
Macular Dystrophies 77
Stargardt Disease (Stargardt Macular Dystrophy, Fundus Flavimaculatus) 77
The Spectrum of Stargardt Disease 79
Best Vitelliform Macular Dystrophy 86
Fluorescein Angiography 88
Fundus Autofluoresence 89
Optical Coherence Tomography (OCT) 90
Choroidal Neovascularization 92
Autosomal Recessive Bestrophinopathy 94
Pattern Dystrophy of the RPE 97
Adult-Onset Vitelliform Macular Dystrophy (Adult-Onset Foveomacular Dystrophy, Pseudovitelliform Macular Degeneration) 97
Butterfly-Shaped Pattern Dystrophy 99
Myotonic Dystrophy 1 (Dystrophia Myotonica, Steinert Disease, DM1) 99
Sjögren Reticular Dystrophy (Reticular Pigmentary Retinal Dystrophy of the Posterior Pole) 101
Fundus Pulverulentus 104
Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus 105
Pattern Dystrophy and Choroidal Neovascularization 107
Malattia Leventinese (Doyne Honeycomb Retinal Dystrophy, Autosomal Dominant Radial Drusen) 108
Membranoproliferative Glomerulonephritis (Mesangiocapillary Glomerulonephritis) 110
Alport Syndrome 113
Sorsby Pseudoinflammatory Fundus Dystrophy 116
North Carolina Macular Dystrophy (Macular Dystrophy of the Retina Locus 1) 119
Benign Concentric Annular Macular Dystrophy (BCAMD) 122
Fenestrated Sheen Macular Dystrophy 125
White Dot Fovea 126
Martinique Crinkled Retinal Pigment Epitheliopathy (West Indies Crinkled Retinal Pigment Epitheliopathy) 126
Cone Dystrophies 127
Cone Dystrophy 127
Rod Monochromatism (Complete Achromatopsia) 132
Occult Macular Dystrophy 134
Cone–Rod Dystrophies 135
Jalili Syndrome 136
Retinitis Pigmentosa (Generalized Rod-Cone Dystrophies 137
Non-Syndromic Retinitis Pigmentosa 137
Female Carriers of X-Linked Retinitis Pigmentosa 142
Macular Abnormalities in Retinitis Pigmentosa 143
Hole 143
Atrophy 143
Edema 144
Ring Autofluorescence 145
Epiretinal Membrane 145
Angiomatous Proliferation in Retinitis Pigmentosa 146
Sector Retinitis Pigmentosa 147
Pigmented Paravenous Retinochoroidal Atrophy (PPRCA) 149
Preserved Para-arteriolar Retinal Pigment Epithelium in Retinitis Pigmentosa 152
Syndromic Retinitis Pigmentosa 154
Mitochondrial Disorders 154
Kearns–Sayre Syndrome 154
MELAS and MIDD Syndromes (Retinopathy due to A3243G Mutation) 155
Neurogenic Weakness Ataxia and Retinitis Pigmentosa (NARP) Syndrome 160
Myoclonic Epilepsy and Ragged Red Fiber (MERRF) Syndrome 161
Ciliopathy Disorders 161
Alström Syndrome 161
Bardet–Biedl Syndrome (Laurence–Moon–Biedl–Bardet Syndrome) 163
Senior–Loken Syndrome 166
Joubert Syndrome 168
Jeune Asphyxiating Thoracic Dystrophy 169
Usher Syndrome 169
Neurological Disorders 170
Adult Refsum Disease 170
Alagille Syndrome (Arteriohepatic Dysplasia) 171
Bassen–Kornzweig Syndrome (Abetalipoproteinemia) 172
Cockayne Syndrome 173
Hallervorden–Spatz Disease (Neurodegeneration with Brain Iron Accumulation 1 (NBIA1), Pantothenate Kinase-Associated Neurodegeneration, Juvenile-Onset PKAN Neuroaxonal Dystrophy) 174
Kjellin Syndrome (Spastic Paraplegia 15, Spastic Paraplegia 11, Spastic Paraplegia and Retinal Degeneration) 175
Spinocerebellar Ataxia (Autosomal Dominant Cerebellar Ataxia) 177
Pseudo Retinitis Pigmentosa 179
Albinism 180
Oculocutaneous Albinism 180
Ocular Albinism Type I (Nettleship–Falls-Type Albinism) 181
Albinism — Female Carrier 184
Female Carrier of X-Linked Ocular Albinism 185
Choroidal Dystrophies 186
Choroideremia 186
Choroideremia—Female Carrier 195
Gyrate Atrophy (Ornithine Aminotransferase Deficiency) 196
Late-Onset Retinal Dystrophy (LORD) 202
Central Areolar Choroidal Dystrophy (CACD) 204
Posterior Polar Central Choroidal Dystrophy 205
Posterior Polar Annular Choroidal Dystrophy 206
Posterior Polar Hemispheric Choroidal Dystrophy 209
Central and Peripheral Annular Choroidal Dystrophy 210
Crystalline Retinopathies 211
Bietti Crystalline Corneoretinal Dystrophy (BCD, Bietti Crystalline Retinopathy, Bietti Crystalline Tapetoretinal Dystrophy) 211
Primary Hyperoxaluria 215
Cystinosis 216
Sjögren–Larsson Syndrome 217
Flecked Retinal Syndromes 218
Benign Flecked Retina Syndrome (Benign Familial Flecked Retina) 218
Flecked Retina of Kandori 219
Fundus Albipunctatus 220
Oguchi Disease 223
Mizuo–Nakamura Phenomenon 225
Retinitis Punctata Albescens 226
Suggested Reading 228
Stickler Syndrome 228
Wagner Syndrome 228
Marfan Syndrome 228
Autosomal Dominant Vitreoretinochoroidopathy 228
Snowflake Vitreoretinodegeneration 228
Familial Internal Limiting Membrane Dystrophy 228
X-linked Juvenile Retinoschisis 228
Stellate Nonheriditary Idiopathic Foveomacular Retinoschisis 228
Enhanced S-Cone Syndrome (Goldmann–Favre Syndrome) 228
Hereditary or Familial Retinal Artery Tortuosity 228
Fabry Disease 228
Familial Exudative Vitreoretinopathy 228
Incontinentia Pigmenti 228
Norrie Disease 228
Facioscapulohumeral Muscular Dystrophy 228
Parry–Rhomberg Syndrome 228
