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دسته بندی: بیماری ها: طب داخلی ویرایش: نویسندگان: Peizeng Yang سری: ISBN (شابک) : 9811537259, 9789811537257 ناشر: Springer Singapore سال نشر: 2020 تعداد صفحات: 855 زبان: English فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) حجم فایل: 181 مگابایت
در صورت تبدیل فایل کتاب Atlas of Uveitis: Diagnosis and Treatment به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب اطلس یووئیت: تشخیص و درمان نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
این اطلس اطلاعات پیشرفته ای را در مورد یووئیت ارائه می دهد که نشان دهنده یک دستاورد بزرگ در مطالعات بالینی در مورد یووئیت است. این شامل بیش از سه هزار عکس تصویربرداری از بیماران یووئیت است که مشخصات کامل بیماری و طیف تغییراتی که معمولاً با آن مواجه میشوند را نشان میدهد. رژیم های درمانی متعددی نیز ارائه شده است که هر کدام برای فرم خاصی از یووئیت طراحی شده اند. اطلس همچنین آخرین پیشرفتها در مطالعات یووئیت را در خود جای داده است و آن را به منبعی منحصربفرد و ارزشمند برای خوانندگان وسیعی از جمله چشم پزشکان، دانشجویان تحصیلات تکمیلی، دانشجویان پزشکی و پزشکان در چشم پزشکی تبدیل میکند.
This Atlas provides cutting-edge information on uveitis, which represents a major achievement in clinical studies on uveitis. It includes more than three thousand imaging photos of uveitis patients, showing the disease’s complete profile and the spectrum of variations commonly encountered. Numerous therapeutic regimens are also presented, each of which is designed for a specific form of uveitis. The Atlas also incorporates the latest advances in uveitis studies, making it a unique and valuable resource for a broad readership, including ophthalmologists, postgraduate students, medical students and doctors in ophthalmology.
Foreword by Quan Dong Nguyen Foreword by Aize Kijlstra Foreword by Shigeaki Ohno Foreword by Manfred Zierhut Foreword by Amod Gupta Preface Contents Part I: Overview 1: Anatomy and Physiology of Uveitis 1.1 Anatomy of the Eyeball 1.2 Eye Content 1.3 The Cornea 1.4 The Sclera 1.5 The Uveal Tract 1.6 The Retina 1.7 The Aqueous Humor 1.8 The Lens 1.9 The Vitreous References 2: Classification of Uveitis 2.1 Classification of Uveitis 2.2 Anatomic Classification 2.3 Classification Based on Course 2.4 Classification Based on Clinical and Pathological Features 2.5 Classification Based on Causative Agents References Part II: Diagnosis of Uveitis 3: History-Taking in Uveitis Patients 3.1 Overview 3.2 Geographical and Racial Distribution of Uveitis 3.3 Age at Onset of Uveitis 3.4 Sex Distribution in Uveitis 3.5 Unilateral or Bilateral Involvement 3.6 Family History 3.7 Personal History 3.8 Systemic Manifestations (Systemic Disorders) References 4: Ocular Examinations 4.1 The Purposes of Ocular Examinations in Uveitis Patients 4.2 Visual Acuity 4.3 Lid Changes May Be Associated with the Following Entities of Uveitis 4.4 Conjunctival Changes May Be Seen in the Following Uveitis Entities 4.5 Episcleritis 4.6 Scleritis 4.7 Red Reflex Through the Sclera 4.8 Corneal Changes 4.9 Ciliary Injection 4.10 Keratic Precipitates (KPs) 4.11 Anterior Chamber Alterations 4.12 Changes in the Iris and Pupil 4.13 Changes of the Anterior Chamber Angle 4.14 Changes of the Lens 4.15 Changes of the Vitreous 4.16 The Fundus Changes in Uveitis References 5: Auxiliary Ocular Examinations 5.1 Ultrasound Biomicroscopy (UBM) 5.1.1 Overview 5.1.2 The Changes Disclosed by UBM in Uveitis Patients 5.2 Ultrasonography 5.2.1 Overview 5.2.2 The Changes Detected by Ultrasonography in Uveitis Patients 5.3 Fundus Fluorescein Angiography (FFA) 5.3.1 Overview 5.3.2 The Changes Detected by FFA in Uveitis Patients 5.4 Indocyanine Green Angiography (ICGA) 5.4.1 Overview 5.4.2 The Changes Detected by ICGA in Uveitis Patients 5.5 Optical Coherence Tomography (OCT) Imaging 5.5.1 Overview 5.5.2 The Changes Disclosed by OCT in Uveitis Patients References 6: Systemic Imaging and Laboratory Investigations 6.1 X-ray 6.2 Computed Tomography (CT) 6.3 Magnetic Resonance Imaging (MRI) 6.4 Laboratory Investigations References Part III: Treatment of Uveitis 7: Ideology, Fundamental Principles, and Strategies in Management of Uveitis 7.1 Ideology in Uveitis Management 7.2 Fundamental Principles 7.3 Strategies References 8: Corticosteroids 8.1 Overview 8.2 Topical Corticosteroids 8.3 Periocular Corticosteroids 8.4 Intravitreal Corticosteroids 8.5 Systemic Corticosteroids References 9: Steroid-sparing Immunosuppressive Agents 9.1 Overview 9.2 Cyclophosphamide 9.3 Chlorambucil 9.4 Cyclosporine A (CsA) 9.5 FK506 9.6 Methotrexate 9.7 Azathioprine 9.8 Mycophenolate Mofetil 9.9 Biological Agents References 10: Non-steroidal Anti-inflammatory Drugs 10.1 Overview 10.2 Topical NSAIDs 10.3 Systemic NSAIDs References 11: Complications and Their Management 11.1 Overview 11.2 Cataract 11.3 Ocular Hypertension and Glaucoma 11.4 Macular Edema References Part IV: Specific Uveitis Entities, Scleritis and Episcleritis 12: Acute Anterior Uveitis 12.1 Definition 12.2 Epidemiology 12.3 Common Entities 12.4 Less Common Entities 12.5 Symptoms 12.6 Signs 12.7 Complications 12.8 Diagnosis 12.9 Differential Diagnosis 12.10 Treatment 12.11 Prognosis References 13: Intermediate Uveitis 13.1 Definition 13.2 Epidemiology 13.3 Etiology and Pathogenesis 13.4 Clinical Manifestations 13.4.1 Symptoms 13.4.2 Signs 13.5 Complications 13.6 Diagnosis 13.7 Differential Diagnosis 13.8 Treatment 13.9 Prognosis References 14: Posterior Uveitis 14.1 Definition 14.2 Epidemiology 14.3 Etiology and Pathogenesis 14.4 Entities of Posterior Uveitis 14.5 Diagnosis and Differential Diagnosis 14.6 Treatment 14.7 Prognosis References 15: Uveitis Associated with Ankylosing Spondylitis 15.1 Definition 15.2 Epidemiology 15.3 Etiology and Pathogenesis 15.4 Systemic Manifestations 15.5 Ocular Manifestations 15.6 Complications 15.7 Diagnosis 15.8 Differential Diagnosis 15.9 Treatment 15.10 Prognosis References 16: Uveitis Associated with Reactive Arthritis 16.1 Definition 16.2 Epidemiology 16.3 Systemic Manifestations 16.4 Ocular Manifestations 16.5 Diagnosis 16.6 Differential Diagnosis 16.7 Treatment 16.8 Prognosis References 