Ultra Widefield Imaging of the Retina.

Format:

Book

Author/Creator:

Cicinelli, Febo.

Contributor:

Bandello, Febo.

Language:

English

Physical Description:

1 online resource (366 pages)

Edition:

1st ed.

Place of Publication:

Academic Press [Imprint] March 2025 San Diego : Elsevier Science & Technology Books Saint Louis : Elsevier [Distributor] Saint Louis : Elsevier [Distributor] Saint Louis : Elsevier [Distributor]

Chantilly : Elsevier Science & Technology, 2025.

Summary:

Ultra Widefield Imaging of the Retina covers basic anatomy and physiology of the retina, providing the technical aspects of ultra widefield retinal imaging that give readers a strong grounding in the discipline's central tenets.

Contents:

Front Cover

Ultra Widefield Imaging of the Retina

Copyright

Dedication

Contents

Contributors

About the editors

Foreword

Preface

List of abbreviations

1 - Introduction to ultra widefield retina imaging and technical aspects

1. Introduction

2. What is UWF and WF imaging?

3. Historical background: From traditional fundus cameras to UWF imaging devices

4. Modern digital UWF imaging systems

4.1 Optos

4.2 Heidelberg Spectralis

4.3 Zeiss Clarus

4.4 iCare Eidon with UWF module

4.5 Which one is the best?

4.5.1 Peripheral extension and color fidelity

4.5.2 Image quality and sharpness

4.5.3 Color fundus versus pseudocolor

5. Clinical utility of UWF imaging

5.1 Elevating diagnostic precision: Lessons learned from diabetic retinopathy

5.2 Documenting and monitoring

5.3 Guide precise and targeted treatments

5.4 Telemedicine and screening

References

2 - Anatomy, physiology, and imaging of the normal retina

1. Retinal topography and anatomic landmarks

2. Chorioretinal circulation and oxygenation

3. Color fundus photography

4. Fundus autofluorescence imaging

4.1 Basic principle and mechanism of autofluorescence

4.2 Are all autofluorescence the same?

5. Fluorescein angiography

5.1 Basic principle and mechanism of fluorescence

5.2 Advances in fluorescein angiography technique

5.3 Interpretation of a normal fluorescein angiogram

5.4 Abnormal fluorescein angiogram

6. Indocyanine green angiography

6.1 Interpretation of a normal indocyanine green angiogram

6.1.1 Early phase

6.1.2 Middle phase (3-15min)

6.1.3 Late phase (15-60min)

6.2 Abnormal indocyanine green angiogram

3 - Vascular chorioretinal disorders

1. Diabetic retinopathy

1.1 UWF and DR staging.

1.2 UWF-FA and DR severity

1.3 UWF and DME

1.4 UWF and neovascular complications

1.5 UWF and DR progression

1.6 UWF and treatment response

1.7 UWF and DR screening

2. Retinal artery occlusions

3. Retinal vein occlusions

3.1 UWF and peripheral ischemia

3.2 UWF-FA and cystoid macular edema

3.3 UWF and treatment response

4. Hypertensive retinopathy, choroidopathy, and optic neuropathy

5. Sickle cell retinopathy

6. Terson syndrome

7. Valsalva retinopathy

8. Carotid-cavernous fistula

9. Hyperviscosity syndrome

10. Ocular ischemic syndrome

4 - Degenerative chorioretinal disorders

1. Age-related macular degeneration

1.1 Dry age-related macular degeneration

1.2 Neovascular age-related macular degeneration

2. Peripheral exudative hemorrhagic chorioretinopathy

3. Pachychoroid spectrum and venous overload choroidopathy

3.1 Simple CSC

3.2 Complex CSC

3.3 Peripapillary pachychoroid syndrome

3.4 Bullous CSC

4. Pathologic myopia

5. Commotio retinae

6. Stellate multiform amelanotic choroidopathy

7. Dense deposit disease

8. Extensive macular atrophy with pseudodrusen-like appearance

9. Sclerochoroidal calcification

10. Uveal effusion syndrome

11. Stellate nonhereditary idiopathic foveomacular retinoschisis

5 - Inherited chorioretinal disorders

2. Retinitis pigmentosa

3. Choroideremia

4. Gyrate atrophy