Duchenne Muscular Dystrophy 228
Dyskeratosis Congenita 228
Cohen Syndrome 229
Stargardt Disease 229
Best Vitelliform Macular Dystrophy 229
Autosomal Recessive Bestrophinopathy 229
Pattern Dystrophy of the RPE 229
Adult-Onset Vitelliform Macular Dystrophy 229
Butterfly-Shaped Pattern Dystrophy 229
Myotonic Dystrophy 1 229
Sjögren Reticular Pattern Dystrophy 229
Malattia Leventinese 229
Membranoproliferative Glomerulonephritis 229
Alport Syndrome 229
Sorsby Pseudoinflammatory Fundus Dystrophy 229
North Carolina Macular Dystrophy 229
Benign Concentric Annular Macular Dystrophy 229
Fenestrated Sheen Macular Dystrophy 229
Martinique Crinkled Retinal Pigment Epitheliopathy 229
Cone Dystrophy 229
Occult Macular Dystrophy 229
Cone-Rod Dystrophies 229
Jalili Syndrome 230
Non-Syndromic Retinitis Pigmentosa 230
Pigmented Paravenous Retinochoroidal Atrophy 230
Kearns-Sayre Syndrome 230
MELAS and MIDD Syndromes 230
Neurogenic Weakness Ataxia and Retinitis Pigmentosa Syndrome 230
Alström Syndrome 230
Bardet–Biedl Syndrome 230
Senior–Loken Syndrome 230
Joubert Syndrome 230
Jeune Asphyxiating Thoracic Dystrophy 230
Usher Syndrome 230
Adult Refsum Disease 230
Alagille Syndrome 230
Bassen–Korenzweig Syndrome 230
Cockayne Syndrome 230
Hallervorden–Spatz Disease 230
Kjellin Syndrome 231
Spinocerebellar Ataxia 231
Albinism 231
Choroideremia 231
Gyrate Atrophy 231
Late-Onset Retinal Dystrophy 231
Central Areolar Choroidal Dystrophy 231
Posterior Polar Choroidal Dystrophy 231
Bietti Crystalline Corneoretinal Dystrophy 231
Primary Hyperoxaluria 231
Cystinosis 231
Sjögren–Larsson Syndrome 231
Benign Flecked Retina Syndrome 231
Flecked Retina of Kandori 231
Fundus Albipunctatus 231
Oguchi Disease 231
Retinitis Puntacta Albescens 231
3 Pediatrics 233
Congenital Abnormalities 234
Retinopathy of Prematurity 234
Stage I 234
Stage II 234
Stage III 235
Stage IV-A 235
Stage IV-B 235
Stage V 235
Plus Disease 236
Spectrum of ROP 237
ROP “Popcorn Lesions” 238
ROP and Fibrous Scarring 239
Persistent Fetal Vasculature Syndrome (Persistent Hyperplastic Primary Vitreous) 240
Chorioretinal Coloboma 243
Congenital Folds 246
Congenital Systemic Disorders 247
Phakomatoses 247
Neurofibromatosis Type I 247
Neurofibromatosis Type 2 248
Combined Hamartoma of the Retina and RPE 249
Arterial–Venous Malformations (Wyburn Mason Syndrome) 249
Congenital Retinal Macrovessel 250
von Hippel–Lindau Syndrome (VHL) 251
Retinal Cavernous Hemangioma 253
Leber Congenital Amaurosis 255
Pigmented Paravenous Chorioretinal Atrophy 260
Aicardi Syndrome 261
Inborn Errors of Metabolism 262
Neuronal Ceroid Lipofuscinoses 262
Neuronal Ceroid Lipofuscinosis 1 (CLN1, Santavuori–Haltia Disease, Hagberg–Santavuori Disease) 262
Neuronal Ceroid Lipofuscinosis 2 (CLN2, Jansky–Bielschowsky Disease) 263
Neuronal Ceroid Lipofuscinosis 3 (CLN3, Batten Disease, Vogt–Spielmeyer Disease, Spielmeyer–Sjögren Disease) 263
Mucopolysaccharidoses 264
Mucopolysaccharidosis Type I (Hurler, Scheie, and Hurler–Scheie Syndrome; MPS IH, IS, IHS) 264
Mucopolysaccharidosis Type II (Hunter Syndrome A, B; MPS IIA, IIB) 264
Mucopolysaccharidosis Type III (Sanfilippo Syndrome A, B, C, D; MPS IIIA, IIIB, IIIC, IIID) 264
Mucolipidoses 266
Mucolipidosis Type I (ML I, Sialidosis Type I, Sialidosis Type II, Neuraminidase Deficiency, Cherry-Red Spot Myoclonus Syndrome) 266
Mucolipidosis Type II (ML II, Inclusion-cell (I-cell) Disease) and Mucolipidosis Type III (ML III, Pseudo-Hurler Polydystrophy) 268
Mucolipidosis Type II, Also Referred to as I-Cell Disease 268
Mucolipidosis Type III (Pseudo-Hurler Polydystrophy) 268
Mucolipidosis Type IV (ML IV, Sialolipidosis) 268
Niemann–Pick Disease (Sphingomyelin Lipidosis) 269
Tay–Sachs Disease (GM2 Gangliosidosis, Type I) 270
Sandhoff Disease (GM2 Gangliosidosis, Type II) 271
Multiple Sulfatase Deficiency 271
Gaucher Disease 272
Female Carrier of Gaucher Disease 273
Acquired Pediatric Conditions 275
Shaken Baby Syndrome 275
Suggested Reading 277
Retinopathy of Prematurity 277
Persistent Fetal Vasculature Syndrome 277
Congenital Folds 277
Neurofibromatosis Type I 277
Neurofibromatosis Type 2 277
Combined Hamartoma of the Retina and RPE 277
Wyburn Mason Syndrome 277
Congenital Retinal Macrovessel 277
von Hippel–Lindau Syndrome 277
Retinal Cavernous Hemangioma 277
Leber Congenital Amaurosis 277
Neuronal Ceroid Lipofuscinoses 277
Mucopolysaccharidoses 277
Mucolipidoses 277
Niemann–Pick Disease 277
Tay–Sachs Disease 277
Sandhoff Disease 277
Multiple Sulfatase Deficiency 278
Gaucher Disease 278
Shaken Baby Syndrome 278
4 Inflammation 279
White Dot Syndromes 280
Multiple Evanescent White Dot Syndrome (MEWDS) 280
Multifocal Choroiditis (MFC) (Punctate Inner Choroidopathy (PIC), Multifocal Choroiditis and Panuveitis (MCP), Idiopathic Progressive Subretinal Fibrosis Syndrome) 290
