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9783540200451

Uveitis And Immunological Disorders

by ;
  • ISBN13:

    9783540200451

  • ISBN10:

    3540200452

  • Format: Hardcover
  • Copyright: 2004-12-16
  • Publisher: Springer Verlag
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Summary

Uveitis and immunological disorders encompass a wide spectrum of potentially blinding diseases that are seen in daily practice by many ophthalmologists. In recent years enormous progress has been made understanding the principal mechanisms of inflammatory and immunological processes in ocular disorders. The purpose of this volume of Essentials in Ophthalmology is to provide the ophthalmologist with our present understanding of the pathogenesis of the most frequent immune-mediated disorders of the eye and a practical approach to these diseases. Uveitis and Immunological Disorders fits in the series of Essentials in Ophthalmology to fill the gap between textbooks and original research publications. With a broad spectrum of contributions, including diseases affecting the conjunctiva, sclera and cornea as well as intraocular inflammation, this publication will serve not only as a valuable source of up-to-date information for ophthalmologists but also be of interest to pediatricians, specialists in internal medicine and dermatologists confronted with inflammatory eye diseases. Although mainly focused on clinical aspects of inflammatory eye diseases, several contributions address aspects such as immune mechanisms and genetics of these diseases.

Table of Contents

Targets in Ocular Allergy
Alessandra Micera
Sergio Bonini
Alessandro Lambiase
Roberto Sgrulletta
Stefano Bonini
Introduction
1(1)
Chronic Allergic Eye Diseases
2(1)
Effector Cells and Cytokine Release
2(1)
Chemokines and Adhesion Molecules
3(1)
Neuropeptide and Growth Factor Involvement
4(1)
Tissue Remodelling and the Contribution of Fibroblasts
5(1)
Metabolism of Extracellular Matrix
6(1)
Conclusions
7(4)
References
8(3)
Dry Eye: Inflammation of the Lacrimal Functional Unit
Stephen C. Pflugfelder
Michael E. Stern
Introduction
11(3)
Basics
11(1)
Lacrimal Functional Unit
12(2)
Specific Pathologies of the Lacrimal Functional Unit
14(2)
Dysfunction of the Afferent System
14(1)
Dysfunction of the Efferent System
15(1)
Glandular Dysfunction
15(1)
Lacrimal Keratoconjunctivitis Inflammation
16(3)
Corneal Epithelial Disease
17(1)
Conjunctival Epithelial Disease
17(1)
Inflammation
18(1)
Diagnosis
19(2)
Therapies
21(4)
References
22(3)
Ocular Cicatricial Pemphigoid
Ahmed Muna
C. Stephen Foster
Introduction
25(1)
Pathophysiology
26(1)
Epidemiology
26(1)
Clinical History
26(1)
Clinical Signs
26(1)
Staging
27(1)
Diagnosis
28(1)
Laboratory Tests
28(1)
Conjunctival Biopsy
28(1)
Histology
29(1)
Treatment
29(4)
Medical
29(2)
Surgery
31(2)
Collaborative Care
33(1)
Prognosis
33(2)
References
34(1)
Immunomodulation for Corneal Transplantation
Douglas J. Coster
Keryn A. Williams
Introduction
35(1)
Why Has Corneal Transplantation Fallen Behind Solid Organ Grafting?
36(1)
Immunomodulation for Corneal Transplantation
36(1)
Actuarial Survival Data on Corneal Transplantation
37(1)
Options for Immunomodulation
38(1)
Corneal Privilege
38(1)
Mechanisms of Corneal Allograft Rejection
39(1)
