Description
Book SynopsisSome of the best clinical teaching happens during grand rounds, imaging conferences and the discussion of individual cases, but for ophthalmologists working in smaller centres, such opportunities can be infrequent. Handbook of Retinal Disease offers the benefit of a case discussion by describing retinal disorders through real-life examples, from a presenting problem through the differential diagnosis, an analysis of the imaging and other diagnostic results, to an outline treatment plan.
The book features over 80 cases, each presented with a table of signs and symptoms to help with the differential diagnosis, questions to ask the patient and relevant imaging to order. Secondly, imaging results from relevant modalities are discussed, before a final diagnosis is put forward. The authors provide concise information on the diagnosis, including an outline of recommended treatments, each one tailored to individual patients and reflecting the complex nature of some cases; follow-up and further reading.
With its high quality images and highly structured, deductive approach, this second edition provides a clinically relevant guide to the latest imaging techniques used in the diagnosis of retinal diseases: OCT, colour and red fundus photography, fluorescein and indocyanine green angiography and fundus autofluorescence.
The previous edition (9781907816925) published in 2015.
Table of ContentsSection 1: Normal retina
Chapter 1 Normal retina
Section 2: Retinal vascular disease
Chapter 2 Diabetic retinopathy
Chapter 3 Venous occlusive disease
Chapter 4 Arterial occlusive disease
Chapter 5 Retinal arterial macroaneurysm
Chapter 6 Roth spots
Chapter 7 Cotton wool spots
Chapter 8 Radiation retinopathy
Chapter 9 Hypertensive retinopathy
Chapter 10 Sickle cell retinopathy
Chapter 11 Ocular ischemic syndrome
Chapter 12 Papillophlebitis
Chapter 13 Macular telangiectasia and Coats’ disease
Chapter 14 Macular telangiectasia 2
Chapter 15 Retinopathy of prematurity
Section 3: Age-related macular degeneration and mimickers
Chapter 16 Dry age-related macular degeneration
Chapter 17 Wet (exudative) age-related macular degeneration
Chapter 18 Central serous chorioretinopathy
Chapter 19 Polypoidal chorioretinopathy
Chapter 20 Retinal angiomatous proliferation
Chapter 21 Pattern dystrophy
Chapter 22 Angioid streaks
Chapter 23 Myopic degeneration
Section 4: Vitreoretinal interface abnormalities and diseases of the vitreous
Chapter 24 Full-thickness macular hole
Chapter 25 Lamellar macular hole
Chapter 26 Vitreomacular traction syndrome
Chapter 27 Epiretinal membrane
Chapter 28 Macular pseudohole
Chapter 29 Posterior vitreous detachment
Chapter 30 Vitreous hemorrhage
Chapter 31 Asteroid hyalosis
Chapter 32 Cholesterolosis (synchisis scintillans)
Chapter 33 Persistent fetal vasculature
Section 5: Other macular disorders
Chapter 34 Hydroxychloroquine maculopathy
Chapter 35 Photic maculopathy
Chapter 36 Pentosan polysulfate toxic maculopathy
Chapter 37 Mitogen-activated protein kinase inhibitor toxic maculopathy
Section 6: Peripheral retinal pathology
Chapter 38 Retinal tear
Chapter 39 Retinal detachment
Chapter 40 Lattice degeneration
Section 7: Uveitis Infectious uveitis
Infectious uveitis
Chapter 41 Toxoplasmosis
Chapter 42 Cat scratch disease
Chapter 43 Cytomegalovirus retinitis
Chapter 44 Acute retinal necrosis
Chapter 45 Endophthalmitis
Chapter 46 Syphilitic chorioretinitis
Chapter 47 Tuberculosis
Chapter 48 Unilateral acute idiopathic maculopathy
Chapter 49 Presumed ocular histoplasmosis syndrome
Noninfectious uveitis
Chapter 50 Sarcoid
Chapter 51 Vitreoretinal lymphoma
Chapter 52 Multifocal evanescent white dot syndrome
Chapter 53 Acute multifocal placoid pigment epitheliopathy
Chapter 54 Acute macular neuroretinopathy
Chapter 55 Punctate inner choroidopathy
Chapter 56 Birdshot chorioretinopathy
Chapter 57 Intermediate uveitis
Chapter 58 Vogt–Koyanagi–Harada syndrome
Chapter 59 Behçet’s disease
Section 8: Hereditary retinal and choroidal dystrophies
Chapter 60 Retinitis pigmentosa
Chapter 61 Cone and cone–rod dystrophy
Chapter 62 Stargardt’s disease
Chapter 63 Autosomal recessive bestrophinopathy
Chapter 64 Choroidal dystrophies
Chapter 65 Oculocutaneous albinism
Chapter 66 X-linked retinoschisis
Chapter 67 Unilateral retinal pigment epithelium dysgenesis
Section 9: Neoplasms and focal lesions
Chapter 68 Choroidal nevus
Chapter 69 Choroidal melanoma
Chapter 70 Focal scleral nodules
Chapter 71 Scleral choroidal calcifications
Chapter 72 Choroidal osteoma
Chapter 73 Choroidal hemangioma
Chapter 74 Cavernous hemangioma
Chapter 75 Capillary hemangioma
Chapter 76 Combined hamartoma of the retina and retinal pigment epithelium
Chapter 77 Retinoblastoma
Chapter 78 Choroidal metastases
Section 10: Trauma
Chapter 79 Commotio retinae
Chapter 80 Choroidal rupture
Chapter 81 Valsalva retinopathy
Chapter 82 Purtscher’s retinopathy
Chapter 83 Intraocular foreign body
Chapter 84 Nonaccidental trauma (shaken baby syndrome)
Section 11: Surgical complications
Chapter 85 Silicone oil emulsification
Chapter 86 Retained perfluorocarbon
Chapter 87 Globe perforation from local anesthesia
Chapter 88 Suprachoroidal hemorrhage