Acute Zonal Occult Outer Retinopathy (AZOOR) 300
Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) 309
Serpiginous Choroiditis 321
Relentless Placoid Chorioretinitis (Ampiginous Choroiditis) 326
Persistent Placoid Maculopathy 328
Birdshot Chorioretinopathy 332
Macular Manifestations in Birdshot Chorioretinopathy 335
Diseases Simulating Birdshot Chorioretinopathy 335
Birdshot Chorioretinopathy and Chorioretinal Atrophy 336
Overlapping “White Dot” Syndromes 340
Multiple Evanescent White Dot Syndrome (MEWDS) and Acute Macular Neuroretinopathy (AMN) 340
MEWDS and AZOOR 341
MFC and MEWDS 342
AZOOR and MFC 344
APMPPE and MEWDS 346
Lymphoma Simulating a “White Dot” Syndrome 347
Systemic Disease with Retinal Vasculitis 348
Pars Planitis 348
Multiple Sclerosis 350
Behçet Disease 351
Inflammatory Bowel Disease 354
Crohn’s Disease 354
Ulcerative Colitis 355
Seronegative Spondyloarthropathies 356
Rheumatological Diseases 357
Scleroderma 357
Churg–Strauss Syndrome (Allergic Granulomatosis and Angiitis) 358
Relapsing Polychondritis 359
Adult-Onset Still’s Disease 359
Idiopathic Retinal Vasculitis, Aneurysms, and Neuroretinitis (IRVAN) 360
Idiopathic Frosted-Branch Angiitis 362
Sarcoidosis 367
Systemic Disease with Choroidopathy 373
Vogt–Koyanagi–Harada Syndrome 373
Sympathetic Ophthalmia 385
Systemic Disease with Scleritis 390
Scleritis 390
Idiopathic Uveal Scleral Granuloma 396
Suggested Reading 397
Multiple Evanescent White Dot Syndrome 397
Multifocal Choroiditis (MFC) (Punctate Inner Choroidopathy (PIC), Multifocal Choroiditis and Panuveitis (MCP), Idiopathic Progressive Subretinal Fibrosis Syndrome) 397
Acute Zonal Occult Outer Retinopathy 397
Acute Posterior Multifocal Placoid Pigment Epitheliopathy 397
Serpiginous Choroiditis 397
Relentless Placoid Chorioretinitis (Ampiginous Choroiditis) 397
Persistent Placoid Maculopathy 397
Birdshot Chorioretinopathy 397
Pars Planitis 397
Multiple Sclerosis 398
Behçet Disease 398
Inflammatory Bowel Disease/Crohn’s Disease/Ulcerative Colitis 398
Seronegative Spondyloarthropathies 398
Scleroderma 398
Churg-Strauss Syndrome (Allergic Granulomatosis and Angiitis) 398
Relapsing Polychondritis 398
Adult-Onset Still’s Disease 398
Idiopathic Retinal Vasculitis, Aneurysms, and Neuroretinitis 398
Idiopathic Frosted-Branch Angiitis 398
Sarcoidosis 398
Vogt–Koyanagi–Harada Syndrome 398
Scleritis 398
Idiopathic Uveal Scleral Granuloma 398
5 Infection 399
Viruses 400
Human Immunodeficiency Virus (HIV) Associated Retinopathy 400
Cytomegalovirus Retinitis 401
Acute Retinal Necrosis Syndrome 406
Acute Retinal Necrosis Syndrome: Herpes Simplex Type 1 408
Acute Retinal Necrosis Syndrome: Herpes Simplex Type 2 408
Progressive Outer Retinal Necrosis 411
Epstein–Barr Virus Retinitis 415
Rubeola Virus: Subacute Sclerosing Pancencephalitis (SSPE) 416
Congenital Rubella Syndrome 417
Coxsackievirus 417
Acute Retinal Pigment Epitheliitis 417
Acute Idiopathic Maculopathy 418
Rift Valley Virus 421
West Nile Virus 421
Dengue Virus Maculopathy 424
Protozoa 425
Toxoplasmosis 425
Congenital Toxoplasmosis Scars 425
Acute Toxoplasmic Lesions 426
Miliary Toxoplasmosis 428
Toxoplasmosis with Kyrieleis Plaques 429
Toxoplasmosis and Choroidal Neovascularization 430
Giardiasis 431
Bacteria 431
Leprosy 431
Tuberculosis 432
Nocardiosis 439
Whipple Disease 441
Bartonella: Cat-Scratch Disease 442
Spirochetes 452
Syphilis 452
Acute Syphilitic Posterior Placoid Chorioretinitis 453
Optic Neuritis 454
Chorioretinitis 454
Vasculitis 455
Vitritis 458
Frosted Angiitis 460
Resolved Chorioretinitis 461
Leptospirosis 462
Fungi 463
Candida albicans Chorioretinitis 463
Aspergillosis 464
Cryptococcosis 465
Presumed Ocular Histoplasmosis Syndrome (POHS) 467
Blastomycosis 469
Ocular Coccidioidomycosis 470
Fusarium Keratitis, Vitritis, and Retinal Papillitis 472
Pneumocystis carinii 472
Nematodes 473
Cysticercosis 473
Subretinal Cysticercosis 474
Neural Cysticercosis 474
Diffuse or Disseminated Unilateral Subacute Neuroretinitis 475
Toxocariasis 478
Filariasis 480
Alaria Mesocercariae 482
Ophthalmomyiasis 484
Gnathostomiasis 486
Angiostrongyliasis 487
Ascariasis 487
Suggested Reading 488
HIV Associated Retinopathy 488
Cytomegalovirus Retinitis 488
Acute Retinal Necrosis Syndrome 488
Dengue Virus Maculopathy 489
Toxoplasmosis 489
Giardiasis 489
Leprosy 489
Tuberculosis 489
Nocardiosis 489
Whipple Disease 489
Bartonella: Cat-Scratch Disease 489
Syphilis 490
Pneumocystis carinii 490
Candida albicans Chorioretinitis 490
Aspergillosis 490
Cryptococcosis 490
Histoplasmosis 491
Ocular Coccidioidomycosis 491
Blastomycosis 491
Fusarium Keratitis, Vitritis, and Retinal Papillitis 491
Cysticercosis 491
Diffuse or Disseminated Unilateral Subacute Neuroretinitis 491
Toxocariasis 491
Filariasis 491
Myiasis (Ophthalmomyiasis/Gnathostomiasis/Angiostrongyliasis/Alaria Mesocercariae) 492