5. Enhanced S-cone syndrome

6. Flecked retina disorders

7. Leber congenital amaurosis and early-onset severe retinal dystrophy

8. Cone and cone-rod dystrophies

9. Stargardt disease

10. Peripherinopathies

11. Bestrophinopathies

11.1 Peripheral retinal findings in best vitelliform macular dystrophy and autosomal recessive bestrophinopathy

12. X-linked retinoschisis.

13. Pseudoxanthoma elasticum

14. Mitochondrial retinopathies

15. Other fundus dystrophies

15.1 Bietti crystalline dystrophy

15.2 Familiar foveal retinoschisis

15.3 Late-onset retinal degeneration

15.4 Sorsby fundus dystrophy

6 - Pediatric and developmental conditions

1. Coats' disease

2. Retinopathy of prematurity

3. Familial exudative vitreoretinopathy

4. Persistent fetal vasculature

5. Congenital optic disc anomalies

5.1 Optic disc coloboma

5.2 Optic disc pit

5.3 Morning Glory syndrome

6. Congenital rubella syndrome

7. Albinism

8. Systemic associations

8.1 Alport syndrome

8.2 Stickler syndrome

8.3 Dyskeratosis congenita

9. Phakomatosis

9.1 Neurofibromatosis type 1

9.2 Tuberous sclerosis

10. Myelinated nerve fibers

11. Retinal arteriovenous malformation

7 - Vitreoretinal conditions

1. Rhegmatogenous peripheral retinal lesions

2. Nonrhegmatogenous peripheral retinal lesions

3. Rhegmatogenous retinal detachment

3.1 Pre-operative evaluation

3.2 Nonsurgical intervention

3.3 Surgical approaches for RRD

4. Tractional retinal detachment and proliferative vitreoretinopathy

5. Macular vitreoretinal diseases

6. Ocular gene therapy and prosthesis

8 - Inflammatory disorders

1. Infectious inflammatory diseases

1.1 Syphilis

1.2 Tuberculosis

1.3 Whipple's disease

1.4 Acute retinal necrosis

1.5 Cytomegalovirus retinitis

1.6 West Nile Virus

1.7 Coxsackie retinopathy

1.8 Toxoplasmosis

1.9 Toxocariasis

1.10 Diffuse unilateral subacute neuroretinitis

1.11 Endophthalmitis

2. Noninfectious inflammatory diseases

2.1 Pars planitis

2.2 Sarcoidosis

2.3 Retinal vasculitis

2.4 Vogt-Koyanagi-Harada disease

2.5 Sympathetic ophthalmia

2.6 Birdshot chorioretinopathy.

3. White dot syndromes

3.1 Multiple evanescent white dot syndrome

3.2 Idiopathic multifocal choroiditis/punctate inner choroidopathy

3.3 Secondary white dot syndromes

3.4 Placoid diseases

3.5 Serpiginous choroiditis

3.6 AZOOR and MORR

4. Posterior scleritis

9 - Chorioretinal tumors

1. Choroidal melanocytic lesions

1.1 Choroidal nevi

1.2 Choroidal melanoma

1.3 Melanocytoma

2. Choroidal hemangioma

3. Choroidal metastasis

4. Choroidal lymphoma

5. Choroidal osteoma

6. Retinal vascular tumors

6.1 Retinal capillary hemangioblastoma

6.2 Cavernous hemangiomas

6.3 Vasoproliferative tumors

7. Retinoblastoma

8. Benign retinal tumors

8.1 Congenital hypertrophy of the RPE

8.2 Congenital grouped albinotic spots

8.3 Combined hamartoma of the retina and RPE

8.4 Astrocytic hamartomas

8.5 Focal scleral nodule

9. Retinal paraneoplastic syndromes

9.1 Cancer-associated retinopathy

9.2 Melanoma-associated retinopathy

9.3 Bilateral diffuse uveal melanocytic proliferation

9.4 Acute exudative polymorphous vitelliform maculopathy

10. Vitreoretinal lymphoma

11. Leukemic retinopathy, Purtscher retinopathy and Purtscher-like retinopathy

11.1 Leukemic retinopathy

11.2 Purtscher and Purtscher-like retinopathy

12. Radiation retinopathy and optic neuropathy

10 - Toxic retinopathies

1. Hydroxychloroquine

2. Didanosine toxicity

3. Poppers maculopathy

4. MEK inhibitors

5. Check-point inhibitors

6. Brolucizumab

7. Taxane retinopathy

8. Pentosan polysulfate sodium toxicity

9. Gentamicin toxicity

10. Light toxicity

11. Vitamin A deficiency

Index

Back Cover.

Notes:

Description based on publisher supplied metadata and other sources.

ISBN:

0-443-29085-7

OCLC:

1519831071