- •Preface
- •1: Anatomy and Physiology of the Retina
- •Pars Plana
- •Ora Serrata
- •Macula
- •Fovea, Foveola, and Umbo
- •Neurosensory Retina
- •Photoreceptors
- •Retinal Pigment Epithelium
- •Retinal Blood Flow
- •Choroid
- •Vitreous
- •Normal Retinal Adhesion
- •Blood-Retinal Barrier
- •Physiology of the Retina
- •Clinical Correlation: Retina
- •Clinical Correlation: Retinal Pigment Epithelium
- •Clinical Correlation: Vitreous, Retinal Adhesion, and Blood-Retinal Barrier
- •2: Ancillary Testing for Retinal and Choroidal Diseases
- •Fluorescein Angiography
- •Fluorescein Angiography: Hyperfluorescence
- •Fluorescein Angiography: Hypofluorescence
- •Indocyanine Green Angiography
- •Electroretinography
- •Electro-Oculography
- •Echography
- •Scanning Laser Ophthalmoscopy
- •Optical Coherence Tomography
- •3: Clinical Features of Retinal Disease
- •Cherry Red Spot
- •Chorioretinal Folds
- •Choroidal Neovascularization
- •Cotton Wool Spot
- •Cystoid Macular Edema
- •Drusen
- •Flecked Retina Syndromes
- •Foveal Yellow Spot
- •Intraretinal Hemorrhages
- •Lipid Exudates
- •Macular Atrophy
- •Optic Disc Edema With Macular Star
- •Peripheral Pigmentation
- •Pigmented Lesions
- •Preretinal Hemorrhage
- •Retinal Crystals
- •Retinal Neovascularization
- •Retinitis
- •Rubeosis
- •Tumors
- •Vasculitis
- •Vitelliform Lesions
- •Vitreous Hemorrhage
- •Vitreous Opacity
- •White Dot Syndromes
- •White-Centered Retinal Hemorrhages
- •4: Macular Diseases
- •Age-Related Macular Degeneration: Nonexudative
- •Age-Related Macular Degeneration: Exudative
- •Angioid Streaks
- •Central Serous Chorioretinopathy
- •Cystoid Macular Edema
- •Macular Hole
- •Myopic Degeneration
- •Pattern Dystrophy
- •Photic Retinopathy
- •5: Retinal Vascular Diseases
- •Branch Retinal Artery Occlusion
- •Branch Retinal Vein Occlusion
- •Central Retinal Artery Occlusion
- •Central Retinal Vein Occlusion
- •Hypertensive Retinopathy
- •Idiopathic Juxtafoveolar Retinal Telangiectasis
- •Leukemic Retinopathy
- •Ocular Ischemic Syndrome
- •Pregnancy-Related Retinal Disease
- •Radiation Retinopathy
- •Retinal Arterial Macroaneurysms
- •Retinopathy of Prematurity
- •Sickle Cell Retinopathy
- •6: Hereditary Retinal Disorders
- •Albinism
- •Choroideremia
- •Cone Dystrophies/Cone-Rod Dystrophies
- •Congenital Stationary Night Blindness
- •Dominant Drusen
- •North Carolina Macular Dystrophy
- •Retinitis Pigmentosa (Rod-Cone Dystrophies)
- •Stargardt Disease
- •7: Drug Toxicities
- •Aminoglycoside Toxicity
- •Crystalline Retinopathies
- •Iron Toxicity
- •Phenothiazine Toxicity
- •8: Intraocular Tumors
- •Choroidal Hemangioma
- •Choroidal Melanoma
- •Choroidal Metastasis
- •Choroidal Nevus
- •Choroidal Osteoma
- •Congenital Hypertrophy of the Retinal Pigment Epithelium
- •Intraocular Lymphoma
- •Melanocytoma
- •Phakomatoses: Neurofibromatosis
- •Phakomatoses: Sturge-Weber Syndrome
- •Phakomatoses: Tuberous Sclerosis
- •Phakomatoses: Von Hippel-Lindau Disease
- •Phakomatoses: Wyburn-Mason Syndrome
- •Retinoblastoma
- •9: Inflammatory Diseases
- •Acute Posterior Multifocal Placoid Pigment Epitheliopathy
- •Acute Retinal Necrosis
- •Cytomegalovirus Retinitis
- •Diffuse Unilateral Subacute Neuroretinitis
- •Endophthalmitis
- •Intermediate Uveitis
- •Multifocal Choroiditis and Panuveitis
- •Multiple Evanescent White Dot Syndrome
- •Neuroretinitis
- •Posterior Scleritis
- •Presumed Ocular Histoplasmosis Syndrome
- •Sarcoidosis
- •Syphilis
- •Systemic Lupus Erythematosus
- •Toxocariasis
- •Toxoplasmosis
- •Tuberculosis
- •Vogt-Koyanagi-Harada Syndrome
- •10: Trauma
- •Choroidal Rupture
- •Commotio Retinae
- •Optic Nerve Avulsion
- •Shaken Baby Syndrome
- •Valsalva Retinopathy
- •11: Peripheral Retinal Diseases
- •Cystic Retinal Tufts
- •Lattice Degeneration
- •Retinal Breaks
- •Retinal Detachment
- •Senile (Adult-Onset) Retinoschisis
- •12: Diseases of the Vitreous
- •Amyloidosis
- •Asteroid Hyalosis
- •Idiopathic Vitritis
- •Persistent Hyperplastic Primary Vitreous
- •Posterior Vitreous Detachment
- •Proliferative Vitreoretinopathy
- •Vitreous Hemorrhage
- •13: Histopathology of Retinal Diseases
- •Macular Diseases
- •Retinal Vascular Diseases
- •Intraocular Tumors
- •Inflammatory Diseases
- •Trauma
- •Peripheral Retinal Diseases