6 Retinal Vascular Disease 493
Congenital Abnormalities 495
Macrovessel 495
Prepapillary Vascular Loop 495
Familial Retinal Arterial Tortuosity 496
Retinal Arterial Occlusions 497
Ophthalmic Artery Occlusion 497
Central Retinal Artery Occlusion 498
Central Retinal Artery Occlusion with Sparing of the Ciliary Artery 500
Branch Retinal Artery Occlusion 501
Multiple Branch Artery Occlusions 502
Recurrent Retinal Artery Occlusions 503
Embolus Distalization 503
PAMM (Paracentral Acute Middle Maculopathy) 504
PAMM versus CWS 504
PAMM Associated with BRAO 505
Cilioretinal Artery Occlusion 507
Plaques 508
Retinal Venous Occlusions 509
Central Retinal Vein Occlusion 509
Wyburn–Mason Syndrome and Central Retinal Vein Occlusion 512
CRVO and Cilioretinal Artery Occlusion 512
CRVO and PAMM 513
Collateralization 514
Carotid Cavernous Fistula and Central Retinal Vein Occlusion 515
Natural Course 516
Treatment: Laser Photocoagulation 516
Treatment: Intravitreal Anti-VEGF Therapy 517
Branch Retinal Vein Occlusions 518
Compensatory Collateralization 520
Treatment: Laser Photocoagulation 522
Treatment: Intravitreal Pharmacotherapy 522
Retinal Arteriolar Macroaneurysm 524
Treatment: Laser 526
Treatment: Anti-VEGF Therapy 527
Coats Disease and Macular Telangiectasia Type I (Congenital Telangiectasia, Leber Miliary Aneurysms) 527
Treatment: Laser 534
Treatment: Anti-VEGF Therapy 539
Macular Telangiectasia Type 2 (Idiopathic Perifoveal Telangiectasia, Idiopathic Juxtafoveal Telangiectasis Type 2) 540
Pigment Hyperplasia 546
Crystals 547
Subretinal Neovascularization 549
Treatment 551
Radiation Retinopathy 553
Eales Disease (Idiopathic Peripheral Vascular Occlusive Disease) 557
Retinal Vascular Manifestations of Systemic Disease 562
Hypertensive Retinopathy 562
Diabetic Retinopathy 566
Nonproliferative Diabetic Retinopathy 566
Proliferative Diabetic Retinopathy 569
Peripheral Ischemia and Neovascularization 569
Disc Neovascularization 572
Vitreous Hemorrhage 573
Fibrous Proliferation 574
Diabetic Papillopathy 577
Macular Manifestations of Diabetic Retinopathy 578
Macular Edema 578
Macular Ischemia 579
Macular Hole 579
Choroidal Neovascularization 580
Retinal Hemorrhage 580
Exudative Lipid Maculopathy 581
Macular Scar 581
Exudative Detachment 581
Pre-Retinal Fibrosis 582
Tractional Retinal Detachment 583
Diabetic Retinopathy and Systemic Disease 583
Hypertension 583
Diabetes and Blood Dyscrasia 584
Diabetes and Waldenström Macroglobulinemia 584
Lipemia Retinitis 585
Treatment: Laser Photocoagulation 586
Macular Lipid and Edema 586
Retinal Break 587
Neovascularization 588
Treatment: Vitreoretinal Surgery 591
Treatment: Intravitreal Anti-VEGF Therapy 592
Rubeosis Iridis 594
Sickle-Cell Retinopathy 595
Macular Manifestations 599
Detachment 601
Hyperlipidemia 602
Ocular Ischemic Syndrome 603
Takayasu Arteritis (Takayasu Disease) 606
Polycythemia Vera 609
Essential Thrombocytosis 610
Hyperviscosity Syndrome from Leukemia 610
Waldenström Macroglobulinemia 611
Multiple Myeloma 612
Hypereosinophilic Syndrome 615
Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, Skin Changes (POEMS Syndrome) 615
Hyperhomocysteinemia 616
Protein C and Protein S Deficiency 616
Antithrombin III Deficiency 618
Factor V Leiden 618
Thrombotic Thrombocytopenic Purpura 619
Disseminated Intravascular Coagulation 620
Systemic Lupus Erythematosus 621
Lupus Choroidopathy 626
Lupus and Malignant Hypertension 628
Giant Cell Arteritis (Temporal Arteritis) 628
Polyarteritis Nodosa 630
Churg–Strauss Syndrome 630
Dermatomyositis 631
Granulomatosis with Polyangiitis (Wegener’s Granulomatosis) 631
Weber–Christian Disease (Nodular Panniculitis) 633
Systemic Sclerosis 633
Antiphospholipid Antibody Syndrome (Hughes Syndrome) 634
Cardiac Myxomas 635
Susac Syndrome 636
Purtscher Retinopathy 637
Pregnancy 638
Central Serous Chorioretinopathy 638
Preeclampsia 640
Lupus Erythematosus 642
Protein S Deficiency 642
Iatrogenic Embolization 643
Suggested Reading 646
Macrovessel 646
Retinal Tortuosity 646
Prepapillary Vascular Loop 646
Retinal Artery Occlusions 646
PAMM versus CWS 646
Retinal Venous Occlusions 646
Retinal Arteriolar Macroaneurysm 646
Coats Disease and Macular Telangiectasia Type I (Congenital Telangiectasia, Leber Miliary Aneurysms) 647
Macular Telangiectasia Type 2 (Idiopathic Perifoveal Telangiectasia, Idiopathic Juxtafoveal Telangiectasis Type 2) 647
Radiation Retinopathy 647
Eales Disease (Idiopathic Peripheral Vascular Occlusive Disease) 647
Hypertensive Retinopathy 647
Diabetic Retinopathy 647
Sickle-Cell Retinopathy 648
Hyperlipidemia 648
Ocular Ischemic Syndrome 648
Takayasu Arteritis (Takayasu Disease) 648
Polycythemia Vera 648
Essential Thrombocythemia 648
Hyperviscosity Syndrome from Leukemia 648
Waldenström Macroglobulinemia 648