17: Uveitis Associated with Psoriasis 17.1 Definition 17.2 Epidemiology 17.3 Etiology and Pathogenesis 17.4 Systemic Manifestations 17.5 Ocular Manifestations 17.6 Complications 17.7 Diagnosis 17.8 Differential Diagnosis 17.9 Treatment 17.10 Prognosis References 18: Uveitis Associated with Inflammatory Bowel Diseases 18.1 Definition 18.2 Epidemiology 18.3 Etiology and Pathogenesis 18.4 Systemic Manifestations 18.5 Ocular Manifestations 18.6 Complications 18.7 Diagnosis 18.8 Differential Diagnosis 18.9 Treatment 18.10 Prognosis References 19: Anterior Uveitis Associated with Herpesviruses 19.1 Definition 19.2 Epidemiology 19.3 Etiology and Pathogenesis 19.4 Clinical Manifestations 19.5 Complications 19.6 Diagnosis 19.7 Differential Diagnosis 19.8 Treatment 19.9 Prognosis References 20: Fuchs Syndrome 20.1 Definition 20.2 Epidemiology 20.3 Etiology and Pathogenesis 20.4 Clinical Manifestations 20.5 Complications 20.6 Diagnosis 20.7 Differential Diagnosis 20.8 Treatment 20.9 Prognosis References 21: Posner–Schlossman Syndrome 21.1 Definition 21.2 Epidemiology 21.3 Etiology and Pathogenesis 21.4 Clinical Manifestations 21.5 Complications 21.6 Diagnosis 21.7 Differential Diagnosis 21.8 Treatment 21.9 Prognosis References 22: Uveitis in Children 22.1 Definition 22.2 Epidemiology 22.3 Specific Concerns About Uveitis in Children 22.4 Complications 22.5 Diagnosis 22.6 Treatment 22.7 Prognosis References 23: Uveitis-associated with Juvenile Idiopathic Arthritis 23.1 Definition 23.2 Epidemiology 23.3 Etiology and Pathogenesis 23.4 Systemic Manifestations 23.5 Ocular Manifestations 23.6 Complications 23.7 Diagnosis 23.8 Differential Diagnosis 23.9 Treatment 23.10 Prognosis References 24: Blau Syndrome 24.1 Definition 24.2 Etiology and Pathogenesis 24.3 Systemic Manifestations 24.4 Ocular Manifestations 24.5 Complications 24.6 Diagnosis 24.7 Differential Diagnosis 24.8 Treatment 24.9 Prognosis References 25: Tubulointerstitial Nephritis and Uveitis Syndrome 25.1 Definition 25.2 Epidemiology 25.3 Etiology and Pathogenesis 25.4 Clinical Manifestations 25.5 Diagnosis 25.6 Differential Diagnosis 25.7 Treatment 25.8 Prognosis References 26: Behcet’s Disease 26.1 Definition 26.2 Epidemiology 26.3 Etiology and Pathogenesis 26.4 Ocular Lesions 26.5 Extraocular Manifestations 26.6 Ocular Complications 26.7 Diagnosis 26.8 Diagnostic Criteria 26.9 Differential Diagnosis 26.10 Treatment 26.11 Prognosis References 27: Vogt–Koyanagi–Harada Disease 27.1 Definition 27.2 Epidemiology 27.3 Etiology and Pathogenesis 27.4 Clinical Manifestations 27.4.1 Ocular Manifestations [1, 11] 27.4.2 Extraocular Manifestations [1–4] 27.4.3 Manifestations in Different Stages [1, 4, 12] 27.5 Complications 27.6 Auxiliary Examinations 27.7 Diagnosis 27.8 Differential Diagnosis 27.9 Treatment 27.10 Prognosis References 28: Sympathetic Ophthalmia 28.1 Definition 28.2 Epidemiology 28.3 Etiology and Pathogenesis 28.4 Ocular Manifestations 28.5 Extraocular Manifestations 28.6 Complications 28.7 Diagnosis 28.8 Differential Diagnosis 28.9 Management 28.10 