- •14: Clinical Trials in Retina
- •The Diabetic Retinopathy Study
- •The Early Treatment Diabetic Retinopathy Study
- •The Diabetic Retinopathy Vitrectomy Study
- •The Diabetes Control and Complications Trial
- •The Branch Vein Occlusion Study
- •The Central Vein Occlusion Study
- •The Multicenter Trial of Cryotherapy for Retinopathy of Prematurity
- •The Macular Photocoagulation Study
- •The Treatment of Age-Related Macular Degeneration With Photodynamic Therapy (TAP) Study
- •Branch Retinal Vein Occlusion: Macular Edema
- •Branch Retinal Vein Occlusion: Neovascularization
- •Central Serous Chorioretinopathy
- •Central Retinal Vein Occlusion
- •Choroidal Neovascularization
- •Diabetic Retinopathy: Clinically Significant Macular Edema
- •Diabetic Retinopathy: High-Risk Proliferative Diabetic Retinopathy
- •Peripheral Retinal Neovascularization
- •Retinal Arterial Macroaneurysm
- •Retinal Tears and Retinal Detachment
- •Retinal Telangiectasis and Retinal Angiomas
- •Photodynamic Therapy with Verteporfin
- •Index
248 |
C H A P T E R 9 Inflammatory Diseases |
ENDOPHTHALMITIS
Endophthalmitis refers to inflammation that may ultimately involve all tissues of the eye. Exogenous endophthalmitis occurs when trauma or surgery allows microorganisms access into the eye. Endogenous endophthalmitis occurs when microorganisms spread to the eye from another source in the body, usually via the bloodstream. Endophthalmitis is an infrequent clinical entity but has the potential to cause severe visual loss.
Symptoms
In postoperative and posttraumatic endophthalmitis, patients will notice increasing redness and decreasing vision within 1 to 7 days. Pain is usually but not necessarily present. The upper eyelid may become edematous and difficult to open. Discharge may be seen in the conjunctival cul-de-sac. In endogenous endophthalmitis, susceptible patients (eg, septic, immunocompromised, users of intravenous drugs) will notice progressively blurred vision or floaters. A chronic bacterial endophthalmitis following cataract surgery may masquerade as a chronic uveitis that occurs months to years following intraocular surgery.
Clinical Features
In exogenous endophthalmitis, ophthalmologic examination shows conjunctival injection and chemosis, variable degrees of corneal edema, anterior chamber cells, flare, fibrin, hypopyon, and heavy cellular debris in the vitreous. In endogenous endophthalmitis, examination shows vitreous cells and debris with either retinal involvement or a reduced red reflex. In chronic bacterial endophthalmitis caused by Propionibacterium acnes, a creamywhite plaque may be visible within the peripheral lens capsule.
Ancillary Testing
The clinical diagnosis is confirmed by obtaining aqueous and vitreous for culture on blood agar, chocolate agar, Sabouraud’s media or broth, and thioglycolate broth. Material is also placed on two glass slides for Gram and Giemsa stains. In post-traumatic endophthalmitis an orbital computed tomography scan is necessary to rule out an intraocular foreign body.
Pathology/Pathogenesis
Bacteria, fungi, protozoa, parasites, and viruses are all capable of producing endophthalmitis. The most common organisms causing acute bacterial endophthalmitis after cataract surgery are Staphylococcus aureus and
S epidermidis. Streptococcus pneumoniae and
Haemophilus influenzae are common causes of bacterial endophthalmitis following glaucoma filtering surgeries. In traumatic endophthalmitis, Bacillus species are frequent pathogens. Propionibacterium acnes is the most commonly recognized organism causing chronic bacterial endophthalmitis following cataract surgery.
Treatment/Prognosis
Intravitreal injection of antibiotics, with or without victrectomy, is the standard of care in endophthalmitis. Antibiotics can also be administered via systemic, periocular, and topical routes. The role of corticosteroids remains controversial. Regarding visual outcome, the most important prognostic indicator is the virulence of the infecting organism. Although the use of prophylactic antibiotics to reduce the occurrence of post-cataract surgery endophthalmitis is controversial, most surgeons recommend using preoperative povidone-iodine antisepsis.