Multiple Myeloma 649
Hypereosinophilic Syndrome 649
Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gamnopathy (POEMS Syndrome) 649
Hyperhomocysteinemia 649
Protein C and Protein S Deficiency 649
Antithrombin III Deficiency 649
Factor V Leiden 649
Thrombotic Thrombocytopenic Purpura 649
Disseminated Intravascular Coagulopathy 649
Systemic Lupus Erythematosus 649
Giant Cell Arteritis (Temporal Arteritis) 649
Polyarteritis Nodosa 649
Churg–Strauss Syndrome 649
Dermatomyocytis 650
Granulomatosis with Polyangiitis (Wegner’s Granulomatosis) 650
Systemic Sclerosis 650
Antiphospholipid Antibody Syndrome (Hughes Syndrome) 650
Cardiac Myxomas and Chorioretinal Occlusions 650
Susac Syndrome 650
Purtscher Retinopathy 650
7 Degeneration 651
Vitreous 653
Vitreous Synchisis and Syneresis 653
Posterior Vitreous Detachment 654
Asteroid Hyalosis 656
Vitreous Amyloidosis 659
Vitreous Cyst 661
Angioid Streaks 662
Pseudoxanthoma Elasticum 663
Pattern Dystrophy 667
Subretinal Fluid and Acquired Vitelliform Lesions 669
Choroidal Neovascularization 670
Trauma 671
Fibrous Scarring 672
Pathologic Myopia 674
Staphyloma 676
Radial Tracts and Myopic Staphyloma 681
Dome-Shaped Macula 682
Myopic Macular Degeneration 683
Myopic Retinoschisis 685
Lacquer Cracks 686
Myopic Stretch Lines 688
Subretinal Hemorrhages 689
Choroidal Neovascularization 690
Multifocal Choroiditis 692
Peripapillary Choroidal Thickening and Cavitation 695
Age-Related Macular Degeneration 696
Non-neovascular AMD 697
Drusen 697
Drusen with Pigmentary Abnormalities 701
Drusen with Refractile Deposits 702
Unilateral Drusen 703
Peripheral Drusen 703
Spontaneous Resolution of Drusen 704
Cuticular Drusen 705
Large Colloid Drusen 708
Reticular Pseudodrusen 709
Pigment Epithelial Detachment 711
Drusenoid PED 711
Drusenoid PED Variants 712
Mixed Drusenoid and Serous PED 712
Serous PED 713
Serous PED Variants 714
Acquired Vitelliform Lesions 715
Acquired Vitelliform Lesions in Drusen and PED 716
Acquired Vitelliform Lesions in Cuticular Drusen 717
Acquired Vitelliform Lesions in Reticular Pseudodrusen 718
Acquired Vitelliform Lesions in Non-AMD Entities 718
Natural Course of Acquired Vitelliform Lesions 719
Geographic Atrophy 722
Outer Retinal Tubulation 724
Age-Related Choroidal Atrophy 725
Outer Retinal Corrugations 726
Neovascular Age-Related Macular Degeneration 727
Optical Coherence Tomography Angiography of Neovascularization 728
Type 1 Neovascularization 729
Vascularized PED variants 734
Multilayered PED 734
The “onion sign” 735
Retinal Pigment Epithelium Tears 736
Polypoidal Choroidal Vasculopathy 739
Natural Course 743
Polypoidal Choroidal Vasculopathy and Polypoidal Neovascularization 750
Peripheral Exudative Hemorrhagic Chorioretinopathy 752
Type 2 Neovascularization 753
Type 3 Neovascularization 754
Vasogenic sequence (left) 754
Alternative hypothesis (below) 754
Disciform Scarring 758
Idiopathic Choroidal Neovascularization 759
Suggested Reading 760
8 Oncology 763
Pediatric Mass Lesions of the Fundus 764
Retinoblastoma 765
Retinoblastoma Classification 766
International Classification of Retinoblastoma 767
Group A Retinoblastoma 767
Group B Retinoblastoma 767
Group C Retinoblastoma 767
Group D Retinoblastoma 767
Group E Retinoblastoma 767
Retinoblastoma Growth Patterns 768
Retinoblastoma Variations 769
Retinoblastoma Diagnostic Testing 770
Retinoblastoma Features 771
Regression of Retinoblastoma Following Plaque Radiotherapy 772
Regression of Retinoblastoma Following Intravenous Chemotherapy 773
Regression of Retinoblastoma Following Intra-arterial Chemotherapy 774
Management of Retinoblastoma with Enucleation 775
Retinoblastoma Pathology 776
Retinoblastoma Pathology—High Risk for Metastasis 777
Teratoma 778
Klippel–Trenaunay–Weber Syndrome 779
Medulloepithelioma 780
Retinal Astrocytic Hamartoma 782
Acquired Retinal Astrocytoma 785
Retinal Acquired Astrocytoma with Exudative Retinopathy 786
Retinal Hemangioblastoma (Capillary Hemangioma) 787
Obvious Endophytic Juxtapapillary Retinal Hemangioblastoma 790
Subtle Intraretinal Juxtapapillary Retinal Hemangioblastoma 790
Retinal Hemangioblastoma Management 792
Endophytic Juxtapapillary Retinal Hemangioblastoma 794
Hemangioblastoma with Extensive Fibrosis 795
Retinal Cavernous Hemangioma 796
Variations in Presentation 797
Retinal Racemose Hemangioma 799
Retinal Vasoproliferative Tumor 804
Retinal Vasoproliferative Tumor in Retinitis Pigmentosa 807
Combined Hamartoma of the Retina and Retinal Pigment Epithelium 808
Diffuse Retinal Hamartoma in Neurofibromatosis Type 2 808
Enhanced Depth Imaging Optical Coherence Tomography of Combined Hamartoma 814
Congenital Hypertrophy of the Retinal Pigment Epithelium (CHRPE) 815
CHRPE in the Macula 816
Spectrum of CHRPE 817
Multifocal CHRPE (Bear Tracks) 818
Polar Bear Tracks 819