The Afferent Limb: Sensitization to Corneal Alloantigens
39(1)
The Efferent Limb: Histological Correlates
40(1)
Current Approaches to Immunomodulation for Corneal Transplantation
41(4)
Anti-inflammatory Measures
41(1)
Atraumatic Microsurgical Technique
41(1)
Topical Corticosteroids
41(1)
HLA Matching for Class I and Class II Antigens
41(1)
Systemic Immunosuppression
42(1)
Systemic Corticosteroids
42(1)
Antiproliferative Agents
43(1)
Calcineurin Blockers
43(1)
Combination Therapy
44(1)
Side Effects of Systemic Immunosuppression
44(1)
Novel Approaches to Immunomodulation
45(1)
Monoclonal Antibody Fragments
45(1)
Gene Therapy
45(1)
Conclusion
46(6)
References
46(6)
Scleritis
Alisa Kim
Sean Dumars
Samir Shah
Bartly Mondino
Introduction
52(5)
Classification
52(3)
Anatomy
55(1)
Pathogenesis
55(1)
Histopathology
56(1)
Clinical Presentation
57(5)
History: Ocular Symptoms
57(1)
Physical Examination: Ocular Signs
58(2)
Associated Ocular Manifestations
60(1)
Systemic Diseases: Clinical Evaluation
61(1)
Diagnostic Tools
62(1)
Medical Management
63(1)
Surgical Management
64(3)
References
65(2)
Clinical Aspects of MALT
Erich Knop
Nadja Knop
Uwe Pleyer
Introduction
67(1)
Structure and Function of MALT
68(8)
Structure of MALT
68(3)
Eye-Associated Lymphoid Tissue (EALT)
71(3)
Basic Functions of MALT
74(2)
Dry Eye Disease
76(5)
Introduction
75(1)
Epidemiology, Definition and Characteristics of Dry Eye
76(4)
Novel Therapeutic Approaches to Dry Eye Disease
80(1)
Ocular Allergy
81(3)
Introduction
81(1)
Epidemiology, Definition and Characteristics of Allergic Eye Disease
81(3)
Course and Therapy Options in Allergic Ocular Disease
84(1)
Keratoplasty
84(7)
Introduction
84(1)
Immunological Characteristics of Keratoplasty
85(2)
References
87(4)
Immunogenetics of Ocular Inflammatory Disease
Ralph D. Levinson
Introduction
91(2)
Human Leukocyte Antigens
93(3)
HLA Nomenclature
94(1)
Class I HLA
94(1)
Class II HLA
95(1)
HLA Haplotypes and Linkage Disequilibrium
95(1)
HLA and Disease Pathogenesis
95(1)
HLA Associations with Ocular Inflammatory Disease
96(5)
Class I HLA Associations with Ocular Inflammatory Disease
96(2)
Class II HLA Associations with Ocular Inflammatory Disease
98(2)
HLA Associations with Ocular Infections
100(1)
HLA Associations with External Ocular Inflammation
100(1)
HLA Associations with Extraocular Disease
100(1)
Non-HLA Genes Associated with Ocular Inflammatory Disease
101(1)
Other Ocular Diseases
102(1)
Conclusion
102(7)
References
102(7)
Immune Mechanisms in Uveitis
Ling Chen
Lynn K. Gordon
Introduction
109(1)
Animal Uveitis Models
110(7)
Experimental Autoimmune Uveitis (EAU)
110(6)
Endotoxin-Induced Uveitis (EIU)
116(1)
Experimental Melanin-Protein-Induced Uveitis (EMIU)
116(1)
Experimental Autoimmune Pigment Epithelial Membrane Protein-Induced Uveitis (EAPU)
117(1)
Immune Mechanisms in Human Uveitis
117(8)
HLA-Associated Human Uveitis
117(2)
Behcet's Disease
119(1)
Vogt-Koyanagi-Harada Syndrome
120(1)
References
121(4)
The Tip of the Iceberg: Current Knowledge of Uveitis in Juvenile Arthritis
Uwe Pleyer
Claudia Sengler
Natasa Orlic
Rolf Keitzer
Introduction
125(1)
Classification of Arthritis
126(1)
Epidemiology
126(1)
Pathogenesis
127(1)
Risk Factors for the Development of Uveitis in JRA
128(1)
Clinical Features of Uveitis in JCA
128(1)
Complications of Uveitis in JCA