Systemic Evaluation
Systemic evaluation is generally not necessary for exogenous endophthalmitis. For endogenous endophthalmitis, an aggressive search for the systemic source of infection is indicated, including cultures of the blood, urine, indwelling catheters, and intravenous lines. Involvement of an infectious disease specialist or internist is essential.
C H A P T E R 9 Inflammatory Diseases |
249 |
|
|
|
|
|
|
|
Acute bacterial endophthalmitis following cataract surgery is characterized by conjunctival injection and chemosis, corneal edema, anterior chamber cell and flare, and hypopyon. The degree of pain is variable.
Endophthalmitis may develop in patients following glaucoma filtering surgery, with or without the use of topical antimetabolites. Common bacteria include
Streptococcus pneumoniae and Haemophilus influenzae.
Some patients with acute bacterial endophthalmitis have fibrin in the pupil in addition to the hypopyon. Common organisms include Staphylococcus aureus and
S epidermidis.
This patient developed endophthalmitis following a penetrating corneal injury. Bacillus species are common causes of traumatic endophthalmitis.
Propionibacterium acnes is the most commonly recognized organism causing chronic bacterial endophthalmitis following cataract surgery. P acnes endophthalmitis may mimic chronic uveitis.
Retroillumination of the same eye reveals the shadow of a capsular plaque in the 9 o’clock position. The patient responded well to pars plana vitrectomy and intraocular vancomycin.
Return to Quiz
250 |
C H A P T E R 9 Inflammatory Diseases |
HUMAN IMMUNODEFICIENCY VIRUS RETINOPATHY
Human immunodeficiency virus (HIV) is a retrovirus implicated in the development of acquired immunodeficiency syndrome (AIDS). Infection of helper T cells results in a profound disruption of the cell-mediated immune system. Immunodeficiency leads to susceptibility to blinding infections.
Symptoms
Pathology/Pathogenesis
Cotton wool spots result from microinfarction of the nerve fiber layer. Arteriolar deposition of immunoglobulin in the microvasculature around the cotton wool spots suggests an immune complex disease. Attempts to isolate organisms from cotton wool spots have been unsuccessful.
Noninfectious retinopathy is generally asymptomatic. Symptomatic disease is most often secondary to infectious disease occurring with the development of AIDS.
Clinical Features
The most common finding is a noninfectious retinopathy characterized by cotton wool spots, retinal hemorrhages, and microvascular disease. The noninfectious retinopathy does not correlate with the clinical severity of HIV disease. Chorioretinal infectious disease associated with AIDS includes cytomegalovirus retinitis, toxoplasmosis,
Mycobacterium avium-intracellulare choroiditis, cryptococcus choroiditis, and Pneumocystis carinii choroiditis.
Ancillary Testing
Human immunodeficiency virus retinopathy does not require other testing.
Treatment/Prognosis
Noninfectious HIV retinopathy does not require treatment. While some investigators have speculated that cotton wool spots may represent P carinii infection or early cytomegalovirus retinopathy, patients with noninfectious HIV retinopathy should not be subjected to toxic medications. Infectious retinopathy must be aggressively treated.
Systemic Evaluation
The diagnosis of HIV must be considered in patients with unexplained cotton wool spots or intraretinal hemorrhages. Patients with HIV disease or AIDS must be followed up closely by internists or infectious disease specialists for the many systemic diseases associated with immunodeficiency.
C H A P T E R 9 Inflammatory Diseases |
251 |
|
|
|
|
|
|
|
Fundus photograph of a 39-year-old man with human immunodeficiency virus (HIV) disease reveals numerous cotton wool spots and intraretinal hemorrhages characteristic of HIV retinopathy.
Cytomegalovirus retinitis is the most common opportunistic ocular infection in patients with acquired immunodeficiency syndrome. Cytomegalovirus retinitis is characterized by full-thickness retinitis and intraretinal hemorrhage.
Higher-magnification view of same patient reveals cotton wool spots and intraretinal hemorrhages. A few of the intraretinal hemorrhages have white centers.
Patients with acquired immunodeficiency syndrome may develop toxoplasmosis retinochoroiditis. The extent of vitritis is low because of the immunodeficiency. Patients may develop diffuse infection with acute retinal necrosis.
Pneumocystis carinii choroiditis was seen in patients with acquired immunodeficiency syndrome before the use of systemic therapy. Patients were usually asymptomatic in spite of the dramatic appearance of the choroidal lesions.
Progressive outer retinal necrosis is a form of acute retinal necrosis seen in patients with acquired immunodeficiency syndrome. It is characterized by full-thickness retinitis without evidence of intraocular inflammation or vasculitis.