CHRPE with Nodular Adenoma/Adenocarcinoma (Epithelioma) 820
Pigmented Ocular Fundus Lesions with Familial Adenomatous Polyposis 821
Congenital Simple Hamartoma of the Retinal Pigment Epithelium 822
Adenoma/Adenocarcinoma (Epithelioma) of the Retinal Pigment Epithelium 823
Torpedo Maculopathy of the Retinal Pigment Epithelium 824
Unilateral Dysgenesis of the Retinal Pigment Epithelium 825
Choroidal Nevus 826
The Clinical Spectrum of Choroidal Nevus 827
Ocular Melanocytosis 828
Optical Coherence Tomography of Retinal Pigment Epithelial Abnormalities Overlying Choroidal Nevus 829
Optical Coherence Tomography of Retinal Pigment Epithelial Abnormalities Overlying Choroidal Nevus 830
Spectral Domain Optical Coherence Tomography of Choroidal Nevus 831
Suspicious Giant Choroidal Nevus 832
Growth of Choroidal Nevus into Choroidal Melanoma 833
Choroidal Melanoma 834
Choroidal Melanoma: Morphological Variations 834
American Joint Commission on Cancer (AJCC) Clinical Classification of Posterior Uveal Melanoma (7th edition) 835
Choroidal Melanoma Size Variations 837
Choroidal Melanoma with Pigmentary Variations 838
Factors for Early Detection of Choroidal Melanoma 841
Early Detection of Choroidal Melanoma 843
Early Detection of Small Choroidal Melanoma Using Mnemonic “To Find Small Ocular Melanoma Using Helpful Hints Daily” 844
Choroidal Melanoma Before and After Plaque Radiotherapy 846
Choroidal Metastasis 847
Solitary Choroidal Metastasis in Patients with Carcinoma 849
Bilateral Choroidal Metastasis 852
Management of Choroidal Metastasis 853
Bilateral Diffuse Uveal Melanocytic Proliferation 854
Choroidal Hemangioma 858
Choroidal Hemangioma in the Macular Region 859
Choroidal Hemangioma Treated with Photodynamic Therapy 861
Diffuse Choroidal Hemangioma 862
Choroidal Osteoma 864
Optical Coherence Tomography of Choroidal Osteoma 868
Idiopathic Sclerochoroidal Calcification 870
Bartter Syndrome and Sclerochoroidal Calcification 871
Choroidal Leiomyoma 872
Intraocular Lymphoma 873
Paraneoplastic Cloudy Vitelliform Maculopathy 875
Choroidal Lymphoma Masquerading as Age-Related Macular Degeneration in a 59-year-old Man 876
Benign Uveal Lymphoid Hyperplasia 877
Mucosal-Associated Lymphoid Tumor (MALT Syndrome) 880
Enhanced Depth Imaging Spectral Domain Optical Coherence Tomography of Choroidal Lymphoma 881
Variations in Lymphoma Presentations 882
Large-Cell Lymphoma Infiltrating in the Retina and Optic Nerve 884
Vitreous, Retinal, Choroidal, and Optic Nerve Involvement in Ocular CNS Lymphoma 885
Intraocular Metastatic Testicular Lymphoma 886
Treatment of Choroidal Lymphoma with External-Beam Radiotherapy 887
Tumors of the Optic Disc 889
Melanocytoma of the Optic Disc 889
Growth of Astrocytic Hamartomas of the Optic Nerve in Tuberous Sclerosis 892
Lymphoma of the Optic Nerve 894
Hemangioblastoma (Capillary Hemangioma) of the Optic Disc 896
Optic Disc Hemangioblastoma with Macular Schisis 897
Optic Disc Hemangioblastoma with Macular Hole 898
Cavernous Hemangioma 898
Metastasis to the Optic Disc 899
Optic Disc Metastasis in Breast Cancer 899
Optic Disc Metastasis in Lung Cancer 899
Optic Disc Metastasis from Gastric Carcinoma 899
Leukemia 900
Spectral Domain Optical Coherence Tomography of Intraocular Leukemia 903
Perifoveal Ischemia with Leukemia 904
Scattered Hemorrhages and Leukemia 904
Exudative Detachment in Leukemia 906
Disc Infiltration and Leukemia 906
Pre-retinal Infiltration in Leukemia 906
Infection and Leukemia 906
Vitreous Hemorrhage and Leukemia 907
Diabetic Retinopathy and Leukemia 908
Suggested Reading 909
Retinoblastoma 909
Retinal Astrocytic Hamartoma/Acquired Retinal Astrocytoma 909
Retinal Hemangioblastoma/Capillary Hemangioma 909
Retinal Cavernous Hemangioma 909
Retinal Racemose Hemangioma 909
Retinal Vasoproliferative Tumor 909
Congenital Hypertrophy of the Retinal Pigment Epithelium (CHRPE) 910
Pigmented Ocular Fundus Lesions with Familial Adenomatous Polyposis 910
Congenital Simple Hamartoma of the Retinal Pigment Epithelium 910
Torpedo Maculopathy of the Retinal Pigment Epithelium 910
Combined Hamartoma of the Retina and Retinal Pigment Epithelium 910
Adenoma/Adenocarcinoma (Epithelioma) of the Retinal Pigment Epithelium 910
Ciliary Body Pigment Epithelium Epithelioma (Adenoma/Adenocarcinoma) 910
Medulloepithelioma 910
Choroidal Nevus 910
Choroidal Melanoma 911
Choroidal Metastasis 911
Choroidal Hemangioma 911
Choroidal Osteoma 911
Idiopathic Sclerochoroidal Calcification 911
Choroidal Leiomyoma 912
Intraocular Lymphoma 912
Melanocytoma of the Optic Disc 912
Hemangioblastoma (Capillary Hemangioma) of the Optic Disc 912
9 Vitreomacular Traction, Epiretinal Membranes, and Macular Holes 913
Epiretinal Membrane 914
Spontaneous Release of Epiretinal Membrane 919
Surgical Treatment 920
10 Central Serous Chorioretinopathy and Other Exudative Detachments 937