129(1)
Macula Edema
130(1)
Differential Diagnosis
130(1)
Prognostic Factors for Uveitis
131(2)
Gender
132(1)
Type of Arthritis
132(1)
Onset of Arthritis
132(1)
Severity of Uveitis at-Onset
132(1)
Correlation of Uveitis and Arthritis Activity
133(1)
Treatment of Uveitis in JCA
133(3)
Topical Steroid Treatment
133(1)
Nonsteroidal Anti-inflammatory Drugs (NSAID)
134(1)
Systemic Immunomodulatory Agents
134(2)
Recommendations for Ocular Screening in JCA
136(5)
References
136(5)
Herpes Viruses in Ocular Inflammation
Bahram Bodaghi
Phuc LeHoang
Introduction
141(2)
Fundamental Virology
143(1)
Epidemiology
143(1)
Pathophysiology
144(1)
Experimental Viral Uveitis
144(1)
Experimental Models to Study Viral Retinitis
145(1)
Clinical Features
145(5)
Anterior Uveitis
145(2)
Viral Retinopathies
147(2)
Differential Diagnosis
149(1)
Putative Viral-Associated Uveitis
150(1)
Diagnosis
150(3)
Obtention of Ocular Fluids
151(1)
Herpes Viruses
151(1)
Search for Antiviral Antibodies
152(1)
Treatment
153(8)
Anterior Uveitis
153(1)
Viral Retinopathies
154(3)
References
157(4)
Cytomegalovirus and the Eye
Marc D. de Smet
Introduction
161(1)
Populations at Risk
161(2)
HIV Associated Immunosuppression
161(1)
Immunosuppression in Non-HIV Settings
162(1)
Appearance and Course
163(3)
Manifestation Prior to Initial Treatment
163(1)
Manifestations Under Therapy
164(1)
Differential Diagnosis
165(1)
Investigations
166(1)
Therapeutic Agents
166(1)
Ganciclovir
166(1)
Valganciclovir
167(1)
Foscarnet
167(1)
Other Agents
167(1)
Screening and Treatment Algorithms
167(1)
CMV in HIV Infected Patients
168(1)
CMV in Other Immunosuppressive States
168(1)
Management of Complications
168(5)
Immune Recovery
168(1)
Retinal Detachment
168(1)
References
169(4)
Behcet's Disease
Manfred Zierhut
Nicole Stubiger
Christoph Deuter
Ina Kotter
Introduction
173(1)
Definition and Epidemiology of BD
174(4)
Definition
174(1)
History
174(1)
Epidemiology
174(4)
Genetics of BD
178(4)
Immunology
182(2)
T Cells
182(1)
NK Cells
183(1)
Neutrophils
183(1)
Endothelial Dysfunction
183(1)
Coagulation and Fibrinolytic Pathway Abnormalities
184(1)
General (Extraocular) Manifestations of BD
184(3)
Oral Aphthous Ulcerations
184(1)
Genital Ulcerations
185(1)
Skin Lesions
185(1)
Pathergy Phenomenon
185(1)
Skeletal System
185(1)
Gastrointestinal Manifestations
186(1)
Neurological Manifestations
186(1)
Vascular Manifestations
186(1)
Rare Manifestations
187(1)
Life Expectancy
187(1)
Ocular Involvement
187(3)
Anterior Segment Changes
188(1)
Posterior Segment Changes
188(1)
Complications
189(1)
Diagnosis
190(1)
Therapy
190(12)
Local Treatment
191(1)
Systemic Treatment
191(3)
Surgical Treatment
194(1)
Practical Treatment Recommendations
194(1)
References
195(7)
Choroiditis: General Considerations and Classification
Carl P. Herbort
Introduction
202(1)
Indocyanine Green Angiography (ICGA)
202(4)
Physicochemical Properties of Indocyanine Green (ICG)
202(2)
Standard ICG Angiographic Protocol for Inflammatory Diseases
204(1)
Principles for the Interpretation of ICGA [9, 10]
204(1)
Differences Between Fluorescein and Indocyanine Green Angiography
205(1)
Clinico-pathologic-angiographic Correlations
205(1)
Relevance of ICGA in Ocular Inflammatory Diseases
205(1)
The Concepts of Inflammatory Choriocapillaropathy and Stromal Choroiditis [12]