Prognosis References 29: Retinal Vasculitis 29.1 Definition 29.2 Retinal Vasculitis Associated with Systemic Vasculitis 29.3 Retinal Vasculitis Secondary to Infectious Diseases 29.4 Primary Retinal Vasculitis 29.5 Clinical Manifestation 29.5.1 Symptoms 29.5.2 Signs 29.6 Complications 29.7 Diagnosis 29.8 Differential Diagnosis 29.9 Management 29.10 Prognosis References 30: Eales Disease 30.1 Definition 30.2 Epidemiology 30.3 Etiology and Pathogenesis 30.4 Clinical Manifestations 30.4.1 Symptoms 30.4.2 Signs 30.5 Complications 30.6 Diagnosis 30.7 Differential Diagnosis 30.8 Treatment 30.9 Prognosis References 31: Frosted Branch Angiitis 31.1 Definition 31.2 Epidemiology 31.3 Etiology and Pathogenesis 31.4 Clinical Manifestations 31.5 Complications 31.6 Diagnosis 31.7 Differential Diagnosis 31.8 Treatment 31.9 Prognosis References 32: Ocular Sarcoidosis 32.1 Definition 32.2 Epidemiology 32.3 Etiology and Pathogenesis 32.4 Systemic Manifestations 32.5 Ocular Manifestations 32.6 Diagnosis and Diagnostic Criteria 32.7 Differential Diagnosis 32.8 Treatment 32.9 Prognosis References 33: Systemic Lupus Erythematosus 33.1 Definition 33.2 Epidemiology 33.3 Etiology and Pathogenesis 33.4 Systemic Manifestations 33.5 Ocular Manifestations 33.6 Diagnosis 33.7 Differential Diagnosis 33.8 Treatment 33.9 Prognosis References 34: Uveitis Associated with Relapsing Polychondritis 34.1 Definition 34.2 Epidemiology 34.3 Etiology and Pathogenesis 34.4 Ocular Manifestations 34.5 Systemic Manifestations 34.6 Diagnosis 34.7 Treatment 34.8 Prognosis References 35: Subretinal Fibrosis and Uveitis Syndrome 35.1 Definition 35.2 Epidemiology 35.3 Etiology and Pathogenesis 35.4 Clinical Manifestations 35.5 Diagnosis 35.6 Differential Diagnosis 35.7 Treatment 35.8 Prognosis References 36: Multifocal Choroiditis and Panuveitis 36.1 Definition 36.2 Epidemiology 36.3 Etiology and Pathogenesis 36.4 Clinical Manifestations 36.5 Complications 36.6 Diagnosis 36.7 Differential Diagnosis 36.8 Treatment 36.9 Prognosis References 37: Serpiginous Choroiditis 37.1 Definition 37.2 Epidemiology 37.3 Etiology and Pathogenesis 37.4 Clinical Manifestations 37.5 Complications 37.6 Diagnosis 37.7 Differential Diagnosis 37.8 Treatment 37.9 Prognosis References 38: Acute Retinal Pigment Epitheliitis 38.1 Definition 38.2 Epidemiology 38.3 Etiology and Pathogenesis 38.4 Clinical Manifestations 38.5 Diagnosis 38.6 Differential Diagnosis 38.7 Treatment 38.8 Prognosis References 39: Punctate Inner Choroidopathy 39.1 Definition 39.2 Epidemiology 39.3 Etiology and Pathogenesis 39.4 Clinical Manifestations 39.5 Diagnosis 39.6 Differential Diagnosis 39.7 Treatment 39.8 Prognosis References 40: Birdshot Chorioretinopathy 40.1 Definition 40.2 Epidemiology 40.3 Etiology and Pathogenesis 40.4 Clinical Manifestations 40.5 Complications 40.6 Diagnosis 40.7 Differential Diagnosis 40.8 Treatment 40.9 Prognosis References 41: Acute Posterior Multifocal Placoid Pigment Epitheliopathy 41.1 Definition 41.2 Epidemiology 41.3 Etiology and Pathogenesis 41.4 Clinical Manifestations 