Central Serous Chorioretinopathy 938
Fluorescein Angiography in CSC 938
Smokestack Leak 938
Mushroom or Umbrella Leak 939
Inkblot Leak 940
Indocyanine Green Angiography in CSC 940
Optical Coherence Tomography (OCT) in CSC 942
Pigment Epithelial Detachment (PED) 942
Cystoid Macular Degeneration 943
Fundus Autofluorescence (FAF) in CSC 943
CSC Simulating Age-Related Macular Degeneration (AMD) 946
Asymptomatic Eye 946
Chronic Central Serous Chorioretinopathy 947
Fibrin in CSC 948
PED Microrip (Blow-Out) in CSC 950
RPE Rip in CSC 950
Bullous-Dependent Detachment in CSC 951
Treatment 952
Photodynamic Therapy and CSC 952
Unusual CSC Cases 955
Pachychoroid Disease 958
Pachychoroid Pigment Epitheliopathy 958
Pachychoroid Neovasculopathy 960
Optical Coherence Tomography Angiography of Pachychoroid Neovasculopathy 961
Acute Exudative Polymorphous Vitelliform Maculopathy 962
Idiopathic Uveal Effusion Syndrome 964
Isolated Posterior Uveal Effusion 966
Idiopathic Organ Transplant Chorioretinopathy 967
Suggested Reading 968
11 Peripheral Retinal Degenerations and Rhegmatogenous Retinal Detachment 969
Peripheral Retinal Abnormalities 970
Retinal Holes 970
Lattice Degeneration 971
Retinal Tears and Localized Detachments 973
Retinal Detachments 974
Chronic Retinal Detachment With Demarcation Lines 976
Chronic Retinal Detachment with Retinal Macrocyst 977
Retinal Dialysis and Giant Retinal Tear (GRT) 978
Retinal Detachment and Macular Hole 980
Proliferative Vitreoretinopathy (PVR) 981
Retinoschisis 983
Juvenile X-Linked Retinoschisis 987
Optic Nerve Pit with Macular Schisis Detachment 988
Treatment of Retinal Detachment 990
Retinal Detachment: Postsurgery 992
Macular Translocation Surgery 999
Suggested Reading 1000
Peripheral Retinal Abnormalities 1000
Lattice Degeneration 1000
Retinal Tears and Localized Detachments 1000
Retinal Detachments 1000
Retinal Detachments Following Cataract Surgery 1000
Retinal Dialysis and Giant Retinal Tear (GRT) 1000
Retinoschisis 1001
Optic Nerve Pit with Macular Schisis Detachment 1001
Treatment of Retinal Detachment 1001
12 Traumatic Chorioretinopathy 1003
Direct Ocular Injury (Nonpenetrating and/or Nonperforating) 1004
Berlin’s Edema (Commotio Retinae) 1004
Traumatic Retinal Pigment Epitheliopathy 1006
Traumatic Macular Hole 1008
Choroidal Rupture 1011
Traumatic Retinal Breaks and Detachments 1014
Chorioretinitis Sclopetaria 1016
Optic Nerve Avulsion 1018
Open-Globe Injury 1019
Intraocular Foreign Body (IOFB) 1019
Penetrating and/or Perforating Ocular Injury 1020
Indirect Ocular Injury 1022
Valsalva Retinopathy 1022
Purtscher Retinopathy 1024
Terson Syndrome 1025
Shaken Baby Syndrome 1025
Solar and/or Laser-Induced Retinopathy 1026
Altitude Retinopathy 1028
Suggested Reading 1029
Berlin’s Edema (Commotio Retinae) 1029
Traumatic Retinal Pigment Epitheliopathy 1029
Traumatic Macular Hole 1029
Choroidal Rupture 1029
Traumatic Retinal Breaks and Detachments 1029
Chorioretinitis Sclopetaria 1030
Optic Nerve Avulsion 1030
Intraocular Foreign Body 1030
Penetrating and/or Perforating Injury 1030
Valsalva Retinopathy 1031
Purtscher Retinopathy 1031
Terson Syndrome 1031
Shaken Baby Syndrome 1031
Solar Retinopathy and/or Laser-Induced Retinopathy 1032
Altitude Retinopathy 1032
13 Complications of Ocular Surgery 1033
Injections 1034
Retrobulbar Anesthetic 1034
Nasopharynx Injection 1035
Intravitreal Triamcinolone Injection 1036
Intravitreal Vancomycin Injection 1036
Mechanical Retinal Vascular Obstruction (from Injections) 1037
Optic Nerve Sheath Injection 1037
Retrobulbar Hemorrhage 1039
Choroidal Ischemia (Outer Retinal Infarction) 1040
Antibiotic Toxicity During Intraocular Surgery 1042
Intraocular Aminoglycosides 1042
Intracameral Vancomycin 1045
Decompression Retinopathy 1046
Non-Arteritic Anterior Ischemic Optic Neuropathy 1047
Phototoxicity 1048
Hypotony 1050
Choroidal Hemorrhage 1051
Spontaneous Choroidal Hemorrhage with Polypoidal Choroidal Vasculopathy (PCV) after Cataract Surgery 1055
Surgical Materials and Devices 1056
Titanium Tack 1056
Silicone Oil 1056
Intraocular Gas 1056
Perfluorocarbon (PFC) Liquid 1057
Dislocated Implant 1057
Lens Fragment 1057
Retinal Prosthesis 1058
Transpupillary Thermotherapy (TTT) 1058
Cryodemarcation 1059
Photodynamic Therapy (PDT) 1059
Retinal Cyst on Buckle 1060
Macular Folds Status Post Scleral Buckling Surgery 1060
Giant Retinal Pigment Epithelial Tear 1061
Extrusion of Buckle 1061
Laser of Calcific Plaque Arteriole Occlusion 1061
Suggested Reading 1062
Injections 1062
Outer Retinal Infarction 1062
Cryodemarcation 1062
Aminoglycoside Toxicity 1062
Intracameral Vancomycin 1062
Dislocated Intraocular Lens/ Retained Lens Fragment 1062
Extrusion of Scleral Buckle 1062
Decompression Retinopathy 1062
Non-Arteritic Anterior Ischemic Optic Neuropathy/Ischemia 1063