206(4)
Primary Inflammatory Choriocapillaropathy (PICCP)
206(1)
Stromal Choroiditis
207(1)
Secondary Inflammatory Choriocapillaropathy
207(1)
References
207(3)
Primary Inflammatory Choriocapillaropathies
Luca Cimino
Alessandro Mantovani
Carl. P. Herbort
Introduction
210(1)
Angiographic Signs in Inflammatory Choriocapillaropathies
211(2)
Angiographic Signs in Inflammatory Choriocapillaropathies
213(1)
Patient History, Systemic and Ocular Symptoms and Signs in Primary Inflammatory Choriocapillaropathies
213(1)
Practical Attitude in Primary Inflammatory Choriocapillaropathies (PICCP)
214(1)
Specific Entities
215(9)
Multiple Evanescent White Dot Syndrome (MEWDS)
215(1)
Acute Idiopathic Blind Spot Enlargement (AIBSE)
216(1)
Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) or Acute Multifocal Ischaemic Choriocapillaropathy (AMIC)
217(2)
Multifocal Choroiditis (MFC), Including Punctate Inner Choroiditis (PIC), Diffuse Subretinal Fibrosis and Presumed Ocular Histoplasmosis Syndrome (POHS)
219(3)
Serpiginous Choroiditis
222(2)
Rare Entities
224(2)
Acute Zonal Occult Outer Retinopathy (AZOOR) and Acute Annular Outer Retinopathy (AAOR)
224(1)
Acute Macular Neuroretinopathy (AMN)
225(1)
Overlapping Clinical Pictures in PICCPs: The Choriocapillaris as the Common Denominator of PICCPs
226(2)
Association of Different PICCPs in the Same Patient
226(1)
Intermediary Forms of PICCP
226(1)
Unclassifiable Primary Inflammatory Choriocapillaropathies
227(1)
Conclusion
228(5)
References
228(5)
Stromal Choroiditis
Nadia Bouchenaki
Carl O. Herbort
Introduction
233(22)
Specific Entities
234(1)
Primary Stromal Choroiditis
234(9)
Stromal Choroiditis as a Random Involvement of a Systemic Disease
243(6)
Other Infectious Choroiditides
249(2)
References
251(4)
Immunomodulatory Therapy in Uveitis
Stephan R. Thurau
Gerhild Wildner
Introduction
255(2)
Cytotoxic Drugs
257(4)
Azathioprine
258(1)
Methotrexate
258(1)
Mycophenolate Mofetil
259(1)
Leflunomide
259(1)
Cyclophosphamide
259(1)
Chlorambucil
260(1)
Antibiotics
261(1)
Sulphasalazine
261(1)
Calcineurin Inhibitors
261(1)
Cyclosporine A (CsA)
261(1)
Tacrolimus (FK506)
262(1)
Sirolimus (Rapamycin)
262(1)
Immunomodulatory Substances
262(4)
Thalidomide
262(1)
Anti-TNF-α Treatment
263(2)
Interferon-α
265(1)
Daclizumab
266(1)
Oral Tolerance Induction
266(7)
Retinal Autoantigens as Tolerogens
266(1)
HLA-peptide B27PD as Oral Tolerogen
267(1)
References
268(5)
Vitrectomy in Uveitis
Matthias D. Becker
Arnd Heiligenhaus
Marc De Smet
Janet Davis
Introduction
273(1)
General Approach to PPV in Uveitis
273(1)
Patient Selection
273(1)
Timing of Surgery
273(1)
Technical Considerations
274(1)
Diagnostic Procedures
274(1)
Perioperative Management
274(3)
Assessment of Other Ocular Disease
274(1)
Concomitant Medical Management
275(2)
Combined Surgery
277(2)
Cataract Surgery
277(1)
Membrane Peeling
278(1)
Cryotherapy
278(1)
Diagnostic PPV
278(1)
Postoperative Complications
279(1)
Hypotony
279(1)
Retinal Detachment
279(1)
Vitreous Haemorrhage
280(1)
Uveitis Recurrence
280(1)
PPV in Specific Diseases
280(5)
Fuchs Uveitis Syndrome
280(1)
Behcet's Disease
280(1)
Intermediate Uveitis
280(1)
Childhood Uveitis
281(1)
Infectious Uveitis
281(2)
References
283(2)
Subject Index 285

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