41.5 Diagnosis 41.6 Differential Diagnosis 41.7 Treatment 41.8 Prognosis References 42: Multiple Evanescent White Dot Syndrome 42.1 Definition 42.2 Epidemiology 42.3 Etiology and Pathogenesis 42.4 Clinical Manifestations 42.5 Diagnosis 42.6 Differential Diagnosis 42.7 Treatment and Prognosis References 43: Ocular Tuberculosis 43.1 Definition 43.2 Epidemiology 43.3 Etiology and Pathogenesis 43.4 Clinical Manifestations 43.5 Complications 43.6 Diagnosis 43.7 Differential Diagnosis 43.8 Treatment 43.9 Prognosis References 44: Syphilitic Uveitis 44.1 Definition 44.2 Epidemiology 44.3 Etiology and Pathogenesis 44.4 Phasing of Syphilis 44.5 Ocular Manifestations 44.6 Complications 44.7 Diagnosis 44.8 Differential Diagnosis 44.9 Treatment 44.10 Prognosis References 45: Ocular Toxoplasmosis 45.1 Definition 45.2 Epidemiology 45.3 Etiology and Pathogenesis 45.4 Systemic Manifestations 45.5 Ocular Manifestations 45.6 Manifestations in Immunocompromised Individuals 45.7 Complications 45.8 Diagnosis 45.9 Auxiliary Examinations 45.10 Differential Diagnosis 45.11 Treatment 45.12 Prognosis References 46: Ocular Toxocariasis 46.1 Definition 46.2 Epidemiology 46.3 Etiology and Pathogenesis 46.4 Clinical Manifestations 46.5 Diagnosis 46.6 Treatment 46.7 Prognosis References 47: Uveitis Associated with Human Immunodeficiency Virus 47.1 Definition 47.2 Epidemiology 47.3 Etiology and Pathogenesis 47.4 Systemic Manifestations 47.5 Ocular Disease 47.6 Diagnosis 47.7 Differential Diagnosis 47.8 Treatment References 48: Cytomegalovirus Retinitis 48.1 Definition 48.2 Epidemiology 48.3 Etiology and Pathogenesis 48.4 Systemic Diseases 48.5 Ocular Manifestations 48.6 Diagnosis 48.7 Differential Diagnosis 48.8 Treatment 48.9 Prognosis References 49: Acute Retinal Necrosis Syndrome 49.1 Definition 49.2 Epidemiology 49.3 Etiology and Pathogenesis 49.4 Clinical Manifestation 49.5 Complications 49.6 Diagnosis 49.7 Differential Diagnosis 49.8 Treatment 49.9 Prognosis References 50: Masquerade Syndrome 50.1 Overview 50.2 Intraocular Lymphoma 50.2.1 Definition 50.2.2 Epidemiology 50.2.3 Clinical Manifestations 50.2.4 Diagnosis 50.2.5 Differential Diagnosis 50.2.6 Treatment 50.2.7 Prognosis 50.3 Retinoblastoma (Rb) 50.3.1 Definition 50.3.2 Epidemiology 50.3.3 Clinical Manifestations 50.3.4 Diagnosis 50.3.5 Differential Diagnosis 50.3.6 Treatment 50.3.7 Prognosis 50.4 Leukemia 50.4.1 Definition 50.4.2 Clinical Manifestations 50.4.3 Diagnosis 50.4.4 Treatment 50.5 Uveal Melanoma 50.6 Metastasis to the Eye 50.6.1 Definition 50.6.2 Epidemiology 50.6.3 Clinical Manifestations 50.6.4 Diagnosis and Differential Diagnosis 50.6.5 Treatment References 51: Scleritis 51.1 Definition 51.2 Epidemiology 51.3 Etiology and Pathogenesis 51.4 Anterior Scleritis 51.5 Posterior Scleritis 51.6 Panscleritis 51.7 Complications 51.8 Diagnosis and Differential Diagnosis 51.9 Treatment 51.10 Prognosis References 52: Episcleritis 52.1 Definition 52.2 Epidemiology 52.3 Etiology and Pathogenesis 52.4 Clinical Manifestations 52.5 Treatment 52.6 Prognosis References