Phototoxicity 1063
Hypotony 1063
Choroidal Hemorrhage 1063
Silicone Oil/Perfluorocarbon (PFC) Liquid 1063
Retinal Tacks 1063
Diamond/Steel Particles 1063
Retinal Prosthesis 1063
Transpupillary Thermotherapy 1063
Photodynamic Therapy 1064
14 Chorioretinal Toxicities 1065
Introduction 1067
Disruption of the Retinal Pigment Epithelium 1067
Chloroquine Derivatives 1067
Chloroquine 1067
Hydroxychloroquine 1070
Phenothiazines 1072
Thioridazine 1072
Chlorpromazine 1076
Dideoxyinosine (DDI) 1077
Clofazimine 1078
Deferoxamine 1078
Chemotherapeutic Agents 1079
Denileukin Diftitox 1079
MEK Inhibitors 1080
Vascular Damage or Occlusion 1081
Quinine Sulfate 1081
Oral Contraceptives 1082
Ergot Alkaloids 1082
Procainamide 1083
Cocaine Abuse 1083
Heparin 1086
Interferon 1086
Chemotherapeutic Agents 1088
Gemcitabine 1088
Cystoid Macular Edema and/or Retinal Edema/Folds 1089
Nicotinic Acid 1089
Drug-Induced Myopia 1090
Sulfa Antibiotics, Hydrochlorothiazine, Acetazolamide, Topiramate 1090
Imatinib Mesylate 1091
Glitazones 1092
Pioglitazone 1092
Ritonavir 1092
Chemotherapeutic Agents 1093
Paclitaxel, Docetaxel 1093
Albumin-Bound Paclitaxel 1093
Crystalline Retinopathy 1094
Tamoxifen 1094
Methoxyflurane 1096
Canthaxanthin 1098
Nitrofurantoin 1100
West African Crystalline Maculopathy 1100
Talc Retinopathy 1101
Uveitis 1103
Cidofovir 1103
Rifabutin 1103
Optic Neuropathy 1104
Carbon Monoxide 1104
Fludarabine 1104
Methanol 1105
Miscellaneous 1105
Vitamin A Deficiency 1105
Celiac Disease 1106
Digoxin 1106
Suggested Reading 1107
Chloroquine 1107
Hydroxychloroquine 1107
Thioridazine 1107
Chlorpromazine 1107
Deferoxamine 1108
MEK Inhibitors 1108
Quinine Sulfate 1108
Oral Contraceptives 1108
Ergot Alkaloids 1108
Nicotinic Acid 1108
Drug-Induced Myopia 1108
Tamoxifen 1108
Methoxyflurane 1109
Canthaxanthine 1109
Nitrofurantoin 1109
Talc Retinopathy 1109
Cidofovir 1109
Rifabutin 1109
Cardiac Glycosides 1109
Methanol 1109
15 Congenital and Developmental Anomalies of the Optic Nerve 1111
Abnormalities of Optic Nerve Size 1113
Optic Nerve Hypoplasia 1113
Megalopapilla 1114
Optic Nerve Aplasia 1114
Vascular Abnormalities 1115
Congenital Prepapillary Vascular Loops 1115
Persistent Fetal Vasculature (PFV) 1116
Bergmeister Papilla 1117
Congenital Retinal Macrovessel 1117
Cilioretinal Artery Occlusion 1118
Excavated and Colobomatous Defects 1119
Optic Nerve, Retinochoroidal, and Iris Colobomas 1119
Morning Glory Disc Anomaly 1122
Optic Nerve Pit 1123
Situs Inversus 1126
Tilted Disc Syndrome 1126
Peripapillary Staphyloma 1128
Optic Nerve Head Drusen 1129
Optic Nerve Head Drusen with Juxtapapillary Choroidal Neovascularization (CNV) 1133
Optic Nerve Trauma 1135
Select Optic Nerve Ischemic, Inflammatory, and Infectious Processes 1137
Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) 1137
Optic Nerve Papillitis 1138
Acute Neuroretinitis (Bartonella henselae) 1138
Leber Idiopathic Stellate Neuroretinitis 1139
Chronic Papillitis 1139
Ocular Syphilis 1140
Idiopathic Intracranial Hypertension (IIH) 1140
Optic Nerve Tumors 1141
Optic Nerve Glioma 1141
Meningioma of the Optic Nerve 1141
Metastatic Tumors of the Optic Nerve 1142
Optic Nerve Melanocytoma 1142
Retinal Capillary Hemangioma 1143
Retinal Capillary Hemangioma of the Optic Nerve Head 1144
Racemose Hemangioma 1144
Astrocytic Hamartoma 1146
Combined Hamartoma of Retina and Retinal Pigment Epithelium (RPE) 1147
Retinoblastoma 1149
Paraneoplastic Disorders 1150
Other Anomalies of the Optic Nerve 1151
Myelinated Nerve Fibers (MNF) 1151
Suggested Reading 1153
General References 1153
Optic Nerve Hypoplasia 1153
Megalopapilla 1153
Optic Nerve Aplasia 1153
Congenital Prepapillary Vascular Loops 1153
Persistent Fetal Vasculature 1153
Bergmeister Papilla 1154
Congenital Retinal Macrovessel 1154
Cilioretinal Artery Occlusion 1154
Optic Nerve, Retinochoroidal, and Iris Colobomas 1155
Morning Glory Disc Anomaly 1155
Optic Nerve Pit 1156
Tilted Disc Syndrome 1156
Peripapillary Staphyloma 1156
Optic Nerve Head Drusen 1157
Optic Nerve Trauma 1157
Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) 1157
Optic Nerve Papillitis 1158
Acute Neuroretinitis (Bartonella henselae) 1158
Idiopathic Intracranial Hypertension (IIH) 1158
Ocular Syphilis 1159
Optic Nerve Glioma 1159
Meningioma of the Optic Nerve 1159
Retinal Capillary Hemangioma and Hemangioma of the Optic Nerve Head 1160
Racemose Hemangioma 1160
Optic Nerve Melanocytoma 1160
Astrocytic Hamartoma 1161
Combined Hamartoma of Retina and RPE 1161
Retinoblastoma 1162
Paraneoplastic Disorders 1162
Myelinated Nerve Fibers (MNF) 1162
Index 1163
A 1163
B 1163
C 1164
D 1165
E 1166
F 1166
G 1166
H 1167
I 1167
J 1167
K 1168
L 1168
M 1168
N 1169
O 1169
P 1170
Q 1171
R 1171
S 1172
T 1172
U 1173
V 1173
W 1173
X 1173
Z 1173
IBC_Clinical Key advert IBCi